US20070043289A1 - Method and Apparatus Including Use of Metalloporphyrins for Subsequent Optimization of Radiosurgery and Radiotherapy - Google Patents
Method and Apparatus Including Use of Metalloporphyrins for Subsequent Optimization of Radiosurgery and Radiotherapy Download PDFInfo
- Publication number
- US20070043289A1 US20070043289A1 US11/532,021 US53202106A US2007043289A1 US 20070043289 A1 US20070043289 A1 US 20070043289A1 US 53202106 A US53202106 A US 53202106A US 2007043289 A1 US2007043289 A1 US 2007043289A1
- Authority
- US
- United States
- Prior art keywords
- patient
- target region
- mapping
- tissue
- pet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000002673 radiosurgery Methods 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title abstract description 39
- 238000001959 radiotherapy Methods 0.000 title abstract description 17
- 238000005457 optimization Methods 0.000 title abstract description 4
- 238000013507 mapping Methods 0.000 claims abstract description 33
- 230000005855 radiation Effects 0.000 claims abstract description 23
- 230000004044 response Effects 0.000 claims abstract description 4
- 238000002603 single-photon emission computed tomography Methods 0.000 claims abstract 7
- 239000011572 manganese Substances 0.000 claims description 17
- 230000001678 irradiating effect Effects 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 11
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
- 230000001338 necrotic effect Effects 0.000 claims description 4
- ULERISLJYQKABB-UHFFFAOYSA-N C1=CC(S(=O)(=O)O)=CC=C1C1=CC2=CC([N]3)=CC=C3C=C(C=C3)NC3=CC([N]3)=CC=C3C=C1N2 Chemical compound C1=CC(S(=O)(=O)O)=CC=C1C1=CC2=CC([N]3)=CC=C3C=C(C=C3)NC3=CC([N]3)=CC=C3C=C1N2 ULERISLJYQKABB-UHFFFAOYSA-N 0.000 claims description 3
- 238000013500 data storage Methods 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 230000004913 activation Effects 0.000 claims 6
- 238000012831 peritoneal equilibrium test Methods 0.000 claims 4
- 238000012636 positron electron tomography Methods 0.000 claims 4
- 238000012877 positron emission topography Methods 0.000 claims 4
- 238000012879 PET imaging Methods 0.000 claims 1
- 238000011282 treatment Methods 0.000 abstract description 26
- 230000003211 malignant effect Effects 0.000 abstract description 9
- 230000009977 dual effect Effects 0.000 abstract 1
- 210000001519 tissue Anatomy 0.000 description 56
- 206010028980 Neoplasm Diseases 0.000 description 40
- 150000004032 porphyrins Chemical class 0.000 description 19
- 238000002600 positron emission tomography Methods 0.000 description 19
- 230000002285 radioactive effect Effects 0.000 description 14
- 201000011510 cancer Diseases 0.000 description 13
- 239000010949 copper Substances 0.000 description 12
- 210000004027 cell Anatomy 0.000 description 10
- 238000003384 imaging method Methods 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 238000002591 computed tomography Methods 0.000 description 9
- 238000002595 magnetic resonance imaging Methods 0.000 description 8
- 238000001514 detection method Methods 0.000 description 5
- 230000001613 neoplastic effect Effects 0.000 description 5
- 238000012216 screening Methods 0.000 description 5
- KSFOVUSSGSKXFI-GAQDCDSVSA-N CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O Chemical compound CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O KSFOVUSSGSKXFI-GAQDCDSVSA-N 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- PBHVCRIXMXQXPD-UHFFFAOYSA-N chembl2369102 Chemical compound C1=CC(S(=O)(=O)O)=CC=C1C(C1=CC=C(N1)C(C=1C=CC(=CC=1)S(O)(=O)=O)=C1C=CC(=N1)C(C=1C=CC(=CC=1)S(O)(=O)=O)=C1C=CC(N1)=C1C=2C=CC(=CC=2)S(O)(=O)=O)=C2N=C1C=C2 PBHVCRIXMXQXPD-UHFFFAOYSA-N 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 238000002428 photodynamic therapy Methods 0.000 description 4
- -1 porphyrin compounds Chemical class 0.000 description 4
- 229950003776 protoporphyrin Drugs 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZGXJTSGNIOSYLO-UHFFFAOYSA-N 88755TAZ87 Chemical compound NCC(=O)CCC(O)=O ZGXJTSGNIOSYLO-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- 229960002749 aminolevulinic acid Drugs 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000001917 fluorescence detection Methods 0.000 description 3
- 230000003902 lesion Effects 0.000 description 3
- 230000004807 localization Effects 0.000 description 3
- 230000036210 malignancy Effects 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 206010039897 Sedation Diseases 0.000 description 2
- 238000001574 biopsy Methods 0.000 description 2
- 210000002798 bone marrow cell Anatomy 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 230000003915 cell function Effects 0.000 description 2
- 238000002512 chemotherapy Methods 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000002872 contrast media Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 210000004072 lung Anatomy 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 230000036244 malformation Effects 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- 230000036280 sedation Effects 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 210000004881 tumor cell Anatomy 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- UJKPHYRXOLRVJJ-MLSVHJFASA-N CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C Chemical class CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C UJKPHYRXOLRVJJ-MLSVHJFASA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 229910052765 Lutetium Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 206010040914 Skin reaction Diseases 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052769 Ytterbium Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 230000004856 capillary permeability Effects 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-IGMARMGPSA-N copper-64 Chemical compound [64Cu] RYGMFSIKBFXOCR-IGMARMGPSA-N 0.000 description 1
- RYGMFSIKBFXOCR-AKLPVKDBSA-N copper-67 Chemical compound [67Cu] RYGMFSIKBFXOCR-AKLPVKDBSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 238000002695 general anesthesia Methods 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000013152 interventional procedure Methods 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- OHSVLFRHMCKCQY-UHFFFAOYSA-N lutetium atom Chemical compound [Lu] OHSVLFRHMCKCQY-UHFFFAOYSA-N 0.000 description 1
- 230000001926 lymphatic effect Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000037323 metabolic rate Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000005087 mononuclear cell Anatomy 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000013421 nuclear magnetic resonance imaging Methods 0.000 description 1
- 238000011275 oncology therapy Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 208000017983 photosensitivity disease Diseases 0.000 description 1
- 231100000434 photosensitization Toxicity 0.000 description 1
- 238000001126 phototherapy Methods 0.000 description 1
- 231100000760 phototoxic Toxicity 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 239000012217 radiopharmaceutical Substances 0.000 description 1
- 229940121896 radiopharmaceutical Drugs 0.000 description 1
- 230000002799 radiopharmaceutical effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 231100000430 skin reaction Toxicity 0.000 description 1
- 230000035483 skin reaction Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229940127044 therapeutic radiopharmaceutical Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium(II) oxide Chemical compound [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000003325 tomography Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- IBYSTTGVDIFUAY-UHFFFAOYSA-N vanadium monoxide Chemical compound [V]=O IBYSTTGVDIFUAY-UHFFFAOYSA-N 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/0474—Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group
- A61K51/0485—Porphyrins, texaphyrins wherein the nitrogen atoms forming the central ring system complex the radioactive metal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/12—Arrangements for detecting or locating foreign bodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/001—Preparation for luminescence or biological staining
- A61K49/0013—Luminescence
- A61K49/0017—Fluorescence in vivo
- A61K49/0019—Fluorescence in vivo characterised by the fluorescent group, e.g. oligomeric, polymeric or dendritic molecules
- A61K49/0021—Fluorescence in vivo characterised by the fluorescent group, e.g. oligomeric, polymeric or dendritic molecules the fluorescent group being a small organic molecule
- A61K49/0036—Porphyrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
- A61N5/1048—Monitoring, verifying, controlling systems and methods
- A61N5/1049—Monitoring, verifying, controlling systems and methods for verifying the position of the patient with respect to the radiation beam
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5091—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing the pathological state of an organism
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04N—PICTORIAL COMMUNICATION, e.g. TELEVISION
- H04N23/00—Cameras or camera modules comprising electronic image sensors; Control thereof
- H04N23/50—Constructional details
- H04N23/54—Mounting of pick-up tubes, electronic image sensors, deviation or focusing coils
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04N—PICTORIAL COMMUNICATION, e.g. TELEVISION
- H04N23/00—Cameras or camera modules comprising electronic image sensors; Control thereof
- H04N23/50—Constructional details
- H04N23/555—Constructional details for picking-up images in sites, inaccessible due to their dimensions or hazardous conditions, e.g. endoscopes or borescopes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
- A61N5/1048—Monitoring, verifying, controlling systems and methods
- A61N5/1049—Monitoring, verifying, controlling systems and methods for verifying the position of the patient with respect to the radiation beam
- A61N2005/1061—Monitoring, verifying, controlling systems and methods for verifying the position of the patient with respect to the radiation beam using an x-ray imaging system having a separate imaging source
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
- A61N5/1048—Monitoring, verifying, controlling systems and methods
- A61N5/1064—Monitoring, verifying, controlling systems and methods for adjusting radiation treatment in response to monitoring
- A61N5/1065—Beam adjustment
- A61N5/1067—Beam adjustment in real time, i.e. during treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/968—High energy substrates, e.g. fluorescent, chemiluminescent, radioactive
Definitions
- This invention relates to cancer screening and cancer treatment, and more particularly, to the use of metalloporphyrins for subsequent optimization of radiosurgery and/or radiotherapy.
- Fluorescent markers have been used to help identify cancerous tissue within a patient.
- Radio tracers or markers have also been used in the detection and treatment of cancer.
- U.S. Pat. No. 5,391,547 discloses a method of using porphyrins to detect lung cancer, and more particularly, to the use of tetra-aryl porphyrins.
- the porphyrins are used as a fluorescent tracer for cancers of the lung.
- the porphyrins may be complexed with Copper 64 ( 64 Cu) or Copper 67 ( 67 Cu).
- 64 Cu Copper 64
- 67 Cu Copper 67
- the 67 Cu provides a source of beta radiation for selective destruction of lung malignancies as well as gamma radiation useful for image analysis, as by single photon emission computer tomography.
- the 64 Cu may be used for radio tracing wherein a positron emission tomography technique can be used to locate the malignant tissue.
- U.S. Pat. No. 5,087,636 to Jamieson, et al. discloses a method to identify and destroy malignant cells in mononuclear cell populations. This method includes the steps of contacting a composition of bone marrow cells or other cells with a green porphyrin of a specific compound, irradiating the cell composition with light at a wave length effective to excite fluorescence of the green porphyrin, and then detecting the presence or absence of fluorescence indicating malignancy.
