WO2000040229B1 - Synergistic tumorcidal response induced by histamine - Google Patents

Synergistic tumorcidal response induced by histamine

Info

Publication number
WO2000040229B1
WO2000040229B1 PCT/US2000/000094 US0000094W WO0040229B1 WO 2000040229 B1 WO2000040229 B1 WO 2000040229B1 US 0000094 W US0000094 W US 0000094W WO 0040229 B1 WO0040229 B1 WO 0040229B1
Authority
WO
WIPO (PCT)
Prior art keywords
histamine
administering
cancer therapy
antibody
administration
Prior art date
Application number
PCT/US2000/000094
Other languages
French (fr)
Other versions
WO2000040229A3 (en
WO2000040229A2 (en
Filing date
Publication date
Priority claimed from US09/226,226 external-priority patent/US6498181B1/en
Priority to AU33435/00A priority Critical patent/AU768868B2/en
Priority to KR1020017008517A priority patent/KR20010101379A/en
Priority to JP2000591986A priority patent/JP2002534378A/en
Priority to CA002358754A priority patent/CA2358754A1/en
Priority to IL14377200A priority patent/IL143772A0/en
Application filed filed Critical
Priority to EP00911556A priority patent/EP1140290A2/en
Publication of WO2000040229A2 publication Critical patent/WO2000040229A2/en
Publication of WO2000040229A3 publication Critical patent/WO2000040229A3/en
Publication of WO2000040229B1 publication Critical patent/WO2000040229B1/en
Priority to HK02101636.6A priority patent/HK1040204A1/en
Priority to AU2004201486A priority patent/AU2004201486A1/en

Links

Abstract

The present invention relates to methods of treating cancer in which histamine is administered in conjunction with other cancer therapies. The cancer therapy includes surgery, radiation, immunotherapy, the administration of an agent which enhances the humoral immune response of the patient or any combination thereof.

Claims

AMENDED CLAIMS[received by the International Bureau on 2 January 2001 (02.01.01); original claims 1-29 replaced by amanded claims 1-19; (2 pages)]
1. A method of augmenting a cancer therapy comprising: administering to a subject a pharmaceutically acceptable form of histamine over a period of time such that a blood histamine concentration sufficient to augment the cancer therapy is achieved; and administering to the subject a cancer therapy, wherein the cancer therapy is selected from the group consisting of surgery, radiation, antibody therapy and administration of an agent which enhances the humoral response of the subject.
2. The method of Claim 1, wherein the pharmaceutically acceptable form of histamine is selected from the group consisting of histamine, histamiπe dihydrochloride, histamine phosphate, histamiπe salts, esters, congeners, prodrugs, histamine receptor agonists and diphenyleπeiodonium.
3. The method of Claim 1, wherein the cancer therapy is radiation therapy selected from the group consisting of external beam radiation, radionuciides, radioactive implants, radioactive antibodies, radioactive lipids, radioactive proteins, radioactive giycolipids and radioactive glycoproteins.
4. The method of Claim 1, wherein the cancer therapy is antibody therapy selected from the group consisting of a monoclonal antibody, a humanized monoclonal antibody, an Fab, an (Fab')2, an Fv, an antibody conjugate, an Fab conjugate, an (Fab')2 conjugate, an Fv conjugate and an antibody heteroconjugate.
5. The method of Claim 1, wherein the cancer therapy is administration of an agent which enhances the humoral response of the subject selected from the group consisting of viral antigens, cancer cell antigens, inactivated cancer cells, vaccines and vitamers.
6. The method of Claim 1 further comprising maintaining the stable blood histamine concentration during the administration of the cancer therapy to the subject.
7. The method of Claim 1, wherein the histamine is administered to the subject indirectly by administering a substance which induces the release of endogenous histamine.
8. The method of Claim 7, wherein the substance is selected from the group consisting of retinoic acid, a retinoid, IL-3 or an ingestible allergen.
9. The method of Claim 1, wherein the administration of histamiπe is performed prior to administering the cancer therapy.
10. The method of Claim 1, wherein the administration of histamine is performed after administering the cancer therapy.
11. The method of Claim 1, wherein the administration of histamine is performed during administration of the cancer therapy.
12. The method of Claim 1, wherein the administration of histamine further comprises administering histamine in a dose from 0.1 to 10.0 milligrams per day.
-16-
13. A method of screening cancer treatments comprising: providing a non-human mammal; grafting human tumor cells into the non-human mammal; administering histamine to the non-human mammal; administering a cancer therapy to the non-human mammal, wherein the cancer therapy is selected from the group consisting of administering a radioactive substance, administering an antibody, administering an agent that enhances the humoral immune response of the non-human mammal, radiation, and surgery; and detecting the tumorcidal response of the non-human mammal.
14. The method of Claim 13, wherein the antibody is a monoclonal antibody.
15. The method of Claim 14, wherein the monoclonal antibody is conjugated to a compound selected from the group consisting of a toxin, a radioactive substance, a radionuclide, an antibody fragment or a second antibody.
16. The method of Claim 13, wherein the agent that enhances the humoral immune response of the non-human mammal is a vaccine.
17. The method of Claim 16, wherein the vaccine comprises a killed cancer cell.
18. The method of Claim 13, wherein the radioactive substance comprises a seed implant.
19. The method of Claim 13, wherein the radiation comprises external beam radiation.
-17-
PCT/US2000/000094 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine WO2000040229A2 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
EP00911556A EP1140290A2 (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine
KR1020017008517A KR20010101379A (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine
JP2000591986A JP2002534378A (en) 1999-01-06 2000-01-04 Synergistic tumoricidal response induced by histamine
CA002358754A CA2358754A1 (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine
IL14377200A IL143772A0 (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine
AU33435/00A AU768868B2 (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine
HK02101636.6A HK1040204A1 (en) 1999-01-06 2002-03-04 Synergistic tumorcidal response induced by histamine
AU2004201486A AU2004201486A1 (en) 1999-01-06 2004-04-07 Synergistic tumorcidal response induced by histamine

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/226,226 US6498181B1 (en) 1999-01-06 1999-01-06 Synergistic tumorcidal response induced by histamine
US09/226,226 1999-01-06

Publications (3)

Publication Number Publication Date
WO2000040229A2 WO2000040229A2 (en) 2000-07-13
WO2000040229A3 WO2000040229A3 (en) 2001-07-19
WO2000040229B1 true WO2000040229B1 (en) 2001-08-23

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2000/000094 WO2000040229A2 (en) 1999-01-06 2000-01-04 Synergistic tumorcidal response induced by histamine

Country Status (11)

Country Link
US (3) US6498181B1 (en)
EP (1) EP1140290A2 (en)
JP (1) JP2002534378A (en)
KR (1) KR20010101379A (en)
CN (1) CN1342096A (en)
AU (2) AU768868B2 (en)
CA (1) CA2358754A1 (en)
HK (1) HK1040204A1 (en)
IL (1) IL143772A0 (en)
WO (1) WO2000040229A2 (en)
ZA (1) ZA200104997B (en)

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EP1530474A1 (en) * 2002-07-19 2005-05-18 Ludwig Institute For Cancer Research Enhancing the effect of radioimmunotherapy in the treatment of tumors
BR112013016107A2 (en) * 2010-12-22 2017-04-04 Ifom Fond Inst Firc Di Oncologia Molecolare dimeric molecule, cancer treatment method, pharmaceutical composition and kit for the diagnosis of an upar-mediated pathology or tumor
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