McAndrew Nicholas, DeMichele Angela
Department of Medicine, Division of Hematology/Oncology at the University of Pennsylvania.
Department of Medicine, Division of Hematology/Oncology at the University of Pennsylvania; Also at the Abramson Cancer Center, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania.
J Target Ther Cancer. 2018 Feb;7(1):52-69. Epub 2018 Feb 14.
The optimal neoadjuvant chemotherapy (NACT) regimen in triple-negative breast cancer (TNBC) has not been clearly defined. Achieving a pathologic complete response (pCR) provides important prognostic information, and, especially in TNBC, is considered a surrogate endpoint for event-free survival. Thus, many neoadjuvant studies in TNBC focus on this as a primary endpoint, and such information may be used for accelerated US Food and Drug Administration approval. Current controversies in the field include: (1) the role of platinum-based compounds; (2) the optimal chemotherapy backbone; and (3) the benefits of additional therapy after surgery. Conflicting results of 2 major studies adding carboplatin to NACT have highlighted the need to balance potential benefits to disease outcomes against increased toxicity. While the PROGECT study suggests efficacy of a nonanthracycline-containing regimen, this is observational data, and evidence in the form of a clinical trial remains to be seen. Data surrounding optimal taxane use support the use of nab-paclitaxel in place of paclitaxel in limited clinical situations. Although bevacizumab may increase pCR rates, this has not translated into survival benefit. Capecitabine shows promise in patients who have not achieved pCR after NACT. The neoadjuvant setting remains an important model for drug development. This review will focus on the most important and most current neoadjuvant trials in women with TNBC.
三阴性乳腺癌(TNBC)的最佳新辅助化疗(NACT)方案尚未明确界定。实现病理完全缓解(pCR)可提供重要的预后信息,尤其是在TNBC中,被视为无事件生存期的替代终点。因此,许多TNBC的新辅助研究将此作为主要终点,此类信息可用于加速美国食品药品监督管理局的批准。该领域当前的争议包括:(1)铂类化合物的作用;(2)最佳化疗主干方案;(3)术后辅助治疗的益处。两项将卡铂添加到NACT中的大型研究结果相互矛盾,凸显了在疾病预后潜在益处与毒性增加之间取得平衡的必要性。虽然PROGECT研究表明不含蒽环类药物方案的疗效,但这是观察性数据,临床试验形式的证据仍有待观察。关于最佳紫杉烷使用的数据支持在有限的临床情况下使用白蛋白结合型紫杉醇替代紫杉醇。尽管贝伐单抗可能会提高pCR率,但这并未转化为生存获益。卡培他滨在NACT后未达到pCR的患者中显示出前景。新辅助治疗环境仍然是药物研发的重要模型。本综述将聚焦于TNBC女性患者中最重要和最新的新辅助试验。