Lowy Cancer Research Centre, Prince of Wales Clinical School, University of New South Wales, Sydney, Australia.
Lowy Cancer Research Centre, Prince of Wales Clinical School, University of New South Wales, Sydney, Australia.
Ann Oncol. 2011 Jun;22(6):1308-1317. doi: 10.1093/annonc/mdq593. Epub 2010 Nov 30.
The addition of HER2-targeted agents to standard treatment has been shown to improve outcomes for HER2 positive metastatic breast cancer patients. We undertook a meta-analysis to evaluate the efficacy of HER2-targeted therapy in addition to standard treatment in metastatic breast cancer patients.
Eligible trials were randomised controlled trials (RCTs) comparing the addition of HER2 therapy to standard treatment (hormone or chemotherapy) reporting overall survival (OS), time to progression (TTP), progression-free survival (PFS) and/or response rates.
Eight trials comprising 1848 patients were eligible for inclusion. HER2-targeted agents were trastuzumab and lapatinib and therapeutic partners were taxanes (4 RCTs), anthracyclines (1), capecitabine (2), anastrozole (1) and letrozole (1). The addition of HER2-targeted agents improved OS [hazard ratios (HR) 0.78; 95% confidence interval (CI) 0.67-0.91], TTP (HR 0.56; 95% CI 0.48-0.64), PFS (HR 0.63; 95% CI 0.53-0.74) and overall response rate (relative risk 1.67; 95% CI 1.46-1.90).
Our meta-analysis confirms the benefit of adding HER2-targeted therapy to standard treatment in HER2 positive metastatic breast cancer. Compared with OS, TTP, PFS and ORR overestimate treatment benefit. Trials in our meta-analysis differed in terms of partner drug or HER2 agents, yet delivered comparable outcomes.
HER2 靶向药物的加入已被证明可以改善 HER2 阳性转移性乳腺癌患者的预后。我们进行了一项荟萃分析,以评估 HER2 靶向治疗在转移性乳腺癌患者标准治疗基础上的疗效。
合格的试验是比较 HER2 治疗联合标准治疗(激素或化疗)与单独标准治疗报告总生存期(OS)、无进展生存期(PFS)和/或反应率的随机对照试验(RCT)。
纳入了 8 项试验,共 1848 例患者。HER2 靶向药物为曲妥珠单抗和拉帕替尼,联合治疗药物为紫杉类(4 项 RCT)、蒽环类(1 项)、卡培他滨(2 项)、阿那曲唑(1 项)和来曲唑(1 项)。HER2 靶向药物的加入改善了 OS[风险比(HR)0.78;95%置信区间(CI)0.67-0.91]、TTP(HR 0.56;95% CI 0.48-0.64)、PFS(HR 0.63;95% CI 0.53-0.74)和总缓解率(相对风险 1.67;95% CI 1.46-1.90)。
我们的荟萃分析证实了在 HER2 阳性转移性乳腺癌中加入 HER2 靶向治疗的益处。与 OS、TTP、PFS 和 ORR 相比,治疗获益被高估了。我们荟萃分析中的试验在联合用药或 HER2 药物方面存在差异,但结果相似。