- This reference also discloses the steps by which the bone marrow cells are removed, separated, washed and diluted to an appropriate concentration for treatment, incubated, centrifuged, and exposed to the irradiating light.
- U.S. Pat. Nos. 5,308,608 and 5,149,708 to Dolphin, et al. disclose specific types of porphyrin compounds which may be used for detection, photosensitization, or the destruction of a targeted biological material when the targeted tissue is contacted with the specified porphyrin, and irradiated with light that excites the compound.
- U.S. Pat. No. 5,211,938 to Kennedy, et al. discloses a method of detection of malignant and non-malignant lesions by photo chemotherapy of protoporphyrin IX precursors.
- 5-amino levulinic acid (5-ALA) is administered to the patient in an amount sufficient to induce synthesis of protoporphyrin IX in the lesions, followed by exposure of the treated lesion to a photo activating light in the range of 350-640 nanometers.
- Naturally-occurring protoporphyrin IX is activatable by light which is in the incident red light range (600-700 nanometers) which more easily passes through human tissue as compared to light of other wave lengths which must be used with other types of porphyrins.
- 5-ALA makes cell fluorescence easier to observe, and also greatly reduces the danger of accidental phototoxic skin reactions in the days following treatment since protoporphyrin IX precursors have a much shorter half life in normal tissues than other popularly used porphyrins.
- interventional devices such as endoscopes which have the special capability of delivering specified light frequencies to a targeted tissue of a patient. These endoscopes illuminate the targeted part of the body in which cancer is suspected. The light delivered at a specified frequency illuminates an area which has previously been subjected to some type of fluorescent marker, such as a porphyrin which causes malignant cells to illuminate or fluoresce under observation of light at the specified frequency. In all cases, introduction of an endoscope into the body requires some type of sedation or general or local anesthesia. Once a tumor has been located by use of the interventional device, depending upon the type of tumor, photo chemotherapy or other treatment means can be used.
- Stereotaxic radio surgery is a well known procedure to treat tumorous tissue. This type of radio surgery is particularly well known for treating brain tumors. Advances in technology for delivering a collimated surgical ionizing beam now allows medical personnel to treat patients with cancerous tissue throughout the body.
- One company that provides a stereotaxic radio surgery system is Accuray of Boulder, Colo.
- One system developed by Accuray includes the CyberknifeTM system that incorporates a linear accelerator mounted on a robotic arm thereby providing a surgeon with great flexibility in delivering a collimated beam to a targeted area.
- the Cyberknife has been used to radiosurgically treat many tumors and other malformations at body sites which are unreachable by other stereotaxic systems.
- U.S. Pat. No. 5,207,223 discloses a method and apparatus for selectively irradiating a target within a patient.
- a 3-dimensional mapping is provided of a region surrounding the target.
- a beaming apparatus emits a collimated beam. Diagnostic beams at a known non-zero angle to one another pass through the mapping region. Images of projections are produced within the mapping region. Electronic representations of the images are compared with reference data from the 3-dimensional mapping thereby locating the target.
- the relative positions of the beaming apparatus and the living organism are adjusted in such a manner that the collimated beam is focused on the target region despite any movement by the patient during treatment.
- a comparison is repeated at small time intervals and, when the comparison so indicates, adjustment is repeated, as needed, and in such a manner that the collimated beam remains focused on the target region.
- U.S. Pat. No. 5,427,097 owned by Accuracy discloses another apparatus and method of performing stereotaxic surgery.
- a robotic arm and beam generating arrangement are provided along a predetermined, non-circular and non-linear path transverse to a collimated beam path, while at the same time, the collimated beam path is directed into the target region.
- the radiosurgical/radiotheraputic beam can be directed through the target region from particular treatment points along the transverse path so as to define a non-spherical target region, thereby allowing treatment of irregularly shaped tumors or malformations.
- One important objective of the inventions disclosed in these references owed by Accuracy is to improve the ability to deliver a radiological beam which can be precisely targeted for irradiating targeted tissue, yet limiting exposure of healthy tissue. With the inventions disclosed in the two references, it is possible to perform multiple fraction radiological treatment thereby improving the ability to target and localize cancerous or malformed tissue.
- 3-dimensional mapping is obtained by a CAT scan (CT) or by magnetic resonance imaging (MRI).
- CT CAT scan
- MRI magnetic resonance imaging
- computerized tomography operates through measurement of the differential absorption of x-ray beams, and the resulting images are in the form of data which is mathematically manipulated through Fourier transform.
- MRI utilizes nuclear magnetic resonance properties of tissue to obtain 3-dimensional mapping.
- CT scanners and MRI scanners are available commercially, and the data obtained by the scanning can be placed in a digitized format whereby it can be stored and manipulated through software in a computer.
- an MRI or CT scan may be adequate under many circumstances, the disadvantages of CT scanning or MRI scanning is that these types of scans image the physical structure of tissue, and do not provide information regarding the body's chemistry, or cell function.
- PET positron emission tomography
- CT computed tomography
- MRI magnetic resonance imaging
- PET typically involves the administration of a radioactive form of glucose, and then the PET scanner tracks and records signals which are emitted by the administered compound. Actively growing cancer cells typically have much higher metabolic rates than normal cells; therefore, the radioactive glucose is metabolized more quickly by these cancerous tissues, thereby creating distinct signals which can be recorded by the PET scanner.
- a computer then reconstructs the recorded signals into 3-dimensional digital images that show areas throughout the body where diseases are present.
- SPECT single photon emission computer tomography
- SPECT single photon emission computer tomography
- SPECT scanning a small amount of a radioactive isotope is administered to a patient, and any increased metabolic activity present at various body locations can be identified and reviewed to determine whether a patient has diseased or cancerous tissue.
- porphyrins One class of chemicals useful for the treatment of tumors is the porphyrins and particularly hematoporphyrin derivatives. These chemicals have been studied as a result of their selective localization and uptake into tumors and malignant tissue and their sensitization of tumor tissues to photoirradiation. It has also been suggested that these chemicals could function as delivery vehicles to target other anticancer compounds to tumor tissues due to their selective uptake into tumor tissues.
- porphyrin molecules may chelate one of many different metal atoms which are then localized to tumor tissues. These metal atoms can be radioactive isotopes which then irradiate the surrounding tumor tissue after localization to the tumor within a metalloporphyrin.
- the radioactivity emitted can be used in PET or SPECT scanning to create an image of the tumor tissue.
- the metalloporphyrins are still effective in selectively delivering a metal atom to tumor tissues.
- the metal can then act as a contrast agent to enhance magnetic resonance imaging or nuclear magnetic resonance imaging. Because the localization of the metalloporphyrins is based on the chemical properties of the porphyrins themselves and their interaction with characteristics of tumor cells including large interstitial space, high capillary permeability and lack of lymphatic drainage, and not on differences in metabolic activities in tissues, they are more selectively taken up and retained by malignant cells than are radioactive glucose molecules. For this reason, the metalloporphyrins are also better contrast agents for use with the different tumor imaging techniques than are radioactive glucose molecules.
- the present invention provides a method and apparatus including use of metalloporphyrins for subsequent optimization of radio surgery and radio therapy.
- the present invention may make use of porphyrin compounds complexed with various metals such as silver (Ag), aluminum (Al), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), gadolinium (Gd), indium (In), lutetium (Lu), magnesium (Mg), manganese (Mn), nickel (Ni), palladium (Pd), platinum (Pt), rhodium (Rh), ruthenium (Ru), scandium (Sc), silicon (Si), tin (Sn), titanium oxide (TiO), vanadium oxide (VO), ytterbium (Yb) and zinc (Zn).
- various metals such as silver (Ag), aluminum (Al), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), gadolinium (Gd), indium (In), lutetium (Lu), magnesium (Mg), manganese (
- metalloporphyrins meaning a porphyrin moiety having a chelated radioactive isotope of a metal atom.
- metalloporphyrins are further processed so that the metal is in the form of a radioactive isotope.
- the resulting radioactive metalloporphyrins thereby constitute radiopharmaceuticals that can be intravenously introduced to the patient.
- the affinity of neoplastic tissue for porphyrins results in selective uptake of the radioactive metalloporphyrin, thereby effecting targeted delivery of therapeutic radiopharmaceuticals.
- the copper can be transformed to radioactive 67 Cu.
- metalloporphyrin radiopharmacuetical introduction of the metalloporphyrin radiopharmacuetical to the patient is an effective means to deliver measured radiation therapy to targeted tissue.
- 67 Cu provides a source of beta radiation for selective destruction of neoplastic sites.
- metalloporphyrin complexes still provide the ability to simultaneously conduct fluorescence detection and phototherapy if desired.
- the metalloporphyrins provide the ability for observation of the targeted areas through PET (for example, through the use of 64 Cu) or SPECT (for example, through use the of 67 Cu).
- a selected group of porphyrin compounds complexed with various metals are specifically contemplated in the present invention because these metalloporphyrins are particularly effective in tumor tissue imaging.
- the synthetic water soluble porphyrins which contain hydrophilic groups peripheral to the porphyrin ring facilitate oral administration and avoid the use of additional solubilizing agents.
- Fe (III) and Mn (III) meso-tetra (4-sulfonatophenyl) porphine (TPPS 4 ) are water soluble metalloporphyrins that show an increased affinity for solid tumor cells. This affinity is higher than would be expected for the metalloporphyrins as a general class of compounds.
- Iron is known to have seven radioisotopes ( 52 Fe, 53 Fe, 55 Fe, 59 Fe, 60 Fe, 61 Fe, 62 Fe) and manganese is known to have six radioisotopes ( 51 Mn, 52 Mn, 53 Mn, 54 Mn, 55 Mn, 56 Mn, 57 Mn) providing many radioisotopes that can be used in the TPPS 4 prophyrin molecule.
- Each of these isotopes can be selected for the desired characteristics in terms of half life and emission spectra that make for the best use in producing, shipping and using the radioisotope in the scanning procedure. For example, 59 Fe has a half life about 44.5 days while 62 Fe has a half life of about 68 seconds.
- the desired radioisotope of these two metal atoms can be selected depending on the photon emission characteristics and a suitable or desired half-life.
