New Strategies in Metastatic Hormone Receptor-Positive Breast Cancer: Searching for Biomarkers to Tailor Endocrine and Other Targeted Therapies

被引:10
作者
Jankowitz, Rachel C. [1 ,2 ,3 ,4 ]
Oesterreich, Steffi [2 ,3 ,4 ,5 ,6 ]
Lee, Adrian V. [2 ,3 ,4 ,5 ,6 ]
Davidson, Nancy E. [1 ,2 ,3 ,4 ,5 ,7 ,8 ]
机构
[1] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Womens Canc Res Ctr, Pittsburgh, PA USA
[3] Magee Womens Res Inst, Pittsburgh, PA USA
[4] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
[5] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA USA
[6] Univ Pittsburgh, Dept Human Genet, Pittsburgh, PA USA
[7] Fred Hutchinson Canc Res Ctr, 1100 Fairview Ave North,Thomas Bldg,M-S D5-310, Seattle, WA 98104 USA
[8] Univ Washington, 1100 Fairview Ave North,Thomas Bldg,M-S D5-310, Seattle, WA 98109 USA
关键词
CIRCULATING TUMOR-CELLS; ESR1; MUTATIONS; AMERICAN SOCIETY; PROGNOSTIC VALUE; POOLED ANALYSIS; DOUBLE-BLIND; FREE DNA; LETROZOLE; MULTICENTER; PALBOCICLIB;
D O I
10.1158/1078-0432.CCR-16-0591
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although major advances in our understanding of the molecular underpinnings of hormone receptor-positive (HR+) breast cancer have led to new therapies that have substantially improved patient outcomes, endocrine-resistant disease still remains a leading cause of breast cancer mortality. Comprehensive molecular profiling of breast cancers has highlighted tremendous tumor heterogeneity, and analysis of paired primary and metastatic tumors has shown the evolution that can occur during acquired resistance to systemic therapies. Novel techniques for monitoring tumor load under treatment pressure, including "liquid biopsy" techniques, such as circulating free tumor DNA (cfDNA) and circulating tumor cells, have shown promise as biomarkers to direct treatment without invasive tumor biopsies. However, more research is needed to deepen our understanding of breast cancer alterations under treatment pressure to reveal mechanisms of drug resistance and apply precision medicine in biomarker-driven clinical trials. (C)2016 AACR.
引用
收藏
页码:1126 / 1131
页数:6
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