Two-Week Combination Chemotherapy with Gemcitabine, High-Dose Folinic Acid and 5 Fluorouracil (GEMFUFOL) as First-Line Treatment of Metastatic Biliary Tract Cancers


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Unal O. U., ÖZTOP İ., ÜNEK İ. T., Yilmaz A. U.

ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, cilt.14, sa.9, ss.5263-5267, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 14 Sayı: 9
  • Basım Tarihi: 2013
  • Doi Numarası: 10.7314/apjcp.2013.14.9.5263
  • Dergi Adı: ASIAN PACIFIC JOURNAL OF CANCER PREVENTION
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.5263-5267
  • Anahtar Kelimeler: Metastatic biliary tract cancer, gemcitabine, 5-fluorouracil, high-dose folinic acid, PHASE-II TRIAL, CISPLATIN PLUS GEMCITABINE, INFUSIONAL 5-FLUOROURACIL, PROGNOSTIC-FACTORS, BILE-DUCT, CARCINOMA, MULTICENTER, GALLBLADDER, LEUCOVORIN, CAPECITABINE
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Background: The aim of this study was to evaluate the efficacy and tolerability of a gemcitabine, 5-fluorouracil and leucovorin (GEMFUFOL) chemotherapy regimen as first line treatment of metastatic biliary tract cancer. Materials and Methods: All patients received folinic acid 400 mg/m(2) on day 1, 5-fluorouracil bolus 400 mg/m(2) on day 1, IV infusion of 5-fluorouracil 2400 mg/m(2) over 46 hours, and gemcitabine 1250 mg/m(2) on day 1. Results: A total of 29 patients with metastatic biliary tract cancer received GEMFUFOL regimen as the first-line treatment. The mean follow-up was 22.1 months (95% CI, 12.5-31.8). One patient (3.4%) achieved complete response, 5 (17.2%) had partial response, and 4 (13.8%) had stable disease. The median progression-free survival was 3.3 months (95% CI, 2.9-3.7), and the median overall survival was 8.8 months (95% CI, 3.5-14). The 1-year and 2-year survival rates were 58.6% and 30%, respectively. Grade 3 and 4 toxicity included neutropenia in 4 patients (13.7%), thrombocytopenia in 2 (6.8%), anemia in 2 (6.8%), and alopecia in 1 (3.4%). Two patients (6.8%) developed febrile neutropenia. A dose reduction was achieved in 8 patients (27.6%) while 5 patients had extended-interval dosage (17.2%) for toxicity. Conclusions: The GEMFUFOL chemotherapy regimen was generally efficacious and tolerable as a first-line treatment of metastatic biliary tract cancer.