Sultana Asma, Smith Catrin Tudur, Cunningham David, Starling Naureen, Neoptolemos John P, Ghaneh Paula
Cancer Research UK Liverpool Cancer Trials Unit and Centre for Medical Statistics and Health Evaluation, University of Liverpool, Liverpool, United Kingdom.
J Clin Oncol. 2007 Jun 20;25(18):2607-15. doi: 10.1200/JCO.2006.09.2551.
There are a large number of randomized controlled trials involving chemotherapy in the management of advanced pancreatic cancer. Several chemotherapeutic agents, either alone or in combination with other chemotherapy or novel agents, have been used. The aim of these meta-analyses was to examine the different therapeutic approaches, and the comparisons examined were as follows: chemotherapy versus best supportive care; fluorouracil (FU) versus FU combination chemotherapy; gemcitabine versus FU; and gemcitabine versus gemcitabine combination chemotherapy.
Relevant trials were identified by searching databases, trial registers, and conference proceedings. The primary end point was overall survival.
One hundred thirteen randomized controlled trials were identified, of which 51 trials involving 9,970 patients met the inclusion criteria. Chemotherapy improved survival compared with best supportive care (hazard ratio [HR] = 0.64; 95% CI, 0.42 to 0.98). FU-based combination chemotherapy did not result in better overall survival compared with FU alone (HR = 0.94; 95% CI, 0.82 to 1.08). There was insufficient evidence of a survival difference between gemcitabine and FU, but the wide CI includes clinically important differences in both directions, making a clear conclusion difficult (HR = 0.75; 95% CI, 0.42 to 1.31). Survival was improved after gemcitabine combination chemotherapy compared with gemcitabine alone (HR = 0.91; 95% CI, 0.85 to 0.97).
There was a significant survival benefit for chemotherapy over best supportive care and gemcitabine combinations over gemcitabine alone. This supports the use of gemcitabine-based combination chemotherapy in the treatment of advanced pancreatic cancer.
有大量关于晚期胰腺癌治疗中化疗的随机对照试验。已经使用了几种化疗药物,单独使用或与其他化疗药物或新型药物联合使用。这些荟萃分析的目的是研究不同的治疗方法,所进行的比较如下:化疗与最佳支持治疗;氟尿嘧啶(FU)与FU联合化疗;吉西他滨与FU;以及吉西他滨与吉西他滨联合化疗。
通过检索数据库、试验注册库和会议论文集来确定相关试验。主要终点是总生存期。
共识别出113项随机对照试验,其中51项试验涉及9970例患者符合纳入标准。与最佳支持治疗相比,化疗可改善生存期(风险比[HR]=0.64;95%可信区间[CI],0.42至0.98)。与单独使用FU相比,基于FU的联合化疗并未带来更好的总生存期(HR=0.94;95%CI,0.82至1.08)。吉西他滨与FU之间生存期存在差异的证据不足,但较宽的CI包含了两个方向上具有临床意义的差异,难以得出明确结论(HR=0.75;95%CI,0.42至1.31)。与单独使用吉西他滨相比,吉西他滨联合化疗后生存期得到改善(HR=0.91;95%CI,0.85至0.97)。
化疗相对于最佳支持治疗以及吉西他滨联合用药相对于单独使用吉西他滨均有显著的生存获益。这支持在晚期胰腺癌治疗中使用基于吉西他滨的联合化疗。