- Table I contains a list of the radioisotopes of these two metal atoms and their half-lives. Therefore, the Fe (III) and Mn (III) derivatives of TPPS 4 having a radiometal capable of photo emission are preferred metalloporphyrins for use in the radiosurgery imaging techniques of the present invention.
- the desired metalloporphyrin may be administered directly to the patient orally, topically, or intravenously.
- a particular waiting period is necessary for uptake of the porphyrin compound.
- a cancer screening procedure may take place wherein the patient is subject to an initial PET or SPECT procedure, and either a particular location may be imaged, or the entire body may be imaged, for example, to determine the extent to which a tumor has metastasized.
- 3-dimensional images of targeted body locations are created through mapping and the images are stored in a computer.
- the particular stereotaxic radiosurgery procedure that is contemplated is the same as that disclosed in the above-mentioned U.S. Pat. Nos. 5,207,223 and 5,427,097, these references being incorporated herein by reference in their entireties.
- the present invention differs from the procedures disclosed in these prior art references by the method in which tissue is imaged. Instead of a CAT scan or MRI scan, 3-dimensional mapping is achieved by PET or SPECT scanning.
- a beaming apparatus is provided to generate a collimated surgical ionizing beam of a sufficient strength to cause a targeted region to become necrotic.
- a preferred beaming apparatus includes an x-ray linear accelerator, although other ionizing radiation sources can be used. Means are provided which allow the collimated beam to be precisely aligned with the targeted area through a comparison of imaging data which takes place in real-time during treatment and the previously mapped images.
- the imaging which takes place during the treatment according to the present invention also includes imaging achieved by PET or SPECT.
- a metalloporphyrin is again administered to the patient prior to the treatment, and the metalloporphyrin metabolized in neoplastic tissue allows a very distinct target by which the collimated beam can be aligned. Images which are obtained real-time during treatment are compared with the previous mapped images, and the collimated beam is adjusted as necessary to maintain the collimated beam in alignment with its targeted location.
- the metalloporphyrin can be specifically formulated to provide a desired amount of radiation which will not only allow 3-dimensional mapping during a PET/SPECT scanning, but may also provide radiation for treatment by exposure of the suspect tissue during the time in which the metalloporphyrin is metabolized by the tissue.
- the later radiosurgical procedure by use of an irradiating beam can be dosed to provide the amount of radiation necessary to provide the additional treatment necessary. Accordingly, the initial exposure of the tissue to the metalloporphyrin may result in desired treatment to a specific level, and the remaining required treatment can then be provided by the irradiating beam.
- the present invention has great flexibility in delivering radiation in two separate ways, namely, the administration of the metalloporphyrin and the use of an irradiating beam. If two administrations of a metalloporphyrin are required (i.e., once for mapping and once for providing real-time images), then the administrations are collectively dosed to deliver the desired amount of radiation.
- radiosurgery/radiotherapy can be optimized in a manner which enhances the ability to provide a radiosurgical beam to targeted areas in the body and to limit the adverse effects of radiation exposure of healthy tissue.
- FIG. 1 is a block diagram illustrating the major components enabling completion of the method of the present invention.
- a system for delivering a collimated ionizing beam of radiation to a targeted area of tissue.
- Examples of such systems to support the present invention are disclosed in the U.S. Pat. Nos. 5,427,097 and 5,207,223.
- a representative system to achieve the present invention includes a computer 10 with data storage capability that is capable of executing instructions from software loaded within the computer.
- the computer can store and manipulate 3-dimensional mapping data images 12 of a patient being treated.
- the 3-dimensional mapping is typically stored in digital form, and is loaded in the computer 10 for later comparison purposes.
- the 3-dimensional mapping is preferably achieved by SPECT or PET scanning following administration of a metaloporphyrin to a patient.
- a beaming apparatus 16 is provided which, when activated, emits a collimated surgical ionizing beam of a sufficient strength to cause a targeted region to become necrotic.
- Means are provided for generating real-time images 14 of tissue at and around the area which is being treated by the collimated beam during the stereotaxic radiosurgery/radiotherapy.
- the real-time images may be created by passing first and second diagnostic beams through the mapping region, the beams being laterally extensive to provide projections of the mapping region such as disclosed in the U.S. Pat. No. 5,207,223.
- the preferred manner in which to provide real-time images for comparison of the previous 3-dimensional mapping is to conduct an additional PET or SPECT procedure.
- the collimated beam can be better controlled, and the strength and duration of the beam can be minimized to provide only the amount of radiation necessary to treat targeted tissue, thereby minimizing exposure of healthy tissue to the radiation.
- such treatment can be provided without having to use fiducials or other markers since the metalloporphyrins will efficiently localize in cancerous tissue, and the images are of such high quality that apparatuses such as a fiducials are therefore unnecessary to provide reference points to help locate suspect areas.
- Radiation therapy can be delivered to a patient in the present method in multiple ways.
- the initial administration of the metalloporphyrin may have significant therapeutic results, and stereotaxic radiation can then complete the necessary radiation treatment.
- the dosages of radiation provided both by the metalloporphyrin and the irradiating beam can be selectively adjusted to provide the desired level of treatment.
- use of the irradiating beam to treat suspect tissue can be better delivered to the patient because PET/SPECT precisely images suspect tissue.
- the irradiating beam can thereby be better aligned and minimized in strength and duration to irradiate only the target region thereby minimizing exposure of healthy tissue that surrounds the suspect tissue.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Urology & Nephrology (AREA)
- Pathology (AREA)
- Hematology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Cell Biology (AREA)
- Medical Informatics (AREA)
- Optics & Photonics (AREA)
- Epidemiology (AREA)
- Radiology & Medical Imaging (AREA)
- Food Science & Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Signal Processing (AREA)
- Multimedia (AREA)
- Biophysics (AREA)
- Hospice & Palliative Care (AREA)
- Pharmacology & Pharmacy (AREA)
- Physiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- High Energy & Nuclear Physics (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Surgery (AREA)
Abstract
An apparatus and method for subsequent optimization of radiosurgery and radiotherapy is provided. The invention includes administering a metalloporphyrin to the patient, and then creating a 3-dimensional mapping of tissue through use of PET or SPECT. Malignant and pre-malignant tissue has an affinity for the metalloporphyrin. During treatment, real-time images are also provided which are compared to the previous 3-dimensional mapping. Creation of the real-time images is also achieved through PET or SPECT wherein a metalloporphyrin is administered to the patient. Total administration of radiation is calculated by summing radiation from the inetalloporphyrins and from the radiosurgery/radiotherapy. The amount of radiation delivered by the metalloporphyrins and by the radiosurgery/radiotherapy are adjustable based on a patient's response to the dual delivery.
Description
- This application is a continuation-in-part of co-application Ser. No. 10/176,558, filed on Jun. 21, 2002, entitled “METHOD OF CANCER SCREENING PRIMARILY UTILIZING NON-INVASIVE CELL COLLECTION, FLUORESCENCE DETECTION TECHNIQUES, AND RADIO TRACING DETECTION TECHNIQUES”, the disclosure of which is hereby incorporated by reference herein.
- This invention relates to cancer screening and cancer treatment, and more particularly, to the use of metalloporphyrins for subsequent optimization of radiosurgery and/or radiotherapy.
- There are a number of prior art methods and apparatuses which are used in the detection and treatment of cancer. Fluorescent markers have been used to help identify cancerous tissue within a patient. Radio tracers or markers have also been used in the detection and treatment of cancer.
- U.S. Pat. No. 5,391,547 discloses a method of using porphyrins to detect lung cancer, and more particularly, to the use of tetra-aryl porphyrins. The porphyrins are used as a fluorescent tracer for cancers of the lung. The porphyrins may be complexed with Copper 64 (64Cu) or Copper 67 (67Cu). Thus, the complex can be used as radio tracers as well. The 67Cu provides a source of beta radiation for selective destruction of lung malignancies as well as gamma radiation useful for image analysis, as by single photon emission computer tomography. The 64Cu may be used for radio tracing wherein a positron emission tomography technique can be used to locate the malignant tissue.
- U.S. Pat. No. 5,087,636 to Jamieson, et al. discloses a method to identify and destroy malignant cells in mononuclear cell populations. This method includes the steps of contacting a composition of bone marrow cells or other cells with a green porphyrin of a specific compound, irradiating the cell composition with light at a wave length effective to excite fluorescence of the green porphyrin, and then detecting the presence or absence of fluorescence indicating malignancy. This reference also discloses the steps by which the bone marrow cells are removed, separated, washed and diluted to an appropriate concentration for treatment, incubated, centrifuged, and exposed to the irradiating light.
- U.S. Pat. Nos. 5,308,608 and 5,149,708 to Dolphin, et al. disclose specific types of porphyrin compounds which may be used for detection, photosensitization, or the destruction of a targeted biological material when the targeted tissue is contacted with the specified porphyrin, and irradiated with light that excites the compound.
- U.S. Pat. No. 5,211,938 to Kennedy, et al. discloses a method of detection of malignant and non-malignant lesions by photo chemotherapy of protoporphyrin IX precursors. 5-amino levulinic acid (5-ALA) is administered to the patient in an amount sufficient to induce synthesis of protoporphyrin IX in the lesions, followed by exposure of the treated lesion to a photo activating light in the range of 350-640 nanometers. Naturally-occurring protoporphyrin IX is activatable by light which is in the incident red light range (600-700 nanometers) which more easily passes through human tissue as compared to light of other wave lengths which must be used with other types of porphyrins. In short, the use of 5-ALA makes cell fluorescence easier to observe, and also greatly reduces the danger of accidental phototoxic skin reactions in the days following treatment since protoporphyrin IX precursors have a much shorter half life in normal tissues than other popularly used porphyrins.
- Present methods relating to cancer screening using fluorescence detection systems require the use of interventional devices such as endoscopes which have the special capability of delivering specified light frequencies to a targeted tissue of a patient. These endoscopes illuminate the targeted part of the body in which cancer is suspected. The light delivered at a specified frequency illuminates an area which has previously been subjected to some type of fluorescent marker, such as a porphyrin which causes malignant cells to illuminate or fluoresce under observation of light at the specified frequency. In all cases, introduction of an endoscope into the body requires some type of sedation or general or local anesthesia. Once a tumor has been located by use of the interventional device, depending upon the type of tumor, photo chemotherapy or other treatment means can be used. However, prior to actual treatment, there must be a confirmed test of cancer. Accordingly, the tumor still needs to be sampled by an appropriate biopsy method. Generally, biopsy methods also require some type of sedation or anesthesia. Thus, traditional methods of confirming a malignancy may require at least two interventional surgical procedures.
