Dhesy-Thind Bindi, Pritchard Kathleen I, Messersmith Hans, O'Malley Frances, Elavathil Leela, Trudeau Maureen
Juravinski Cancer Centre, Hamilton, ON, Canada.
Breast Cancer Res Treat. 2008 May;109(2):209-29. doi: 10.1007/s10549-007-9656-y. Epub 2007 Jul 17.
Amplification and/or overexpression of the HER2/neu gene is associated with a poor prognosis in breast cancer. Many studies have suggested that this gene may be associated with the relative efficacy of chemotherapy and endocrine therapy options.
A systematic review of the evidence was conducted. MEDLINE, EMBASE, the Cochrane Library, the American Society of Clinical Oncology annual meeting proceedings, and the San Antonio Breast Cancer Symposia proceedings were all searched to November 2006 for reports of analysis by HER2/neu status of the relative efficacy of the treatment arms in randomized controlled trials.
Thirty-five trials were identified. A meta-analysis of trials of tamoxifen versus observation found no significant interaction between treatment and HER2/neu status, although one trial not included in the meta-analysis did find interaction. A meta-analysis of adjuvant anthracycline-based chemotherapy trials found a significant interaction (difference in disease-free survival log-hazard ratios -0.31, 95% confidence interval -0.50 to -0.13; difference in overall survival log-hazard ratios -0.34, 95% confidence interval -0.53 to -0.14). Significant interaction was also found in a meta-analysis of disease-free survival in trials of adjuvant taxane therapy versus non-taxane therapy (difference in disease-free survival log-hazard ratios -0.36, 95% confidence interval -0.68 to -0.04). HER2/neu overexpression and/or amplification was associated with greater efficacy of the anthracycline or taxane regimen.
Current evidence supports the conclusion that the benefit of both anthracycline-based and taxane-based adjuvant chemotherapy is associated on HER2/neu status, with patients with HER2/neu-positive cancers benefiting more from these therapies than those with HER2/neu-negative cancers.
HER2/neu基因的扩增和/或过表达与乳腺癌预后不良相关。许多研究表明,该基因可能与化疗和内分泌治疗方案的相对疗效有关。
对证据进行了系统评价。检索了MEDLINE、EMBASE、Cochrane图书馆、美国临床肿瘤学会年会论文集以及圣安东尼奥乳腺癌研讨会论文集,直至2006年11月,以查找关于随机对照试验中治疗组相对疗效的HER2/neu状态分析报告。
共确定了35项试验。对他莫昔芬与观察对照试验的荟萃分析发现,治疗与HER2/neu状态之间无显著交互作用,尽管一项未纳入荟萃分析的试验确实发现了交互作用。对基于蒽环类药物的辅助化疗试验的荟萃分析发现存在显著交互作用(无病生存对数风险比差异为-0.31,95%置信区间为-0.50至-0.13;总生存对数风险比差异为-0.34,95%置信区间为-0.53至-0.14)。在辅助紫杉烷治疗与非紫杉烷治疗试验的无病生存荟萃分析中也发现了显著交互作用(无病生存对数风险比差异为-0.36,95%置信区间为-0.68至-0.04)。HER2/neu过表达和/或扩增与蒽环类或紫杉烷方案的疗效更佳相关。
现有证据支持以下结论,即基于蒽环类和紫杉烷类的辅助化疗的益处与HER2/neu状态相关,HER2/neu阳性癌症患者比HER2/neu阴性癌症患者从这些治疗中获益更多。