Neoadjuvant Trials in ER+ Breast Cancer: A Tool for Acceleration of Drug Development and Discovery

被引:26
|
作者
Guerrero-Zotano, Angel L.
Arteaga, Carlos L.
机构
[1] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Dept Med,Breast Canc Program, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Dept Canc Biol,Breast Canc Program, Nashville, TN USA
关键词
PRIMARY ENDOCRINE THERAPY; PHASE-II TRIAL; ESTROGEN-RECEPTOR; POSTMENOPAUSAL WOMEN; DOUBLE-BLIND; ELDERLY WOMEN; PREOPERATIVE WINDOW; RANDOMIZED-TRIAL; KI67; EXPRESSION; PLUS LETROZOLE;
D O I
10.1158/2159-8290.CD-17-0228
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neoadjuvant therapy trials offer an excellent strategy for drug development and discovery in breast cancer, particularly in triple-negative and HER2-overexpressing subtypes, where pathologic complete response is a good surrogate of long-term patient benefit. For estrogen receptor-positive (ER+) breast cancers, however, use of this strategy has been challenging because of the lack of validated surrogates of long-term efficacy and the overall good prognosis of the majority of patients with this cancer subtype. We review below the clinical benefits of neoadjuvant endocrine therapy for ER+/HER2-negative breast cancer, its use and limitations for drug development, prioritization of adjuvant and metastatic trials, and biomarker discovery. Significance: Neoadjuvant endocrine therapy is an excellent platform for the development of investigational drugs, triaging of novel combinations, biomarker validation, and discovery of mechanisms of drug resistance. This review summarizes the clinical and investigational benefits of this approach, with a focus on how to best integrate predictive biomarkers into novel clinical trial designs. (C) 2017 AACR.
引用
收藏
页码:561 / 574
页数:14
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