DK2552415T3 - Fremgangsmåder til behandling af cancer - Google Patents
Fremgangsmåder til behandling af cancer Download PDFInfo
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- DK2552415T3 DK2552415T3 DK11763292.7T DK11763292T DK2552415T3 DK 2552415 T3 DK2552415 T3 DK 2552415T3 DK 11763292 T DK11763292 T DK 11763292T DK 2552415 T3 DK2552415 T3 DK 2552415T3
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- paclitaxel
- nsclc
- albumin
- platinum
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
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- A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
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- A61K33/243—Platinum; Compounds thereof
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- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/38—Albumins
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- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
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- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5052—Proteins, e.g. albumin
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
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- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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Claims (15)
1. Sammensætning omfattende nanopartikler omfattende paclitaxel og en albumin til anvendelse i en fremgangsmåde til behandling af NSCLC hos et individ, hvor NSCLC er pladeepithelcarcinom, hvor fremgangsmåden endvidere omfatter at indgive et platin-baseret middel til individet.
2. Sammensætning til anvendelse ifølge krav 1, hvor fremgangsmåden endvidere omfatter at udvælge individet til behandling baseret på karakteristika valgt fra gruppen bestående af (i) differentierede niveauer af caveolin-1 (CAV1), (ii) differentierede niveauer af SPARC, (iii) differentierede niveauer af hypoksimarkører, (iv) differentierede niveauer af tumoraciditet, (v) differentierede niveauer af gp60, (vi) differentierede niveauer af thymidylat syntase (TS), (vii) differentierede niveauer af S-fase kinase-associeret protein (Skp2), (viii) differentieret tab af heterozygositet (LOH) af enkel-nukleotid polymorfi (SNP), (ix) differentierede Kras-mutationer, (x) differentieret metylering af promotorregion af tumor-relaterede gener, og (xi) differentieret albuminoptagelse.
3. Sammensætning til anvendelse ifølge krav 2, hvor differentierede niveau af hypoksimarkører er et differentieret niveau af carboanhydrase-9 (CA-9) eller et differentieret niveau af LDH, fortrinsvis LDH-5; eller hvor det differentierede niveau af tumoraciditet er baseret på et differentieret niveau af HIF-1 a, et differentieret niveau af HIF-2a, eller et differentieret niveau af differentieret embryo-chondrocyt-udtrykt gen 1 (DEC-1).
4. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-3, hvor fremgangsmåden omfatter at indgive sammensætningen omfattende nanopartikler omfattende paclitaxel og albumin i en mængde på mellem ca. 50 mg/m2 og ca. 125 mg/m2.
5. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-4, hvor fremgangsmåden omfatter: indgivelse af sammensætningen omfattende nanopartikler omfattende paclitaxel og albumin en gang om ugen; eller indgivelse af det platin-baserede middel i en mængde på mellem ca. AUC=2 og ca. AUC=6; eller indgivelse af det platin-baserede middel en gang hver tredje uge.
6. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-5, hvor fremgangsmåden omfatter indgivelse af sammensætningen omfattende nanopartikler omfattende paclitaxel og albumin i en mængde på 100 mg/m2 en gang om ugen og det platin-baserede middel i en mængde på AUC=6 en gang hver tredje uge.
7. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-6, hvor paclitaxel i nanopartiklerne er belagt med albumin; eller hvor nanopartiklerne i sammensætningen har en gennemsnitsdiameter på ikke mere end ca. 200 nm.
8. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-7, hvor NSCLC er Stadie IIIB NSCLC eller Stadie IV NSCLC.
9. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-8, hvor sammensætningen omfattende nanopartikler omfattende paclitaxel og albumin og det platin-baserede middel indgives parenteralt, fortrinsvis intravenøst.
10. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-9, hvor det platin-baserede middel er carboplatin.
11. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-10, hvor individet er et menneske.
12. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 1-11, hvor fremgangsmåden endvidere omfatter administrering af thorakal stråling.
