HER2 heterogeneity and resistance to anti-HER2 antibody-drug conjugates

被引:67
|
作者
Ocana, Alberto [1 ,2 ,3 ,4 ]
Amir, Eitan [5 ,6 ]
Pandiella, Atanasio [3 ,7 ,8 ]
机构
[1] Hosp Clin San Carlos, Med Oncol Dept, Expt Therapeut Unit, Madrid, Spain
[2] IdISSC, Madrid, Spain
[3] Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain
[4] Castilla La Mancha Univ UCLM, Ctr Reg Invest Biorned, Albacete, Spain
[5] Princess Margaret Canc Ctr, Dept Med, Div Med Oncol & Hematol, Toronto, ON, Canada
[6] Univ Toronto, Toronto, ON, Canada
[7] IBMCC, Salamanca, Spain
[8] IBSAL, Salamanca, Spain
关键词
HER2; heterogeneity; resistance; ADCs; T-DM1; DS-8201; SURVIVAL; CANCER; TUMORS;
D O I
10.1186/s13058-020-1252-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There has been substantial interest in HER2 intratumoral heterogeneity as an explanation for the development of resistance to anti-HER2 therapies in breast cancer, particularly to trastuzumab emtansine (T-DM1). Methods: Through a literature-based approach, we discuss mechanisms of resistance to HER2-targeting antibody-drug conjugates (ADCs) in breast cancer. Results: We describe results from clinical studies reporting the effect of anti-HER2 strategies particularly ADCs and their mechanistic effect. We review biological findings underlying HER2 heterogeneity and its implication in the development of novel anti-HER2 drugs including new ADCs in clinical development like trastuzumab deruxtecan (DS-8201). Conclusions: We suggest potential mechanisms to optimize these compounds and their future clinical implementation.
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页数:3
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