CDK4/6 inhibitor resistance in estrogen receptor positive breast cancer, a 2023 perspective

被引:20
|
作者
Zhou, Fiona H. [1 ,2 ]
Downton, Teesha [1 ,2 ]
Freelander, Allegra [1 ,2 ]
Hurwitz, Joshua [1 ,2 ]
Caldon, C. Elizabeth [1 ,2 ]
Lim, Elgene [1 ,2 ]
机构
[1] Garvan Inst Med Res, Sydney, NSW, Australia
[2] Univ NSW, St Vincents Clin Sch, Sydney, NSW, Australia
关键词
estrogen receptor; breast cancer; CDK4/6; inhibitor; endocrine therapy; resistance; DEPENDENT KINASE 4/6; FULVESTRANT PLUS CAPIVASERTIB; PHYSICIANS CHOICE TPC; PATIENTS PTS; OPEN-LABEL; PHASE-II; AROMATASE INHIBITOR; SACITUZUMAB GOVITECAN; ACQUIRED-RESISTANCE; ENDOCRINE THERAPY;
D O I
10.3389/fcell.2023.1148792
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CDK4/6 inhibitors have become game-changers in the treatment of estrogen receptor-positive (ER+) breast cancer, and in combination with endocrine therapy are the standard of care first-line treatment for ER+/HER2-negative advanced breast cancer. Although CDK4/6 inhibitors prolong survival for these patients, resistance is inevitable and there is currently no clear standard next-line treatment. There is an urgent unmet need to dissect the mechanisms which drive intrinsic and acquired resistance to CDK4/6 inhibitors and endocrine therapy to guide the subsequent therapeutic decisions. We will review the insights gained from preclinical studies and clinical cohorts into the diverse mechanisms of CDK4/6 inhibitor action and resistance, and highlight potential therapeutic strategies in the context of CDK4/6 inhibitor resistance.
引用
收藏
页数:12
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