13. Sammensætning til anvendelse ifølge krav 12 for så vidt som den afhænger af kravene 1-3, 5 og 7-11, hvor fremgangsmåden omfatter indgivelse af sammensætningen omfattende nanopartikler omfattende paclitaxel og albumin i en mængde på mellem ca. 20 mg/m2 til ca. 60 mg/m2 en gang om ugen, et platinbaseret middel i en mængde på mellem ca. AUC=2 til ca. AUC=6 en gang om ugen, og den thorakale stråling i en mængde på mellem ca. 25 til ca. 40 fraktioner ved enten 3D konform eller intensitets-modulerede teknikker samtidigt.
14. In vitro fremgangsmåde til at vurdere hvorvidt et individ med NSCLC vil reagere på behandling, hvor fremgangsmåden omfatter at vurdere et eller flere karakteristika af NSCLC valgt fra gruppen bestående af (a) pladeepithelcarcinom, (b) differentierede niveauer af caveolin-1 (CAV1), (c) differentierede niveauer af SPARC, (d) differentierede niveauer af hypoksimarkører, (e) differentierede niveauer af tumoraciditet, (f) differentierede niveauer af gp60, (g) differentierede niveauer af thymidylat syntase (TS), (h) differentierede niveauer af S-fase kinase-associeret protein (Skp2), (i) differentieret tab af heterozygositet (LOH) af enkel-nukleotid polymorfi (SNP), (j) differentierede Kras-mutationer, (k) differentieret metylering af promotorregion af tumor-relaterede gener, og (1) differentieret albuminoptagelse, hvor et eller flere karakteristika af NSCLC indikerer at individet vil være modtagelig overfor behandlingen og hvor behandlingen omfatter i) en sammensætning omfattende nanopartikler omfattende paclitaxel og en albumin og ii) et platin-baseret middel.
15. In vitro fremgangsmåde til at identificere et individ med NSCLC som sandsynligvis vil være modtagelig overfor behandling, hvor behandlingen omfatter a) en sammensætning omfattende nanopartikler omfattende paclitaxel og en albumin og b) et platin-baseret middel, hvor fremgangsmåden omfatter: (A) at vurdere et eller flere karakteristika af NSCLC valgt fra gruppen bestående af (i) pladeepithelcarcinom, (ii) differentierede niveauer af caveolin-1 (CAV1), (iii) differentierede niveauer af SPARC, (iv) differentierede niveauer af hypoksimarkører, (v) differentierede niveauer af tumoraciditet, (vi) differentierede niveauer af gp60, (vii) differentierede niveauer af thymidylat syntase (TS), (viii) differentierede niveauer af S-fase kinase-forbundet protein (Skp2), (ix) differentieret tab af heterozygositet (LOH) af enkel-nukleotid polymorf (SNP), (x) differentierede Kras-mutationer, (xi) differentieret metylering af promotorregion af tumorrelaterede gener, og (xii) differentieret albuminoptagelse; og (B) at identificere individet med et eller flere karakteristika af NSCLC valgt fra gruppen bestående af (i) pladeepithelcarcinom, (ii) differentierede niveauer af caveolin-1 (CAV1), (iii) differentierede niveauer af SPARC, (iv) differentierede niveauer af hypoksimarkører, (v) differentierede niveauer af tumoraciditet, (vi) differentierede niveauer af gp60, (vii) differentierede niveauer af thymidylat syntase (TS), (viii) differentierede niveauer af S-fase kinase-forbundet protein (Skp2), (ix) differentieret tab af heterozygositet (LOH) af enkel-nukleotid polymorf (SNP), (x) differentierede Kras-mutationer, (xi) differentieret metylering af promotorregion af tumorrelaterede gener, og (xii) differentieret albuminoptagelse.
