Gemcitabine-based combinations for inoperable pancreatic cancer:: Have we made real progress?: A meta-analysis of 20 phase 3 trials

被引:72
作者
Bria, Emilio
Milella, Michele
Gelibter, Alain
Cuppone, Federica
Pino, Maria Simona
Ruggeri, Enzo Maria
Carlini, Paolo
Nistico, Cecilia
Terzoli, Edmondo
Cognetti, Francesco
Giannarelli, Diana
机构
[1] Regina Elena Inst Canc Res, Dept Med Oncol, I-00144 Rome, Italy
[2] Regina Elena Inst Canc Res, Dept Biostat, I-00144 Rome, Italy
关键词
pancreatic cancer; meta-analysis; gemcitabine; combinations; survival;
D O I
10.1002/cncr.22809
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Several attempts have been made at improving the efficacy of gemcitabine in advanced pancreatic cancer by combining it with other chemotherapeutic or molecularly targeted agents. However, randomized trials have produced conflicting results. Methods. All prospective, randomized, phase 3 trials that compared single-agent gemcitabine with gemcitabine-based combinations were considered eligible for the current analysis. A literature- based meta-analysis was performed, event-based relative risk ratios with 95% confidence intervals were derived through both a fixed-effect model approach and a random-effect model approach, and overall survival (OS) was explored as the primary endpoint. To estimate the magnitude of the eventual benefit, absolute differences and the number of patients needed to treat (NNT) for 1 patient to benefit were calculated. A sensitivity analysis for OS was performed according to the type of agent used in combination with gemcitabine. Results. Twenty trials that involved 6296 patients were identified. No significant differences in the primary endpoint were observed in the overall population or in the sensitivity analysis. Conversely, a significant advantage was evident with regard to both progression- free survival (PFS) and the overall response rate (ORR) in the overall population, with an absolute benefit of 2.6% (NTT 39 patients) and 3.0% (NNT = 33 patients). Platinum combinations led to the greatest absolute benefits for PFS and ORR compared with single-agent gemcitabine (10% and 6.5%, respectively), but this did not result in an OS benefit. Improvement in PFS, but not in the ORR, was correlated with an improvement in OS. Conclusions. Single-agent gemcitabine remains the standard of care for patients with advanced pancreatic cancer. However, platinum/ gemcitabine combinations appeared to improve PFS and the ORR and, thus, may be considered in selected patients.
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收藏
页码:525 / 533
页数:9
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