How I treat endocrine-dependent metastatic breast cancer

被引:16
作者
Gombos, A. [1 ]
Goncalves, A. [2 ]
Curigliano, G. [3 ]
Bartsch, R. [4 ]
Kyte, J. A. [5 ]
Ignatiadis, M. [1 ]
Awada, A. [1 ,6 ]
机构
[1] Univ Libre Bruxelles, Dept Med Oncol, Inst Jules Bordet, Brussels, Belgium
[2] Aix Marseille Univ, Inst Paoli Calmettes, Ctr Rech Cancyrol Marseille CRCM, Inserm U1068,CNRS U7258, Marseille, France
[3] Univ Milan, European Inst Oncol, Milan, Italy
[4] Med Univ Vienna, Dept Med 1, Vienna, Austria
[5] Oslo Univ Hosp, Dept Oncol, Oslo, Norway
[6] Rue Meylemeersch 90,1070, B-1070 Brussels, Belgium
关键词
luminal breast cancer; CDK; 4; 6; PIK3CA; SERD; antibodyedrug conjugate (ADC); ESTROGEN-RECEPTOR DEGRADER; CELL-FREE DNA; PHASE-III; PATIENTS PTS; SACITUZUMAB GOVITECAN; PLUS FULVESTRANT; PIK3CA MUTATIONS; ESR1; MUTATIONS; MONARCH; PALBOCICLIB;
D O I
10.1016/j.esmoop.2023.100882
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Estrogen receptor-positive (ER+)/HER2-negative (HER2-), the so-called luminal-type breast cancer, is the most frequent subset, accounting for around 70% of all breast cancer cases. Endocrine therapy (ET) combined with cyclin-dependent kinases (CDK) 4/6 inhibitors is the standard first option in the management of advanced luminal breast cancer independently of disease extension. Classically, patients undergo multiple lines of ET + targeted treatments until endocrine resistance occurs and palliative chemotherapy is proposed. Understanding endocrine resistance mechanisms and development of novel ET options is one of the main challenges in current clinical research. Another area of utmost interest is the improvement of post-endocrine therapeutic approaches. Among others, the development of antibodyedrug conjugates (ADCs) is very promising, and some of these drugs will probably soon become a part of the therapeutic arsenal against this incurable disease. This review paper provides an overview of currently available treatment options in ER+/HER2- metastatic breast cancer and extensively discusses new approaches in late clinical development.
引用
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页数:13
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