Gennari Alessandra, Sormani Maria Pia, Pronzato Paolo, Puntoni Matteo, Colozza Mariantonietta, Pfeffer Ulrich, Bruzzi Paolo
National Cancer Research Institute, Largo Rosanna Benzi, 10 16132 Genoa, Italy.
J Natl Cancer Inst. 2008 Jan 2;100(1):14-20. doi: 10.1093/jnci/djm252. Epub 2007 Dec 25.
Adjuvant chemotherapy with anthracyclines improves disease-free and overall survival compared with non-anthracycline-based adjuvant chemotherapy regimens in the treatment of early breast cancer. The role of HER2 status as a marker of anthracycline responsiveness has been explored by subset analyses within randomized clinical trials, with inconsistent results. We performed a pooled analysis of the interaction between HER2 status and the efficacy of adjuvant anthracyclines based on the published subset data.
We searched literature databases to identify randomized trials that compared anthracycline-based with non-anthracycline-based adjuvant chemotherapy regimens in the treatment of early breast cancer and reported efficacy data according to HER2 status. Log hazard ratios (HRs) for disease-free and overall survival were pooled across the studies according to HER2 status by inverse variance weighting. A pooled test for treatment by HER2 status interaction was performed by weighted linear meta-regression. All statistical tests were two-sided.
Eight studies (with 6564 randomly assigned patients, of whom 5354 had HER2 status information available) were eligible for this analysis. In HER2-positive disease (n = 1536 patients), anthracyclines were superior to non-anthracycline-based regimens in terms of disease-free (pooled HR of relapse = 0.71; 95% confidence interval [CI] = 0.61 to 0.83; P < .001) and overall (pooled HR of death from any cause = 0.73; 95% CI = 0.62 to 0.85; P < .001) survival. In HER2-negative disease (n = 3818 patients), anthracyclines did not improve disease-free (HR = 1.00; 95% CI = 0.90 to 1.11; P = .75) or overall (HR = 1.03; 95% CI = 0.92 to 1.16; P = .60) survival. The test for treatment by HER2 status interaction yielded statistically significant results: for disease-free survival, the chi-square statistic for interaction was 13.7 (P < .001), and for overall survival, it was 12.6 (P < .001).
The added benefits of adjuvant chemotherapy with anthracyclines appear to be confined to women who have HER2 overexpressed or amplified breast tumors.
与非蒽环类辅助化疗方案相比,蒽环类辅助化疗可改善早期乳腺癌患者的无病生存期和总生存期。在随机临床试验中,通过亚组分析探讨了HER2状态作为蒽环类药物反应性标志物的作用,但结果并不一致。我们基于已发表的亚组数据,对HER2状态与蒽环类辅助化疗疗效之间的相互作用进行了汇总分析。
我们检索了文献数据库,以确定在早期乳腺癌治疗中比较蒽环类与非蒽环类辅助化疗方案的随机试验,并根据HER2状态报告疗效数据。根据HER2状态,通过逆方差加权对各研究中的无病生存期和总生存期的对数风险比(HR)进行汇总。通过加权线性meta回归对HER2状态相互作用的治疗进行汇总检验。所有统计检验均为双侧检验。
八项研究(共6564例随机分组患者,其中5354例有HER2状态信息)符合本分析要求。在HER2阳性疾病患者(n = 1536例)中,蒽环类药物在无病生存期(复发的汇总HR = 0.71;95%置信区间[CI] = 0.61至0.83;P <.001)和总生存期(任何原因导致死亡的汇总HR = 0.73;95% CI = 0.62至0.85;P <.001)方面优于非蒽环类方案。在HER2阴性疾病患者(n = 3818例)中,蒽环类药物并未改善无病生存期(HR = 1.00;95% CI = 0.90至1.11;P =.75)或总生存期(HR = 1.03;95% CI = 0.92至1.16;P =.60)。HER2状态相互作用的治疗检验产生了具有统计学意义的结果:对于无病生存期,相互作用的卡方统计量为13.7(P <.001),对于总生存期,为12.6(P <.001)。
蒽环类辅助化疗的额外益处似乎仅限于HER2过表达或扩增的乳腺肿瘤女性患者。