USE OF CURCUMIN OR ITS ANALOGUES IN CANCER THERAPY UTILIZING EPIDERMAL GROWTH FACTOR RECEPTOR TYROSINE KINASE INHIBITOR

التفاصيل البيبلوغرافية
العنوان: USE OF CURCUMIN OR ITS ANALOGUES IN CANCER THERAPY UTILIZING EPIDERMAL GROWTH FACTOR RECEPTOR TYROSINE KINASE INHIBITOR
Document Number: 20110224205
تاريخ النشر: September 15, 2011
Appl. No: 13/025798
Application Filed: February 11, 2011
مستخلص: Provided is combined use of an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) and curcumin or its analogue in cancer therapy, which reduces side effects resulting from the EGFR-TKI and reduces doses of the EGFR-TKI needed for the therapy, particular in a patient resistant to the treatment with the EGFR-TKI alone.
Inventors: Chen, Huei-Wen (Taipei City, TW); Lee, Jen-Yi (Taichung City, TW); Yang, Pan-Chyr (Taipei City, TW); Yu, Sung-Liang (Taipei City, TW); Chen, Jian-Wei (Taichung City, TW); Yang, Chih-Hsin (Taipei City, TW); Ho, Chao-Chi (Taipei City, TW); Lee, Kuo-Hsiung (Chapel Hill, NC, US); Tseng, Yufeng Jane (Taipei City, TW); Chang, Gee-Chen (Taichung City, TW)
Assignees: NATIONAL TAIWAN UNIVERSITY (TAIPEI CITY, TW)
Claim: 1. A method for reducing side effects resulting from treatment using an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI), comprising administering curcumin or its analogue to a patient undergoing such treatment in an amount effective to reduce the side effects.
Claim: 2. The method of claim 1, wherein the side effects are EGFR-TKI induced adverse gastrointestinal effects.
Claim: 3. The method of claim 2, wherein the side effects are EGFR-TKI induced intestinal cell damage or growth inhibition.
Claim: 4. The pharmaceutical composition of claim 1, wherein the EGFR-TKI is gefitinib (N-(3-Chloro-4-fluoro-phenyl)-7-methoxy-6-(3-morpholin-4-ylpropoxy)quinazolin-4-amine).
Claim: 5. The method of claim 1, wherein the analogue is selected from the group consisting of [chemical expression included]
Claim: 6. The method of claim 1, wherein the patient is afflicted with non-small-cell lung cancer (NSCLC).
Claim: 7. The method of claim 1, wherein the curcumin or its analogue is administered concurrently with the EGFR-TKI.
Claim: 8. A method for administering an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) to a patient in need of a cancer therapy using the EGFR-TKI, comprising administering to the patient a reduced dose of the EGFR-TKI in combination with curcumin or its analogue while efficacy of the EGFR-TKI with respect to the cancer therapy is substantially maintained as compared to that achieved with a standard dose of the EGFR-TKI without administration of the curcumin or its analogue.
Claim: 9. The method of claim 8, wherein the reduced dose is about 50% or less of the standard therapeutic dose of the EGFR-TKI.
Claim: 10. The method of claim 8, wherein the patient is afflicted with NSCLC.
Claim: 11. The method of claim 8, wherein the patient is resistant to treatment with the EGFR-TKI alone.
Claim: 12. The pharmaceutical composition of claim 8, wherein the EGFR-TKI is gefitinib (N-(3-Chloro-4-fluoro-phenyl)-7-methoxy-6-(3-morpholin-4-ylpropoxy)quinazolin-4-amine).
Claim: 13. The method of claim 8, wherein the analogue is selected from the group consisting of: [chemical expression included]
Claim: 14. The method of claim 8, wherein the curcumin or its analogue is administered concurrently with the EGFR-TKI.
Claim: 15. A method for treating a cancer patient with resistance to an EGFR-TKI, which comprises jointly administering to said patient an effective amount of the EGFR-TKI with curcumin or its analogue.
Current U.S. Class: 5142/345
Current International Class: 61; 61; 61
رقم الانضمام: edspap.20110224205
قاعدة البيانات: USPTO Patent Applications