Selective Estrogen Receptor Degraders (SERDs)

被引:0
作者
Taylor, Melissa [1 ,2 ]
Kahn, Adriana [1 ,2 ]
Foldi, Julia [3 ,4 ]
机构
[1] Yale Univ, Sch Med, Sect Med Oncol, New Haven, CT 06510 USA
[2] Yale Canc Ctr, New Haven, CT 06510 USA
[3] Univ Pittsburgh, Div Hematol Oncol, Sch Med, 300 Halket St,Suite 3524, Pittsburgh, PA 15213 USA
[4] UPMC, Hillman Canc Ctr, 300 Halket St,Suite 3524, Pittsburgh, PA 15213 USA
关键词
Hormone receptor positive breast cancer; Endocrine therapy; Estrogen receptor; Selective estrogen receptor degraders; ADVANCED BREAST-CANCER; FULVESTRANT; 500; MG; ANASTROZOLE; POSTMENOPAUSAL WOMEN; PHASE-II; ENDOCRINE THERAPIES; 1ST-LINE TREATMENT; SURVIVAL ANALYSIS; DOSE-ESCALATION; DOUBLE-BLIND;
D O I
10.1007/s12609-024-00563-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of ReviewUpdate on the most recent clinical evidence on selective estrogen receptor degraders (SERDs) in the treatment of hormone receptor (HR)-positive (HR +), human epidermal growth factor receptor 2 (HER2)-negative (HER2-) breast cancer.Recent FindingsDespite effective endocrine therapies, resistance commonly develops during treatment of HR + breast cancer and mutations in ESR1 account for a large proportion of resistance mechanisms. After demonstration of the superior efficacy of fulvestrant in ESR1-mutated tumors, recent advances allowed the development of a novel class of orally bioavailable selective estrogen receptor degraders (SERDs), which are beginning to revolutionize the field. The first approved oral SERD, elacestrant, is currently used in the second-line treatment of HR + /HER2- metastatic breast cancer, and a number of other oral SERDs are undergoing clinical evaluation in both the metastatic and early-stage settings.SummarySERDs are a rapidly developing class of antiestrogens that show activity in treatment of tumors harboring ESR1 mutations associated with resistance to earlier generations of endocrine therapy, but knowledge gaps remain, and further research is necessary to better define their optimal use.
引用
收藏
页码:402 / 416
页数:15
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