Department of Oncology, The Sixth People's Hospital, Shanghai Jiao Tong University, No. 600 Yishan Road, Shanghai, China.
Breast. 2013 Jun;22(3):314-9. doi: 10.1016/j.breast.2012.07.014. Epub 2012 Aug 14.
To compare doublet agents with single agent as salvage treatment in metastatic breast cancer (MBC) patients pre-treated with an anthracycline and a taxane.
We systematically searched for randomised clinical trials that compared doublet agents with single agent in MBC patients pre-treated with an anthracycline and a taxane. The primary end point was overall survival (OS). Secondary end points were progression-free survival, overall response rate and grade 3 or 4 toxicity. Data were extracted from the studies by two independent reviewers. The meta-analysis was performed by Stata version 10.0 software (Stata Corporation, College Station, TX, USA).
Four trials comprising 2373 patients were eligible for inclusion. Meta-analysis showed that there was significant improvement in progression-free survival (PFS) (hazard ratio (HR) 0.79, 95% confidence interval (CI) 0.72-0.86, P = 0.000) and overall response rate (risk ratio (RR) 1.47, 95%CI 1.13-1.91; p = 0.004) in doublet agents group, though the pooled HR for OS (HR 0.96, 95%CI 0.87-1.05; p = 0.356) showed no significant difference. Subgroup analysis also favoured capecitabine-based doublet agents therapy in terms of PFS (HR 0.77, 95%CI 0.70-0.86; p = 0.000) and overall response rate (ORR) (RR 1.65, 95%CI 1.06-2.56; p = 0.026), but gemcitabine-based doublet agents therapy gained no clinical benefits. There were more incidences of grade 3 or 4 anaemia (RR 1.610, 1.212-2.314, p = 0.01), neutropenia (RR 2.239, 1.231-4.071, p = 0.008), thrombocytopaenia (RR 2.401, 1.595-3.615, p = 0.000), fatigue (RR 2.333, 1.338-4.006, p = 0.000) and nausea and vomiting (RR 2.233, 1.558-3.199, p = 0.000) in the combination group. With regard to the risk of grade 3 or 4 stomatitis (RR 1.666, 0.818-3.392, p = 0.160), diarrhoea (RR 0.739, 0.542-1.008, p = 0.056) and hand-foot syndrome (RR 1.002, 0.835-1.203, p = 0.983), equivalent frequencies were found between the two groups.
Combination chemotherapy offered a significant improvement in PFS and ORR in patients with MBC pre-treated with an anthracycline and a taxane but did not benefit OS. With present available data from randomised clinical trials, we were still unable to clearly set the role of combination therapy in the treatment of MBC in this setting.
比较在接受蒽环类和紫杉类药物预处理的转移性乳腺癌(MBC)患者中,联合用药与单药治疗作为挽救治疗的疗效。
我们系统地检索了比较蒽环类和紫杉类药物预处理的 MBC 患者中联合用药与单药治疗的随机临床试验。主要终点是总生存期(OS)。次要终点是无进展生存期、总缓解率和 3 或 4 级毒性。由两名独立评审员从研究中提取数据。使用 Stata 版本 10.0 软件(Stata 公司,得克萨斯州学院站)进行荟萃分析。
四项试验共纳入 2373 例患者。荟萃分析显示,联合用药组在无进展生存期(PFS)(风险比(HR)0.79,95%置信区间(CI)0.72-0.86,P=0.000)和总缓解率(RR)1.47,95%CI 1.13-1.91;p=0.004)方面有显著改善,但 OS 的合并 HR(HR 0.96,95%CI 0.87-1.05;p=0.356)无显著差异。亚组分析也倾向于卡培他滨联合用药在 PFS(HR 0.77,95%CI 0.70-0.86;p=0.000)和总缓解率(ORR)(RR 1.65,95%CI 1.06-2.56;p=0.026)方面获益,但吉西他滨联合用药未获得临床获益。联合用药组更常见 3 或 4 级贫血(RR 1.610,1.212-2.314,p=0.01)、中性粒细胞减少症(RR 2.239,1.231-4.071,p=0.008)、血小板减少症(RR 2.401,1.595-3.615,p=0.000)、疲劳(RR 2.333,1.338-4.006,p=0.000)和恶心呕吐(RR 2.233,1.558-3.199,p=0.000),而在联合用药组中,3 或 4 级口腔炎(RR 1.666,0.818-3.392,p=0.160)、腹泻(RR 0.739,0.542-1.008,p=0.056)和手足综合征(RR 1.002,0.835-1.203,p=0.983)的风险无差异。
在接受蒽环类和紫杉类药物预处理的 MBC 患者中,联合化疗可显著改善 PFS 和 ORR,但对 OS 无益处。根据目前随机临床试验的可用数据,我们仍然无法明确确定联合治疗在该治疗环境中的作用。