Manchester Academic Health Sciences Centre, The Christie NHS Foundation Trust, Manchester, UK.
Ann Oncol. 2014 Feb;25(2):391-8. doi: 10.1093/annonc/mdt540. Epub 2013 Dec 18.
Two recent studies (ABC-02 [UK] and BT22 [Japan]) have demonstrated the superiority of cisplatin and gemcitabine (CisGem) chemotherapy over gemcitabine (Gem) alone for patients with pathologically proven advanced biliary tract cancer (BTC: cholangiocarcinoma, gallbladder and ampullary cancers). This pre-planned analysis evaluates the efficacy of CisGem with increased statistical power.
We carried out a meta-analysis of individual patient-level data of these studies to establish the effect of CisGem versus Gem on progression-free survival (PFS), overall survival (OS) and carried out exploratory subgroup analyses.
CisGem demonstrates a significant improvement in PFS [hazard ratio (HR)=0.64, 95% confidence interval (CI) 0.53-0.76, P<0.001] and OS (HR=0.65, 95% CI 0.54-0.78, P<0.001) over Gem. This effect is most marked among patients with good performance status (PS 0-1): HR for PFS is 0.61 (95% CI 0.51-0.74), P<0.001 and OS HR=0.64 (95% CI 0.53-0.77), P<0.001. CisGem resulted in improved PFS and OS for intra- and extra-hepatic cholangiocarcinomas and gallbladder cancer. The treatment effect between UK and Japanese patients was consistent with respect to OS (HR=0.65, 95% CI 0.53-0.79 and 0.65, 95% CI 0.42-1.03, respectively); with similar OS in the combination arms (median 11.7 and 11.1 months, respectively). Subgroups least likely to benefit included patients with ampullary tumours and poor performance status (PS2).
CisGem is the standard of care for the first-line treatment of good-PS patients with advanced BTC regardless of ethnicity. Future studies should aim to enhance the effectiveness of this regimen in the first-line setting, establish the role of subsequent (second-line) therapy and assess the role of rationally developed molecular-targeted therapies.
两项最近的研究(ABC-02[英国]和 BT22[日本])表明,对于病理证实的晚期胆道癌(BTC:胆管癌、胆囊和壶腹癌)患者,顺铂和吉西他滨(CisGem)化疗优于吉西他滨(Gem)单药治疗。本预先计划的分析使用增加的统计效力评估 CisGem 的疗效。
我们对这些研究的个体患者水平数据进行了荟萃分析,以确定 CisGem 与 Gem 在无进展生存期(PFS)、总生存期(OS)上的疗效,并进行了探索性亚组分析。
CisGem 显著改善了 PFS[风险比(HR)=0.64,95%置信区间(CI)0.53-0.76,P<0.001]和 OS(HR=0.65,95%CI 0.54-0.78,P<0.001)与 Gem 相比。这种效果在表现状态(PS 0-1)良好的患者中最为明显:PFS 的 HR 为 0.61(95%CI 0.51-0.74),P<0.001,OS 的 HR=0.64(95%CI 0.53-0.77),P<0.001。CisGem 改善了肝内和肝外胆管癌以及胆囊癌患者的 PFS 和 OS。英国和日本患者的治疗效果在 OS 方面一致(HR=0.65,95%CI 0.53-0.79 和 0.65,95%CI 0.42-1.03);联合治疗组的 OS 相似(中位数分别为 11.7 和 11.1 个月)。不太可能受益的亚组包括壶腹肿瘤和表现状态差(PS2)的患者。
CisGem 是表现状态良好的晚期 BTC 患者一线治疗的标准治疗方法,无论种族如何。未来的研究应旨在提高该方案在一线治疗中的有效性,确定后续(二线)治疗的作用,并评估合理开发的分子靶向治疗的作用。