FOLFOX-4 Regimen or Single-agent Gemcitabine as First-line Chemotherapy in Advanced Biliary Tract Cancer

被引:8
|
作者
Novarino, Anna Maria Teresa [1 ]
Satolli, Maria Antonietta [1 ]
Chiappino, Isabella [1 ]
Giacobino, Alice [1 ]
Napoletano, Raffaella [1 ]
Ceccarelli, Manuela [2 ,3 ,4 ]
Ciccone, Gianni [2 ,3 ]
Schena, Marina [1 ]
Bertetto, Oscar [1 ]
Ciuffreda, Libero [1 ]
机构
[1] Univ Turin, Dept Oncol, Turin, Italy
[2] Univ Turin, San Giovanni Battista Hosp, Canc Epidemiol Unit, Turin, Italy
[3] Univ Turin, San Giovanni Battista Hosp, CPO Piemonte, Turin, Italy
[4] Univ Turin, Dept Microbiol & Publ Hlth, Turin, Italy
关键词
5-fluorouracil; biliary tract cancer; gemcitabine; oxaliplatin; PHASE-II TRIAL; GALLBLADDER CARCINOMA; COLORECTAL-CANCER; PLUS OXALIPLATIN; FOLINIC ACID; MITOMYCIN-C; 5-FLUOROURACIL; LEUCOVORIN; CISPLATIN; MULTICENTER;
D O I
10.1097/COC.0b013e31825691c3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives:We conducted a retrospective cohort study to compare 2 different chemotherapy regimens for advanced biliary tract cancer (BTC). Methods:Records of patients consecutively treated in our institution for advanced BTC from 2001 to 2006 were retrieved. Chemotherapy treatment with FOLFOX-4 regimen was routinely offered as first option; gemcitabine (GEM) as single agent was proposed as an alternative option to patients who refused central venous catheter implantation. Toxicity, overall response rate, progression-free survival (PFS), and overall survival (OS) obtained with the 2 treatments were evaluated. Results:Twenty-two patients were treated with FOLFOX-4, whereas 18 patients received GEM. In the FOLFOX-4 group, the overall response rate was 13.6% (95% confidence interval [CI], 4.7-33.3), with 1 complete response and 2 partial responses, and 54.5% (95% CI, 34.7-73.1) of disease control rate (complete response+partial response+stable disease). Median OS was 14.1 months (95% CI, 9.1-18.8) and median PFS 5.44 months (95% CI, 3.2-6.3). In the GEM group, we observed no objective response, whereas 27.7% (95% CI, 12.5-50.9) obtained disease control. Median OS was 8.3 months (95% CI, 4.7-12.9) and median PFS 3.9 months (95% CI, 2.2-5.4). Toxicity, mainly hematological, was acceptable for both treatments. On a multivariable Cox model including a propensity score, only the performance status and chemotherapy regimen were confirmed as strong predictors of OS, with an hazard ratio of 0.49 (95% CI, 0.24-0.99) in favor of FOLFOX-4. Conclusions:The combination chemotherapy with oxaliplatin and 5-fluorouracil is well tolerated and seems to provide prolonged survival than GEM alone in advanced BTC treatment, but further randomized trials are warranted.
引用
收藏
页码:466 / 471
页数:6
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