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Merck

FOLFIRINOX bevacizumab is a promising therapy for chemorefractory metastatic colorectal cancer.

Oncology (2014-07-12)
Marie Chaix, Julie Vincent, Véronique Lorgis, François Ghiringhelli
RESUMEN

Fluoropyrimidines, oxaliplatin, irinotecan and targeted therapies represent the standard treatment of metastatic colorectal cancer. After failure of all these treatments, few options are available. In such chemorefractory patients the effect of triplet chemotherapy with bevacizumab (FOLFIRINOX bevacizumab) has never been investigated. 49 consecutive patients bearing unresectable metastatic colorectal cancer and who experienced failure to oxaliplatin- and irinotecan-based chemotherapy were treated with oxaliplatin (85 mg/m(2)), irinotecan (180 mg/m(2)), leucovorin (400 mg/m(2)), and fluorouracil (400 mg/m(2) bolus then 2,400 mg/m(2)) repeated every 2 weeks. Median age was 63 (range 36-82) years. After a median follow-up of 12 months, the median progression-free survival was 5.8 months (95% CI 3.4-6.8) and the median overall survival was 11.9 months (95% CI 8-18). The response rate after the cycle was evaluable for 36 patients, whereby we observed 18% (95% CI 8-35) partial or complete response, 45% (95% CI 28-68) stable disease of more than 2 months, and 37% (95% CI 21-58) progression. This study suggests that bevacizumab + FOLFIRINOX may be active in mCRC patients after failure of classical lines of chemotherapy.

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5-Fluorouracil, ≥99% (HPLC), powder
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Oxaliplatin, powder
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Folinic acid calcium salt hydrate, BioXtra, ≥99.0% (HPLC)
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Folinic acid calcium salt hydrate, analytical standard
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Irinotecan hydrochloride, topoisomerase inhibitor
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Calcium folinate, European Pharmacopoeia (EP) Reference Standard
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5-Fluorouracil, analytical standard
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Fluorouracil, European Pharmacopoeia (EP) Reference Standard
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