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Application Number | Priority Date | Filing Date | Title |
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US31877410P | 2010-03-29 | 2010-03-29 | |
US201161433132P | 2011-01-14 | 2011-01-14 | |
PCT/US2011/030209 WO2011123395A1 (en) | 2010-03-29 | 2011-03-28 | Methods of treating cancer |
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DK2552415T3 true DK2552415T3 (da) | 2016-11-28 |
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Application Number | Title | Priority Date | Filing Date |
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DK11763292.7T DK2552415T3 (da) | 2010-03-29 | 2011-03-28 | Fremgangsmåder til behandling af cancer |
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US (4) | US9393318B2 (da) |
EP (2) | EP3141245A1 (da) |
JP (5) | JP5926724B2 (da) |
KR (2) | KR20130028728A (da) |
CN (1) | CN103118665B (da) |
AU (1) | AU2016202000B2 (da) |
BR (1) | BR112012024442A2 (da) |
CA (2) | CA3087813A1 (da) |
CR (1) | CR20120528A (da) |
CY (1) | CY1118216T1 (da) |
DK (1) | DK2552415T3 (da) |
ES (1) | ES2600912T3 (da) |
HU (1) | HUE030207T2 (da) |
IL (1) | IL276362A (da) |
LT (1) | LT2552415T (da) |
MX (1) | MX364637B (da) |
NZ (3) | NZ717490A (da) |
PL (1) | PL2552415T3 (da) |
PT (1) | PT2552415T (da) |
RU (2) | RU2589513C2 (da) |
SG (2) | SG184160A1 (da) |
SI (1) | SI2552415T1 (da) |
TW (4) | TWI600427B (da) |
WO (1) | WO2011123395A1 (da) |
Families Citing this family (38)
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US8853260B2 (en) | 1997-06-27 | 2014-10-07 | Abraxis Bioscience, Llc | Formulations of pharmacological agents, methods for the preparation thereof and methods for the use thereof |
CN104587479A (zh) | 2002-12-09 | 2015-05-06 | 阿布拉西斯生物科学有限责任公司 | 组合物和传递药剂的方法 |
US8735394B2 (en) | 2005-02-18 | 2014-05-27 | Abraxis Bioscience, Llc | Combinations and modes of administration of therapeutic agents and combination therapy |
PT1853250E (pt) | 2005-02-18 | 2012-02-03 | Abraxis Bioscience Llc | Combinações e modos de administração de agentes terapêuticos e terapia de combinação |
CN103054798B (zh) * | 2005-08-31 | 2021-03-16 | 阿布拉科斯生物科学有限公司 | 用于制备稳定性增加的水难溶性药物的组合物和方法 |
AU2007334360B2 (en) | 2006-12-14 | 2013-10-17 | Abraxis Bioscience, Llc | Breast cancer therapy based on hormone receptor status with nanoparticles comprising taxane |
HUE039643T2 (hu) * | 2007-03-07 | 2019-01-28 | Abraxis Bioscience Llc | Rapamicin rákellenes szert és albumint tartalmazó nanorészecske |
EP2155188B1 (en) * | 2007-06-01 | 2013-10-09 | Abraxis BioScience, LLC | Methods and compositions for treating recurrent cancer |
WO2010121000A1 (en) | 2009-04-15 | 2010-10-21 | Abraxis Bioscience, Llc | Prion-free nanoparticle compositions and methods |
PL2552438T3 (pl) | 2010-03-26 | 2016-12-30 | Sposoby leczenia raka wątrobowokomórkowego | |
CA2794147A1 (en) | 2010-03-29 | 2011-10-06 | Abraxis Bioscience, Llc | Use of a composition comprising nanoparticles comprising a taxane and an albumin to improve uptake of chemotherapeutics by tumors and for treating a cancer that is highly fibrotic and/or has a dense stroma |
MX364637B (es) | 2010-03-29 | 2019-05-03 | Abraxis Bioscience Llc Star | Platino y nanopartículas que incluyen placlitaxel/albúmina para usarse en el trartamiento de nsclc. |
KR20190130050A (ko) | 2010-06-04 | 2019-11-20 | 아브락시스 바이오사이언스, 엘엘씨 | 췌장암의 치료 방법 |
RU2016103126A (ru) * | 2010-06-07 | 2018-11-22 | АБРАКСИС БАЙОСАЙЕНС, ЭлЭлСи | Способы комбинированной терапии для лечения пролиферативных заболеваний |
WO2012129371A2 (en) * | 2011-03-22 | 2012-09-27 | Nant Holdings Ip, Llc | Reasoning engines |
KR20200051841A (ko) | 2011-04-28 | 2020-05-13 | 아브락시스 바이오사이언스, 엘엘씨 | 나노입자 조성물의 혈관내 전달 및 그의 용도 |
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