- In all uses of photodynamic therapy, it is well known that there are limitations in such therapy because of the poor penetration of the visible light required to activate the administered porophyrin so as to render it toxic to the targeted tissue. Particularly for tumors which are found deep within the body of a patient, repeated interventional procedures to treat the neoplastic tissue become infeasible. Accordingly, many types of diseased tissue cannot be effectively treated through photodynamic therapy.
- Stereotaxic radio surgery is a well known procedure to treat tumorous tissue. This type of radio surgery is particularly well known for treating brain tumors. Advances in technology for delivering a collimated surgical ionizing beam now allows medical personnel to treat patients with cancerous tissue throughout the body.
- One company that provides a stereotaxic radio surgery system is Accuray of Boulder, Colo. One system developed by Accuray includes the Cyberknife™ system that incorporates a linear accelerator mounted on a robotic arm thereby providing a surgeon with great flexibility in delivering a collimated beam to a targeted area. The Cyberknife has been used to radiosurgically treat many tumors and other malformations at body sites which are unreachable by other stereotaxic systems.
- Accuracy is the owner of two U.S. patents which claim devices and methods of carrying out stereotaxic radio surgery and radio therapy. U.S. Pat. No. 5,207,223 discloses a method and apparatus for selectively irradiating a target within a patient. A 3-dimensional mapping is provided of a region surrounding the target. A beaming apparatus emits a collimated beam. Diagnostic beams at a known non-zero angle to one another pass through the mapping region. Images of projections are produced within the mapping region. Electronic representations of the images are compared with reference data from the 3-dimensional mapping thereby locating the target. The relative positions of the beaming apparatus and the living organism are adjusted in such a manner that the collimated beam is focused on the target region despite any movement by the patient during treatment. A comparison is repeated at small time intervals and, when the comparison so indicates, adjustment is repeated, as needed, and in such a manner that the collimated beam remains focused on the target region.
- U.S. Pat. No. 5,427,097 owned by Accuracy discloses another apparatus and method of performing stereotaxic surgery. A robotic arm and beam generating arrangement are provided along a predetermined, non-circular and non-linear path transverse to a collimated beam path, while at the same time, the collimated beam path is directed into the target region. Thus, the radiosurgical/radiotheraputic beam can be directed through the target region from particular treatment points along the transverse path so as to define a non-spherical target region, thereby allowing treatment of irregularly shaped tumors or malformations.
- One important objective of the inventions disclosed in these references owed by Accuracy is to improve the ability to deliver a radiological beam which can be precisely targeted for irradiating targeted tissue, yet limiting exposure of healthy tissue. With the inventions disclosed in the two references, it is possible to perform multiple fraction radiological treatment thereby improving the ability to target and localize cancerous or malformed tissue.
- While the two references discussed immediately above represent advances in stereotaxic radiosurgery and radiotherapy, these systems can be further enhanced by improving the ability to not only map targeted tissue, but also to image the tissue during the radio surgery/radio therapy procedure thereby ensuring that the radiological beam is precisely aligned with the targeted tissue. In the above references, 3-dimensional mapping is obtained by a CAT scan (CT) or by magnetic resonance imaging (MRI). As is well known, computerized tomography operates through measurement of the differential absorption of x-ray beams, and the resulting images are in the form of data which is mathematically manipulated through Fourier transform. MRI utilizes nuclear magnetic resonance properties of tissue to obtain 3-dimensional mapping. CT scanners and MRI scanners are available commercially, and the data obtained by the scanning can be placed in a digitized format whereby it can be stored and manipulated through software in a computer. Although an MRI or CT scan may be adequate under many circumstances, the disadvantages of CT scanning or MRI scanning is that these types of scans image the physical structure of tissue, and do not provide information regarding the body's chemistry, or cell function.
- More recent imaging technologies include positron emission tomography (PET). A PET scan differs from the CT or MRI scan in that the PET scan analyzes cell function, which in many instances provides a better method by which to determine whether tissue is cancerous. PET typically involves the administration of a radioactive form of glucose, and then the PET scanner tracks and records signals which are emitted by the administered compound. Actively growing cancer cells typically have much higher metabolic rates than normal cells; therefore, the radioactive glucose is metabolized more quickly by these cancerous tissues, thereby creating distinct signals which can be recorded by the PET scanner. A computer then reconstructs the recorded signals into 3-dimensional digital images that show areas throughout the body where diseases are present. In addition to PET, a related imaging technology includes single photon emission computer tomography (SPECT) which is also a computerized imaging technique that produces 3-dimensional images of tissue function. As with PET scanning, a small amount of a radioactive isotope is administered to a patient, and any increased metabolic activity present at various body locations can be identified and reviewed to determine whether a patient has diseased or cancerous tissue.
- One class of chemicals useful for the treatment of tumors is the porphyrins and particularly hematoporphyrin derivatives. These chemicals have been studied as a result of their selective localization and uptake into tumors and malignant tissue and their sensitization of tumor tissues to photoirradiation. It has also been suggested that these chemicals could function as delivery vehicles to target other anticancer compounds to tumor tissues due to their selective uptake into tumor tissues. For example, porphyrin molecules may chelate one of many different metal atoms which are then localized to tumor tissues. These metal atoms can be radioactive isotopes which then irradiate the surrounding tumor tissue after localization to the tumor within a metalloporphyrin. Additionally, the radioactivity emitted can be used in PET or SPECT scanning to create an image of the tumor tissue. However, even without a radioactive component, the metalloporphyrins are still effective in selectively delivering a metal atom to tumor tissues. The metal can then act as a contrast agent to enhance magnetic resonance imaging or nuclear magnetic resonance imaging. Because the localization of the metalloporphyrins is based on the chemical properties of the porphyrins themselves and their interaction with characteristics of tumor cells including large interstitial space, high capillary permeability and lack of lymphatic drainage, and not on differences in metabolic activities in tissues, they are more selectively taken up and retained by malignant cells than are radioactive glucose molecules. For this reason, the metalloporphyrins are also better contrast agents for use with the different tumor imaging techniques than are radioactive glucose molecules.
- One reference that discloses the use of metalloporphyrins as imageable tumor targeting agents for radiation therapy is U.S. Pat. No. 6,566,517. This reference specifically discloses halogenated derivatives of boronated porphyrins containing multiple carborane cages which selectively accumulate in neoplastic tissue, and thus can be used in cancer therapies including boron neutron capture therapy and photodynamic therapy. Although this reference generally discusses the uses of metalloporphyrins for radiation therapy, there is no disclosure of particular procedures by which targeted tissue can be mapped, nor is there disclosure of other methods by which cancer screening or treatment therapy can be conducted other than by boron neutron capture or photodynamic therapy.
- The present invention provides a method and apparatus including use of metalloporphyrins for subsequent optimization of radio surgery and radio therapy.
- The present invention may make use of porphyrin compounds complexed with various metals such as silver (Ag), aluminum (Al), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), gadolinium (Gd), indium (In), lutetium (Lu), magnesium (Mg), manganese (Mn), nickel (Ni), palladium (Pd), platinum (Pt), rhodium (Rh), ruthenium (Ru), scandium (Sc), silicon (Si), tin (Sn), titanium oxide (TiO), vanadium oxide (VO), ytterbium (Yb) and zinc (Zn). These complexes are generally categorized as metalloporphyrins meaning a porphyrin moiety having a chelated radioactive isotope of a metal atom. These metalloporphyrins are further processed so that the metal is in the form of a radioactive isotope. The resulting radioactive metalloporphyrins thereby constitute radiopharmaceuticals that can be intravenously introduced to the patient. The affinity of neoplastic tissue for porphyrins results in selective uptake of the radioactive metalloporphyrin, thereby effecting targeted delivery of therapeutic radiopharmaceuticals. For example, in the instance of elemental copper chelated by the porphyrin, the copper can be transformed to radioactive 67Cu. In this way, introduction of the metalloporphyrin radiopharmacuetical to the patient is an effective means to deliver measured radiation therapy to targeted tissue. More specifically, 67Cu provides a source of beta radiation for selective destruction of neoplastic sites. Additionally, metalloporphyrin complexes still provide the ability to simultaneously conduct fluorescence detection and phototherapy if desired. Also, the metalloporphyrins provide the ability for observation of the targeted areas through PET (for example, through the use of 64Cu) or SPECT (for example, through use the of 67Cu).
- A selected group of porphyrin compounds complexed with various metals are specifically contemplated in the present invention because these metalloporphyrins are particularly effective in tumor tissue imaging. The synthetic water soluble porphyrins which contain hydrophilic groups peripheral to the porphyrin ring facilitate oral administration and avoid the use of additional solubilizing agents. Fe (III) and Mn (III) meso-tetra (4-sulfonatophenyl) porphine (TPPS4) are water soluble metalloporphyrins that show an increased affinity for solid tumor cells. This affinity is higher than would be expected for the metalloporphyrins as a general class of compounds. Without intending to be bound by any one theory, it is believed that this increased affinity for solid tumors results from the large size of these metalloporphyrins favoring their retention in the high capacity interstitial space of tumors. Additional factors believed to influence the selective accumulation of the metalloporphyrins in tumors includes charge on the peripheral substituents on the porphyrin ring at physiological pH as well as the plasma binding characteristics of the specific metalloporphyrin. Additionally, Fe (III) and Mn (III) TPPS4 are very stable compounds making them easier to produce, ship and handle either in their non-radioactive form or having radioactive isotopes of iron or manganese atoms. Iron is known to have seven radioisotopes (52Fe, 53Fe, 55Fe, 59Fe, 60Fe, 61Fe, 62Fe) and manganese is known to have six radioisotopes (51Mn, 52Mn, 53Mn, 54Mn, 55Mn, 56Mn, 57Mn) providing many radioisotopes that can be used in the TPPS4 prophyrin molecule. Each of these isotopes can be selected for the desired characteristics in terms of half life and emission spectra that make for the best use in producing, shipping and using the radioisotope in the scanning procedure. For example, 59Fe has a half life about 44.5 days while 62Fe has a half life of about 68 seconds. Similarly, 54Mn has a half life of 312 days whereas 57Mn has a half life of about 1.5 minutes. Thus, the desired radioisotope of these two metal atoms can be selected depending on the photon emission characteristics and a suitable or desired half-life. Table I contains a list of the radioisotopes of these two metal atoms and their half-lives. Therefore, the Fe (III) and Mn (III) derivatives of TPPS4 having a radiometal capable of photo emission are preferred metalloporphyrins for use in the radiosurgery imaging techniques of the present invention.
