A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma
- PMID: 15150625
- PMCID: PMC2409742
- DOI: 10.1038/sj.bjc.6601783
A novel biweekly multidrug regimen of gemcitabine, oxaliplatin, 5-fluorouracil (5-FU), and folinic acid (FA) in pretreated patients with advanced colorectal carcinoma
Abstract
Previous results suggest that GEM affects 5-fluorouracil (5-FU) metabolism and pharmacokinetics in cancer patients, while combined with oxaliplatin, levo-folinic acid, and 5-FU (GOLF regimen), at doses achievable in cancer patients, determines high cytotoxic and proapoptotic antitumour activity in colon cancer cells in vitro. On these bases we designed a phase I-II clinical trial testing the GOLF regimen in patients with metastatic colorectal carcinoma, who had received at least a prior line of chemotherapy. In total, 29 patients (20 males and nine females) enrolled in the study received every 2 weeks, gemcitabine (patients #1-3 received 600 mg m(-2); patients # 4-6 received 850 mg m(-2); while patients # 7-29 received 1000 mg m(-2)) on the day 1, levo-folinic acid (100 mg m(-2)) on the days 1 and 2; 5-fluorouracil (400 mg m(-2)) in bolus injection, followed by a 22-h continuous infusion (800 mg m(-2)) on the days 1 and 2, and oxaliplatin (85 mg m(-2)), 6 h after the 5-FU bolus on day 2. The most frequent side effect was grade I-II haematological toxicity. In total, 28 patients were evaluable for response: three achieved a complete response, nine a partial response, 10 had a stable disease, and six progressed. The average time to progression and overall survival of the patients was, respectively, 7.26 and 22 months. Our GOLF combination is well tolerated and seems promising for the treatment of advanced colorectal cancer.
References
-
- Berlin JD, Alberti DB, Arzoomanian RZ, Feierabend CA, Simon KJ, Binger KA, Marnocha RM, Wilding G (1998–99) A phase I study of gemcitabine, 5-fluorouracil and leucovorin in patients with advanced, recurrent, and/or metastatic solid tumors. Invest New Drugs 16(4): 325–330 - PubMed
-
- Cancer TMA (1998) Toxicity of fluorouracil in patients with advanced colorectal cancer: effect of administration schedule and prognostic factors. Meta-Analysis Group in Cancer. J Clin Oncol 16: 3537–3541 - PubMed
-
- Chu E, Mota AC, Fogarasi MC (2001) Antimetabolites. In Cancer Principles and Practice of Oncology, De Vita V, Hellman S, Rosenberg SA (eds). 6th edn, pp 388–415. Philadelphia: Lippincott Williams and Wilkins
-
- Correale P, Cerretani D, Clerici M, Cozzi C, Bruni G, Pozzessere D, Petrioli R, Marsili S, Messinese S, Sabatino M, Giorgi G, Francini G (2000a) Gemcitabine (dFdC), 5-flurouracil (5FU) and folinic acid (FA) in the treatment of patients with gastroenteric carcinomas: a clinical and pharmacological study. Ann Oncol 11(Suppl 2): H20 (abstract)
-
- Correale P, Cerretani D, Marsili S, Pozzessere D, Petrioli R, Messinese S, Sabatino M, Roviello F, Pinto E, Francini G, Giorgi G (2003) Gemcitabine increases 5-fluorouracil systemic exposure in advanced cancer patients: pharmacokinetic considerations. Eur J Cancer 39(11): 1547–1551 - PubMed
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