TABLE I Radioisotope Half-life 52Fe 8.28 hours 53Fe 8.51 minutes 55Fe 2.73 years 59Fe 44.51 days 60Fe 1.5 million years 61Fe 6 minutes 62Fe 68 seconds 51Mn 46.2 minutes 52Mn 5.59 days 53Mn 3.7 million years 54Mn 312.2 days 56Mn 2.58 hours 57Mn 1.45 minutes - In accordance with the present invention, the desired metalloporphyrin may be administered directly to the patient orally, topically, or intravenously. Depending upon the compound introduced, a particular waiting period is necessary for uptake of the porphyrin compound. After sufficient time has been provided for a reaction between the compound and the targeted cells, a cancer screening procedure may take place wherein the patient is subject to an initial PET or SPECT procedure, and either a particular location may be imaged, or the entire body may be imaged, for example, to determine the extent to which a tumor has metastasized. After conducting the initial imaging procedure, 3-dimensional images of targeted body locations are created through mapping and the images are stored in a computer.
- Based upon the results of the initial scanning procedure, subsequent radiosurgery/radiotherapy may take place. In the preferred embodiment, the particular stereotaxic radiosurgery procedure that is contemplated is the same as that disclosed in the above-mentioned U.S. Pat. Nos. 5,207,223 and 5,427,097, these references being incorporated herein by reference in their entireties. The present invention differs from the procedures disclosed in these prior art references by the method in which tissue is imaged. Instead of a CAT scan or MRI scan, 3-dimensional mapping is achieved by PET or SPECT scanning.
- After mapping has been achieved, a beaming apparatus is provided to generate a collimated surgical ionizing beam of a sufficient strength to cause a targeted region to become necrotic. A preferred beaming apparatus includes an x-ray linear accelerator, although other ionizing radiation sources can be used. Means are provided which allow the collimated beam to be precisely aligned with the targeted area through a comparison of imaging data which takes place in real-time during treatment and the previously mapped images. The imaging which takes place during the treatment according to the present invention also includes imaging achieved by PET or SPECT. Assuming the time between creating the mapping images and treatment by use of the ionizing beam extends beyond the effective half-life of the metalloporphyrin, a metalloporphyrin is again administered to the patient prior to the treatment, and the metalloporphyrin metabolized in neoplastic tissue allows a very distinct target by which the collimated beam can be aligned. Images which are obtained real-time during treatment are compared with the previous mapped images, and the collimated beam is adjusted as necessary to maintain the collimated beam in alignment with its targeted location.
- By the use of a metalloporphyrin administered to the patient, additional options are provided in treating cancerous or suspect tissue through radiation therapy/radiosurgical procedures. The metalloporphyrin can be specifically formulated to provide a desired amount of radiation which will not only allow 3-dimensional mapping during a PET/SPECT scanning, but may also provide radiation for treatment by exposure of the suspect tissue during the time in which the metalloporphyrin is metabolized by the tissue. The later radiosurgical procedure by use of an irradiating beam can be dosed to provide the amount of radiation necessary to provide the additional treatment necessary. Accordingly, the initial exposure of the tissue to the metalloporphyrin may result in desired treatment to a specific level, and the remaining required treatment can then be provided by the irradiating beam. Accordingly, the present invention has great flexibility in delivering radiation in two separate ways, namely, the administration of the metalloporphyrin and the use of an irradiating beam. If two administrations of a metalloporphyrin are required (i.e., once for mapping and once for providing real-time images), then the administrations are collectively dosed to deliver the desired amount of radiation.
- One clear advantage to the above method is that in many instances, administration of the metalloporphyrin will greatly shrink a tumor size; therefore, the beam of radiation can be better focused onto a specific targeted area thereby further eliminating exposure of healthy tissue to the irradiating beam.
- Thus, with the present invention, radiosurgery/radiotherapy can be optimized in a manner which enhances the ability to provide a radiosurgical beam to targeted areas in the body and to limit the adverse effects of radiation exposure of healthy tissue.
-
FIG. 1 is a block diagram illustrating the major components enabling completion of the method of the present invention. - In order to execute the method and apparatus of the present invention, a system is provided for delivering a collimated ionizing beam of radiation to a targeted area of tissue. Examples of such systems to support the present invention are disclosed in the U.S. Pat. Nos. 5,427,097 and 5,207,223.
- Referring to
FIG. 1 , a representative system to achieve the present invention includes acomputer 10 with data storage capability that is capable of executing instructions from software loaded within the computer. The computer can store and manipulate 3-dimensionalmapping data images 12 of a patient being treated. The 3-dimensional mapping is typically stored in digital form, and is loaded in thecomputer 10 for later comparison purposes. As mentioned above, the 3-dimensional mapping is preferably achieved by SPECT or PET scanning following administration of a metaloporphyrin to a patient. A beamingapparatus 16 is provided which, when activated, emits a collimated surgical ionizing beam of a sufficient strength to cause a targeted region to become necrotic. Means are provided for generating real-time images 14 of tissue at and around the area which is being treated by the collimated beam during the stereotaxic radiosurgery/radiotherapy. In one form, the real-time images may be created by passing first and second diagnostic beams through the mapping region, the beams being laterally extensive to provide projections of the mapping region such as disclosed in the U.S. Pat. No. 5,207,223. However, the preferred manner in which to provide real-time images for comparison of the previous 3-dimensional mapping is to conduct an additional PET or SPECT procedure. Theseimages 14 in digital form are then loaded into thecomputer 10, and software in the computer then compares the previous 3-dimensional mapping to the real-time images to determine the extent to which the collimated beam must be shifted or adjusted to irradiate the desired tissue. In response to comparison of the real-time images to the previous 3-dimensional mapping, means are provided for adjusting the relative position of the beamingapparatus 16 thereby adjusting the collimated beam to irradiate the desired target. As disclosed in the U.S. Pat. No. 5,427,09, one means to provide adjustment is through a robotic arm which precisely adjusts the collimated beam. - Because images which are taken by the PET or SPECT procedures are of such high quality and very accurately image tissue in three dimensions, the collimated beam can be better controlled, and the strength and duration of the beam can be minimized to provide only the amount of radiation necessary to treat targeted tissue, thereby minimizing exposure of healthy tissue to the radiation.
- If it is desired to perform multiple fraction stereotaxic radiation, such treatment can be provided without having to use fiducials or other markers since the metalloporphyrins will efficiently localize in cancerous tissue, and the images are of such high quality that apparatuses such as a fiducials are therefore unnecessary to provide reference points to help locate suspect areas.
- Radiation therapy can be delivered to a patient in the present method in multiple ways. The initial administration of the metalloporphyrin may have significant therapeutic results, and stereotaxic radiation can then complete the necessary radiation treatment. The dosages of radiation provided both by the metalloporphyrin and the irradiating beam can be selectively adjusted to provide the desired level of treatment. In any case, use of the irradiating beam to treat suspect tissue can be better delivered to the patient because PET/SPECT precisely images suspect tissue. Thus, the irradiating beam can thereby be better aligned and minimized in strength and duration to irradiate only the target region thereby minimizing exposure of healthy tissue that surrounds the suspect tissue.
- While the present invention has been described in connection with a specific preferred embodiment, it shall be understood that various modifications to the present invention can be made within the spirit and the scope of the present invention as defined by the appended claims.
Claims (5)
1-7. (canceled)
8. An apparatus for carrying out radiosurgery by selectively irradiating a targeted area of tissue within a patient, and by providing a selected dose of radiation through administration of an irradiating compound in conjunction with the radiosurgery, comprising:
a computer including data storage memory having stored therein a 3-dimensional mapping of at least a portion of the patient, the mapping covering a mapping region that is larger than a target region;
a beaming apparatus adapted to emit a radiosurgical beam of radiation sufficient to cause the target region to become necrotic;
means for providing digital electronic images of the target region during activation of said radiosurgical beam, said means for providing including PET or SPECT which produces said images based on a metalloporphyrin previously administered to the patient;
means for comparing the 3-dimensional mapping with real-time images taken during activation of said radiosurgical beam; and
means for adjusting the relative position of the beaming apparatus and the patient as needed due to any movement of the target region relative to the radiosurgical beam in response to the comparison of the 3-dimensional mapping and image data taken during activation thereby ensuring that the radiosurgical beam is continuously focused onto the target region.
9. An apparatus as claimed in claim 8 , wherein:
the 3-dimensional mapping is achieved by PET or SPECT scanning.
10. An apparatus as claimed in claim 8 , wherein:
said irradiating compound administered to the patient is meso-tetra (4-sulfonatophenyl) porphine complexed with a radiometal imageable by SPECT or PET imaging selected from the group consisting of manganese and iron.
11. An apparatus for carrying out radiosurgery by selectively irradiating a targeted area of tissue within a patient, and by providing a selected dose of radiation through administration of an irradiating compound in conjunction with the radiosurgery, comprising:
a computer including data storage memory having stored therein a 3-dimensional mapping of at least a portion of the patient, the mapping covering a mapping region that is larger than a target region and achieved by PET or SPECT scanning;
a beaming apparatus adapted to emit a radiosurgical beam of radiation sufficient to cause the target region to become necrotic;
means for providing digital electronic images of the target region during activation of said radiosurgical beam, said means for providing including PET or SPECT which produces said images based on a radio-imageable form of Mn (III) meso-tetra (4-sulfonatophenyl) porphine previously administered to the patient;
means for comparing the 3-dimensional mapping with real-time images taken during activation of said radiosurgical beam; and
means for adjusting the relative position of the beaming apparatus and the patient as needed due to any movement of the target region relative to the radiosurgical beam in response to the comparison of the 3-dimensional mapping and image data taken during activation thereby ensuring that the radiosurgical beam is continuously focused onto the target region.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/532,021 US20070043289A1 (en) | 2002-06-21 | 2006-09-14 | Method and Apparatus Including Use of Metalloporphyrins for Subsequent Optimization of Radiosurgery and Radiotherapy |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/176,558 US6750037B2 (en) | 1999-12-27 | 2002-06-21 | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
US10/836,454 US7110808B2 (en) | 2002-06-21 | 2004-04-30 | Method of optimizing radiosurgery and radiotherapy with metalloporphyrins |
US11/532,021 US20070043289A1 (en) | 2002-06-21 | 2006-09-14 | Method and Apparatus Including Use of Metalloporphyrins for Subsequent Optimization of Radiosurgery and Radiotherapy |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/836,454 Continuation US7110808B2 (en) | 2002-06-21 | 2004-04-30 | Method of optimizing radiosurgery and radiotherapy with metalloporphyrins |
Publications (1)
Publication Number | Publication Date |
---|---|
US20070043289A1 true US20070043289A1 (en) | 2007-02-22 |
Family
ID=29717841
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/176,558 Expired - Fee Related US6750037B2 (en) | 1999-12-27 | 2002-06-21 | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
US10/215,881 Expired - Fee Related US6753160B2 (en) | 2002-06-21 | 2002-08-08 | Method of using metaloporphyrins for treatment of arteriosclerotic lesions |
US10/836,454 Expired - Fee Related US7110808B2 (en) | 2002-06-21 | 2004-04-30 | Method of optimizing radiosurgery and radiotherapy with metalloporphyrins |
US11/532,021 Abandoned US20070043289A1 (en) | 2002-06-21 | 2006-09-14 | Method and Apparatus Including Use of Metalloporphyrins for Subsequent Optimization of Radiosurgery and Radiotherapy |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/176,558 Expired - Fee Related US6750037B2 (en) | 1999-12-27 | 2002-06-21 | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
US10/215,881 Expired - Fee Related US6753160B2 (en) | 2002-06-21 | 2002-08-08 | Method of using metaloporphyrins for treatment of arteriosclerotic lesions |
US10/836,454 Expired - Fee Related US7110808B2 (en) | 2002-06-21 | 2004-04-30 | Method of optimizing radiosurgery and radiotherapy with metalloporphyrins |
Country Status (5)
Country | Link |
---|---|
US (4) | US6750037B2 (en) |
EP (1) | EP1376125B1 (en) |
AT (1) | ATE290690T1 (en) |
CA (1) | CA2432777A1 (en) |
DE (1) | DE60300369D1 (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090256078A1 (en) * | 2008-03-14 | 2009-10-15 | Samuel Mazin | Method and apparatus for emission guided radiation therapy |
CN102697561A (en) * | 2012-05-17 | 2012-10-03 | 深圳市一体医疗科技股份有限公司 | Non-invasive in-vitro tumor positioning system and method by fixing mark points |
US8885034B2 (en) | 1997-10-06 | 2014-11-11 | Micro-Imaging Solutions Llc | Reduced area imaging device incorporated within endoscopic devices |
US9283403B2 (en) | 2011-03-31 | 2016-03-15 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US10500416B2 (en) | 2015-06-10 | 2019-12-10 | Reflexion Medical, Inc. | High bandwidth binary multi-leaf collimator design |
US10603515B2 (en) | 2017-08-09 | 2020-03-31 | Reflexion Medical, Inc. | Systems and methods for fault detection in emission-guided radiotherapy |
US10695586B2 (en) | 2016-11-15 | 2020-06-30 | Reflexion Medical, Inc. | System for emission-guided high-energy photon delivery |
US10702715B2 (en) | 2016-11-15 | 2020-07-07 | Reflexion Medical, Inc. | Radiation therapy patient platform |
US10795037B2 (en) | 2017-07-11 | 2020-10-06 | Reflexion Medical, Inc. | Methods for pet detector afterglow management |
US10918884B2 (en) | 2016-03-09 | 2021-02-16 | Reflexion Medical, Inc. | Fluence map generation methods for radiotherapy |
US11358008B2 (en) | 2018-02-13 | 2022-06-14 | Reflexion Medical, Inc. | Beam station treatment planning and radiation delivery methods |
US11369806B2 (en) | 2017-11-14 | 2022-06-28 | Reflexion Medical, Inc. | Systems and methods for patient monitoring for radiotherapy |
US11406846B2 (en) | 2016-11-15 | 2022-08-09 | Reflexion Medical, Inc. | Methods for radiation delivery in emission-guided radiotherapy |
US11504550B2 (en) | 2017-03-30 | 2022-11-22 | Reflexion Medical, Inc. | Radiation therapy systems and methods with tumor tracking |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6984498B2 (en) * | 1999-12-27 | 2006-01-10 | Adair Edwin L | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
US6750037B2 (en) * | 1999-12-27 | 2004-06-15 | Edwin L. Adair | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
AU2002239269B2 (en) * | 2000-11-17 | 2008-08-21 | Bioaffinity Technologies, Inc. | Compositions and methods for detecting pre-cancerous conditions in cell and tissue samples using 5, 10, 15, 20-tetrakis (carboxyphenyl) porphine |
US20030103995A1 (en) * | 2001-06-04 | 2003-06-05 | Hamblin Michael R. | Detection and therapy of vulnerable plaque with photodynamic compounds |
US6749582B2 (en) * | 2002-04-30 | 2004-06-15 | The First Years Inc. | Pumping breast milk |
DE60307545T2 (en) * | 2002-06-21 | 2007-10-04 | Adair, Edwin L., Castle Pines Village | Use of metalloporphyrins for the treatment of arteriosclerosis |
US20050163821A1 (en) * | 2002-08-02 | 2005-07-28 | Hsing-Wen Sung | Drug-eluting Biodegradable Stent and Delivery Means |
US20040037774A1 (en) * | 2002-08-26 | 2004-02-26 | Chuang - Chun Chiueh | Carrier for carrying radioactive substances and methods for using the same |
AU2003302020B2 (en) * | 2002-11-14 | 2008-01-31 | Ethicon Endo-Surgery, Inc. | Methods and devices for detecting tissue cells |
US7297154B2 (en) * | 2003-02-24 | 2007-11-20 | Maxwell Sensors Inc. | Optical apparatus for detecting and treating vulnerable plaque |
US20040260157A1 (en) * | 2003-06-20 | 2004-12-23 | Montes Miguel A. | Method for automated screening of cervical/endocervical malignant and premalignant epithelial lesions using flow cytometry with HPV DNA fluorescent in-situ hybridization ( FISH) technology |
US8213005B2 (en) | 2003-07-22 | 2012-07-03 | King Saud University | Method for discriminating between benign and malignant prostate tumors |
US7869033B2 (en) * | 2003-12-24 | 2011-01-11 | Vadivel Masilamani | Cancer detection by optical analysis of body fluids |
US8208142B2 (en) * | 2003-12-24 | 2012-06-26 | King Salid University | Lung cancer detection by optical analysis of body fluids |
WO2006085941A1 (en) * | 2004-06-17 | 2006-08-17 | Anazaohealth Corporation | Copper-complex isonitrile positron emission tomography (pet) imaging agent and method |
US7229603B2 (en) * | 2004-06-17 | 2007-06-12 | Anazaohealth Corporation | Stablilized and lyophilized radiopharmaceutical agents |
GB0424294D0 (en) * | 2004-11-03 | 2004-12-01 | Elam T Ltd | Buffer layer |
US7906499B2 (en) * | 2005-01-29 | 2011-03-15 | Children's Hospital & Research Center At Oakland | Polycarboxylated porphyrins and use thereof in treatment of metal toxicities |
WO2006096492A2 (en) * | 2005-03-04 | 2006-09-14 | Dusa Pharmaceuticals, Inc. | Compositions and methods for reducing photosensitivity associated with photodynamic therapy |
US20090041200A1 (en) * | 2005-07-23 | 2009-02-12 | Tomotherapy Incorporated | Radiation therapy imaging and delivery utilizing coordinated motion of jaws, gantry, and couch |
WO2007014090A2 (en) * | 2005-07-23 | 2007-02-01 | Tomotherapy Incorporated | Radiation therapy imaging and delivery utilizing coordinated motion of gantry and couch |
WO2007103427A2 (en) * | 2006-03-06 | 2007-09-13 | Wang Xiang H | Medical use of bilirubin and its structural analogues |
US9339243B2 (en) | 2006-04-14 | 2016-05-17 | William Beaumont Hospital | Image guided radiotherapy with dual source and dual detector arrays tetrahedron beam computed tomography |
EP2026698A4 (en) * | 2006-05-25 | 2016-10-05 | Beaumont Hospital William | Real-time, on-line and offline treatment dose tracking and feedback process for volumetric image guided adaptive radiotherapy |
US8495999B2 (en) | 2007-08-04 | 2013-07-30 | John Adam Law | Airway intubation device |
US20100022824A1 (en) | 2008-07-22 | 2010-01-28 | Cybulski James S | Tissue modification devices and methods of using the same |
US20100121139A1 (en) | 2008-11-12 | 2010-05-13 | Ouyang Xiaolong | Minimally Invasive Imaging Systems |
US8398584B2 (en) | 2009-01-16 | 2013-03-19 | Learning Curve Brands, Inc. | Breast pump and method of use |
EP2414042A4 (en) | 2009-03-31 | 2013-01-30 | Matthew R Witten | System and method for radiation therapy treatment planning using a memetic optimization algorithm |
CN102469928B (en) * | 2009-08-28 | 2014-12-17 | 奥林巴斯医疗株式会社 | Receiver system |
US9179831B2 (en) | 2009-11-30 | 2015-11-10 | King Systems Corporation | Visualization instrument |
EP2521592A4 (en) | 2010-01-05 | 2013-12-18 | Beaumont Hospital William | Intensity modulated arc therapy with continuous couch rotation/shift and simultaneous cone beam imaging |
EP2911743B1 (en) | 2012-10-26 | 2018-08-15 | Brainlab AG | Determining an irradiation region for radiotherapy based on model patient data and patient image data |
CN107469240B (en) | 2013-02-26 | 2020-04-21 | 安科锐公司 | Multi-leaf collimator and system for collimating therapeutic radiation beams |
US11547446B2 (en) | 2014-01-13 | 2023-01-10 | Trice Medical, Inc. | Fully integrated, disposable tissue visualization device |
US9370295B2 (en) | 2014-01-13 | 2016-06-21 | Trice Medical, Inc. | Fully integrated, disposable tissue visualization device |
US10342579B2 (en) | 2014-01-13 | 2019-07-09 | Trice Medical, Inc. | Fully integrated, disposable tissue visualization device |
EP3427796A1 (en) | 2014-09-22 | 2019-01-16 | Koninklijke Philips N.V. | Radiation therapy planning optimization and visualization |
CN113243977A (en) | 2015-08-11 | 2021-08-13 | 特里斯医疗有限公司 | Fully integrated disposable tissue visualization device |
EP3471774A4 (en) | 2016-06-16 | 2020-04-15 | Oncoselect Therapeutics, LLC | Porphyrin compounds and compositions useful for treating cancer |
EP3773235B1 (en) | 2018-03-29 | 2023-07-19 | Trice Medical, Inc. | Fully integrated endoscope with biopsy capabilities |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391547A (en) * | 1990-06-15 | 1995-02-21 | University Of California Office Of Technology Transfer | Method using 5,10,15,20-tetrakis(4-carboxyphenyl)porphine for treating cancers of the lung |
US5427097A (en) * | 1992-12-10 | 1995-06-27 | Accuray, Inc. | Apparatus for and method of carrying out stereotaxic radiosurgery and radiotherapy |
US6920347B2 (en) * | 2000-04-07 | 2005-07-19 | Surgical Navigation Technologies, Inc. | Trajectory storage apparatus and method for surgical navigation systems |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US579262A (en) * | 1897-03-23 | Buttoner | ||
US3394369A (en) | 1965-08-11 | 1968-07-23 | Itt | Display device having light spot projected on screen illuminated by plural colored beams |
US3846490A (en) | 1972-02-24 | 1974-11-05 | N Aronova | Method of producing zeta-aminolevulinic acid hydrochloride |
US3934369A (en) | 1974-04-23 | 1976-01-27 | University Of Illinois Foundation | Vitro net bioxynthesis of chlorophyll and grana |
US3973129A (en) | 1975-01-10 | 1976-08-03 | Bell Telephone Laboratories, Incorporated | Fluorimetric apparatus and method for analysis of body fluid |
US4937187A (en) | 1983-02-04 | 1990-06-26 | Brown University Research Foundation | Methods for separating malignant cells from clinical specimens |
EP0330801A1 (en) | 1983-02-08 | 1989-09-06 | Schering Aktiengesellschaft | Ferromagnetic, diamagnetic or paramagnetic particles useful in the diagnosis and treatment of disease |
US4939240A (en) | 1983-03-04 | 1990-07-03 | Health Research, Inc. | Monoclonal antibodies to human breast carcinoma cells and their use in diagnosis and therapy |
US5122453A (en) | 1984-03-28 | 1992-06-16 | Technicon Instruments Corporation | Method for discriminating surface stained lymphocytes |
US4977177A (en) | 1985-04-30 | 1990-12-11 | Nippon Petrochemicals Company, Ltd. | Tetrapyrrole polyaminomonocarboxylic acid therapeutic agents |
US4897444A (en) | 1985-05-31 | 1990-01-30 | The Research Foundation Of The State University Of New York | Immobilized fluorogenic substrates for enzymes; and processes for their preparation |
US4772691A (en) | 1985-06-05 | 1988-09-20 | The Medical College Of Wisconsin, Inc. | Chemically cleavable nucleotides |
CA1315780C (en) | 1986-01-17 | 1993-04-06 | Yozo Fukuda | Porphyrin derivatives |
US4920143A (en) | 1987-04-23 | 1990-04-24 | University Of British Columbia | Hydro-monobenzoporphyrin wavelength-specific cytotoxic agents |
US5283255A (en) | 1987-01-20 | 1994-02-01 | The University Of British Columbia | Wavelength-specific cytotoxic agents |
US5270171A (en) | 1987-03-06 | 1993-12-14 | Boris Cercek | Cancer-associated SCM-recognition factor, preparation and method of use |
US4886831A (en) | 1987-03-16 | 1989-12-12 | The Regents Of The University Of California | Medical uses for phycocyanin |
US4905670A (en) | 1988-12-28 | 1990-03-06 | Adair Edwin Lloyd | Apparatus for cervical videoscopy |
US5143054A (en) | 1988-12-28 | 1992-09-01 | Adair Edwin Lloyd | Cervical videoscope with detachable camera unit |
US5026368A (en) | 1988-12-28 | 1991-06-25 | Adair Edwin Lloyd | Method for cervical videoscopy |
US5308608A (en) | 1989-06-07 | 1994-05-03 | University Of British Columbia | Photosensitizing Diels-Alder porphyrin derivatives |
US5149708A (en) | 1989-06-07 | 1992-09-22 | University Of British Columbia | Photosensitizing Diels-Alder porphyrin derivatives |
US5422093A (en) | 1989-07-28 | 1995-06-06 | Queen's University | Photochemotherapeutic method using 5-aminolevulinic acid and precursors thereof |
US5955490A (en) | 1989-07-28 | 1999-09-21 | Queen's University At Kingston | Photochemotherapeutic method using 5-aminolevulinic acid and other precursors of endogenous porphyrins |
US5079262A (en) | 1989-07-28 | 1992-01-07 | Queen's University At Kingston | Method of detection and treatment of malignant and non-malignant lesions utilizing 5-aminolevulinic acid |
US5234940A (en) | 1989-07-28 | 1993-08-10 | Queen's University | Photochemotherapeutic method using 5-aminolevulinic acid and precursors thereof |
US4997639A (en) | 1989-11-27 | 1991-03-05 | Nippon Petrochemicals Company, Limited | Method for detecting cholesterol deposited in bodies of mammals |
US5087636A (en) | 1990-02-20 | 1992-02-11 | University Of British Columbia | Method to destroy malignant cells in mononuclear cell populations |
EP0558639A1 (en) | 1990-11-23 | 1993-09-08 | Coulter Corporation | Method and apparatus for optically screening microscopic cells |
US5117465A (en) * | 1991-03-15 | 1992-05-26 | Unex Corporation | Earphone with adjustable headband with progressively shallow detents |
US5117466A (en) | 1991-04-30 | 1992-05-26 | The United States Of America As Represented By The United States Department Of Energy | Integrated fluorescence analysis system |
JP3154742B2 (en) | 1991-04-30 | 2001-04-09 | 日本石油化学株式会社 | Remedy for mammalian atherosclerosis |
US5251613A (en) | 1991-05-06 | 1993-10-12 | Adair Edwin Lloyd | Method of cervical videoscope with detachable camera |
ATE151546T1 (en) | 1991-08-28 | 1997-04-15 | Becton Dickinson Co | GRAVITY ATTRACTION MACHINE FOR ADAPTABLE AUTOCLUSTER FORMATION OF N-DIMENSIONAL DATA STREAMS |
US6096289A (en) | 1992-05-06 | 2000-08-01 | Immunomedics, Inc. | Intraoperative, intravascular, and endoscopic tumor and lesion detection, biopsy and therapy |
EP0663900B1 (en) * | 1992-10-08 | 1999-09-22 | Nycomed Amersham PLC | Metal-oxime chelates for use as radiopharmaceutical agents |
US5981568A (en) | 1993-01-28 | 1999-11-09 | Neorx Corporation | Therapeutic inhibitor of vascular smooth muscle cells |
DE69426948T2 (en) | 1993-02-09 | 2001-10-11 | Becton Dickinson And Co., Franklin Lakes | Automatic determination of the cell line of severe leukaemias by flow cytometry |
US5556764A (en) | 1993-02-17 | 1996-09-17 | Biometric Imaging, Inc. | Method and apparatus for cell counting and cell classification |
EP0618191A1 (en) * | 1993-04-02 | 1994-10-05 | AMERSHAM INTERNATIONAL plc | Metal chelating compounds |
US5441531A (en) | 1993-10-18 | 1995-08-15 | Dusa Pharmaceuticals Inc. | Illuminator and methods for photodynamic therapy |
US5418169A (en) | 1994-03-25 | 1995-05-23 | The Regents Of The University Of California, Office Of Technology Transfer | Chromosome characterization using single fluorescent dye |
US5616114A (en) | 1994-12-08 | 1997-04-01 | Neocardia, Llc. | Intravascular radiotherapy employing a liquid-suspended source |
US5616342A (en) | 1995-04-11 | 1997-04-01 | Pdt, Inc. | Emulsioin suitable for administering a poorly water-soluble photosensitizing compound and use thereof |
US5756726A (en) | 1995-06-02 | 1998-05-26 | Pharmacyclics, Inc. | Methods of producing singlet oxygen using compounds having improved functionalization |
US6008211A (en) | 1995-07-27 | 1999-12-28 | Pdt Pharmaceuticals, Inc. | Photoactivatable compounds comprising benzochlorin and furocoumarin |
US5834503A (en) | 1996-06-14 | 1998-11-10 | Qlt Phototherapeutics, Inc. | Methods to treat arterial plaque |
US6443974B1 (en) | 1996-07-28 | 2002-09-03 | Biosense, Inc. | Electromagnetic cardiac biostimulation |
WO1998048838A1 (en) | 1997-04-29 | 1998-11-05 | Nycomed Imaging As | Compounds |
US6019718A (en) | 1997-05-30 | 2000-02-01 | Scimed Life Systems, Inc. | Apparatus for intravascular radioactive treatment |
US5986693A (en) * | 1997-10-06 | 1999-11-16 | Adair; Edwin L. | Reduced area imaging devices incorporated within surgical instruments |
US6190877B1 (en) * | 1999-12-27 | 2001-02-20 | Edwin L. Adair | Method of cancer screening primarily utilizing non-invasive cell collection and fluorescence detection techniques |
US6750037B2 (en) * | 1999-12-27 | 2004-06-15 | Edwin L. Adair | Method of cancer screening primarily utilizing non-invasive cell collection, fluorescence detection techniques, and radio tracing detection techniques |
EP1401506A4 (en) | 2001-05-31 | 2005-02-16 | Miravant Pharm Inc | Metallotetrapyrrolic photosensitizing agents for use in photodynamic therapy |
US6566517B2 (en) | 2001-06-06 | 2003-05-20 | Brookhaven Science Associates, Llc | Metalloporphyrins and their uses as imageable tumor-targeting agents for radiation therapy |
DE60307545T2 (en) * | 2002-06-21 | 2007-10-04 | Adair, Edwin L., Castle Pines Village | Use of metalloporphyrins for the treatment of arteriosclerosis |
-
2002
- 2002-06-21 US US10/176,558 patent/US6750037B2/en not_active Expired - Fee Related
- 2002-08-08 US US10/215,881 patent/US6753160B2/en not_active Expired - Fee Related
-
2003
- 2003-06-19 AT AT03253897T patent/ATE290690T1/en not_active IP Right Cessation
- 2003-06-19 DE DE60300369T patent/DE60300369D1/en not_active Expired - Lifetime
- 2003-06-19 EP EP03253897A patent/EP1376125B1/en not_active Expired - Lifetime
- 2003-06-19 CA CA002432777A patent/CA2432777A1/en not_active Abandoned
-
2004
- 2004-04-30 US US10/836,454 patent/US7110808B2/en not_active Expired - Fee Related
-
2006
- 2006-09-14 US US11/532,021 patent/US20070043289A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391547A (en) * | 1990-06-15 | 1995-02-21 | University Of California Office Of Technology Transfer | Method using 5,10,15,20-tetrakis(4-carboxyphenyl)porphine for treating cancers of the lung |
US5427097A (en) * | 1992-12-10 | 1995-06-27 | Accuray, Inc. | Apparatus for and method of carrying out stereotaxic radiosurgery and radiotherapy |
US6920347B2 (en) * | 2000-04-07 | 2005-07-19 | Surgical Navigation Technologies, Inc. | Trajectory storage apparatus and method for surgical navigation systems |
Cited By (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8885034B2 (en) | 1997-10-06 | 2014-11-11 | Micro-Imaging Solutions Llc | Reduced area imaging device incorporated within endoscopic devices |
US9667896B2 (en) | 1997-10-06 | 2017-05-30 | Cellect Llc | Reduced area imaging device incorporated within endoscopic devices |
US9307895B2 (en) | 1997-10-06 | 2016-04-12 | Micro-Imaging Solutions, Llc | Reduced area imaging device incorporated within endoscopic devices |
US9198565B2 (en) | 1997-10-06 | 2015-12-01 | Micro-Imaging Solutions | Reduced area imaging device incorporated within endoscopic devices |
US9186052B1 (en) | 1997-10-06 | 2015-11-17 | Micro-Imagaing Solutions | Reduced area imaging device incorporated within endoscopic devices |
US8461538B2 (en) | 2008-03-14 | 2013-06-11 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US8748825B2 (en) | 2008-03-14 | 2014-06-10 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US9820700B2 (en) | 2008-03-14 | 2017-11-21 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US9205281B2 (en) | 2008-03-14 | 2015-12-08 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US11627920B2 (en) | 2008-03-14 | 2023-04-18 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US10959686B2 (en) | 2008-03-14 | 2021-03-30 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US20090256078A1 (en) * | 2008-03-14 | 2009-10-15 | Samuel Mazin | Method and apparatus for emission guided radiation therapy |
US8017915B2 (en) | 2008-03-14 | 2011-09-13 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US10327716B2 (en) | 2008-03-14 | 2019-06-25 | Reflexion Medical, Inc. | Method and apparatus for emission guided radiation therapy |
US9764161B2 (en) | 2011-03-31 | 2017-09-19 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US10617890B2 (en) | 2011-03-31 | 2020-04-14 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US10143857B2 (en) | 2011-03-31 | 2018-12-04 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US10159852B2 (en) | 2011-03-31 | 2018-12-25 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US9694208B2 (en) | 2011-03-31 | 2017-07-04 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US9283403B2 (en) | 2011-03-31 | 2016-03-15 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US10695583B2 (en) | 2011-03-31 | 2020-06-30 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US11141607B2 (en) | 2011-03-31 | 2021-10-12 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
US9649509B2 (en) | 2011-03-31 | 2017-05-16 | Reflexion Medical, Inc. | Systems and methods for use in emission guided radiation therapy |
CN102697561A (en) * | 2012-05-17 | 2012-10-03 | 深圳市一体医疗科技股份有限公司 | Non-invasive in-vitro tumor positioning system and method by fixing mark points |
US11878185B2 (en) | 2015-06-10 | 2024-01-23 | Reflexion Medical, Inc. | High bandwidth binary multi-leaf collimator design |
US10500416B2 (en) | 2015-06-10 | 2019-12-10 | Reflexion Medical, Inc. | High bandwidth binary multi-leaf collimator design |
US11285340B2 (en) | 2015-06-10 | 2022-03-29 | Reflexion Medical, Inc. | High bandwidth binary multi-leaf collimator design |
US10918884B2 (en) | 2016-03-09 | 2021-02-16 | Reflexion Medical, Inc. | Fluence map generation methods for radiotherapy |
US10695586B2 (en) | 2016-11-15 | 2020-06-30 | Reflexion Medical, Inc. | System for emission-guided high-energy photon delivery |
US11794036B2 (en) | 2016-11-15 | 2023-10-24 | Reflexion Medical, Inc. | Radiation therapy patient platform |
US11975220B2 (en) | 2016-11-15 | 2024-05-07 | Reflexion Medical, Inc. | System for emission-guided high-energy photon delivery |
US11406846B2 (en) | 2016-11-15 | 2022-08-09 | Reflexion Medical, Inc. | Methods for radiation delivery in emission-guided radiotherapy |
US10702715B2 (en) | 2016-11-15 | 2020-07-07 | Reflexion Medical, Inc. | Radiation therapy patient platform |
US11504550B2 (en) | 2017-03-30 | 2022-11-22 | Reflexion Medical, Inc. | Radiation therapy systems and methods with tumor tracking |
US11904184B2 (en) | 2017-03-30 | 2024-02-20 | Reflexion Medical, Inc. | Radiation therapy systems and methods with tumor tracking |
US11287540B2 (en) | 2017-07-11 | 2022-03-29 | Reflexion Medical, Inc. | Methods for PET detector afterglow management |
US10795037B2 (en) | 2017-07-11 | 2020-10-06 | Reflexion Medical, Inc. | Methods for pet detector afterglow management |
US12032107B2 (en) | 2017-07-11 | 2024-07-09 | Reflexion Medical, Inc. | Methods for PET detector afterglow management |
US11675097B2 (en) | 2017-07-11 | 2023-06-13 | Reflexion Medical, Inc. | Methods for PET detector afterglow management |
US10603515B2 (en) | 2017-08-09 | 2020-03-31 | Reflexion Medical, Inc. | Systems and methods for fault detection in emission-guided radiotherapy |
US11007384B2 (en) | 2017-08-09 | 2021-05-18 | Reflexion Medical, Inc. | Systems and methods for fault detection in emission-guided radiotherapy |
US11511133B2 (en) | 2017-08-09 | 2022-11-29 | Reflexion Medical, Inc. | Systems and methods for fault detection in emission-guided radiotherapy |
US12023523B2 (en) | 2017-08-09 | 2024-07-02 | Reflexion Medical, Inc. | Systems and methods for fault detection in emission-guided radiotherapy |
US11369806B2 (en) | 2017-11-14 | 2022-06-28 | Reflexion Medical, Inc. | Systems and methods for patient monitoring for radiotherapy |
US12029921B2 (en) | 2017-11-14 | 2024-07-09 | Reflexion Medical, Inc. | Systems and methods for patient monitoring for radiotherapy |
US11801398B2 (en) | 2018-02-13 | 2023-10-31 | Reflexion Medical, Inc. | Beam station treatment planning and radiation delivery methods |
US11358008B2 (en) | 2018-02-13 | 2022-06-14 | Reflexion Medical, Inc. | Beam station treatment planning and radiation delivery methods |
Also Published As
Publication number | Publication date |
---|---|
CA2432777A1 (en) | 2003-12-21 |
US6750037B2 (en) | 2004-06-15 |
US20030235531A1 (en) | 2003-12-25 |
US7110808B2 (en) | 2006-09-19 |
US20020159948A1 (en) | 2002-10-31 |
EP1376125A1 (en) | 2004-01-02 |
EP1376125B1 (en) | 2005-03-09 |
ATE290690T1 (en) | 2005-03-15 |
DE60300369D1 (en) | 2005-04-14 |
US6753160B2 (en) | 2004-06-22 |
US20040202610A1 (en) | 2004-10-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7110808B2 (en) | Method of optimizing radiosurgery and radiotherapy with metalloporphyrins | |
US7394053B2 (en) | Systems and methods for multi-modal imaging having a spatial relationship in three dimensions between first and second image data | |
US6759403B2 (en) | Metalloporphyrins and their uses as radiosensitizers for radiation therapy | |
Lecchi et al. | Current concepts on imaging in radiotherapy | |
US20160256713A1 (en) | Radiation Therapy Guided Using PET Imaging | |
US20150208994A1 (en) | Ct/mri integrated system for the diagnosis of acute strokes and methods thereof | |
EP1404319B1 (en) | Novel metalloporphyrins and their uses as radiosensitizers for radiation therapy | |
RU2004135823A (en) | SENSIBILIZED OPERATIONAL BOLD-MRI IMAGE METHOD | |
US20220273265A1 (en) | Dual modality endocavity biopsy imaging system and method | |
Bugaj | Vascular targeted photochemotherapy using padoporfin and padeliporfin as a method of the focal treatment of localised prostate cancer-clinician’s insight | |
EP3468978B1 (en) | High-affinity compound for targeted boron neutron capture therapy (t-bnct) and use thereof | |
JPH06509117A (en) | Regulatory use of polyether-substituted antitumor agents in diagnosis and therapy | |
US20140142424A1 (en) | Dual modality endocavity biopsy imaging system and method | |
Teng et al. | Cerenkov radiation shining a light for cancer theranostics | |
EP1374912B1 (en) | Use of metaloporphyrins for treatment of arteriosclerotic lesions | |
Zhu et al. | Application of Theranostic Technology in Boron Neutron Capture Therapy | |
Huber et al. | Dual-modality PET/ultrasound imaging of the prostate | |
JP4514907B2 (en) | Diagnosis and treatment equipment | |
RU2788859C2 (en) | Method for targeted brachytherapy of prostate cancer under hybrid psma-receptor scintigraphy navigation | |
KR102441674B1 (en) | An agent for magnetic resonance diagnosis of a neoplastic disease, comprising deuterated 2-amino-2-methylpropionic acid and/or 2-(n-methylamino)-2-methylpropionic acid, and a diagnostic method using the agent | |
Xu | Gold Nanoparticles Enhanced Diffuse Optical Imaging and Radiation Therapy | |
Wong et al. | In vivo assessment of 111In-labeled hematoporphyrin derivative in breast tumor-bearing animals | |
Haberkorn et al. | Radiodiagnostics and Radiotherapy | |
Sause | Technical advances in radiation therapy | |
Adams | Photosensitising Compounds: Their Chemistry, Biology and Clinical use: By TJ Dougherty. Oxford, Wiley, 1989. 241 pp. ISBN 0-471923087.£ 32.50 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |