Tyrosine kinase inhibitors in HER2-positive metastatic breast cancer with trastuzumab emtansine resistance: insights from a multicenter retrospective real-world study

MedComm ›› 2024, Vol. 5 ›› Issue (7) : e624

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MedComm ›› 2024, Vol. 5 ›› Issue (7) :e624 DOI: 10.1002/mco2.624
ORIGINAL ARTICLE

Tyrosine kinase inhibitors in HER2-positive metastatic breast cancer with trastuzumab emtansine resistance: insights from a multicenter retrospective real-world study

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Abstract

The use of trastuzumab emtansine (T-DM1) has revealed significant efficacy in HER2-positive metastatic breast cancer (MBC). However, optimal therapeutic strategies following T-DM1 failure remain a subject of debate in clinical practice. In this multicenter, retrospective, real-world study, we sought to examine the effectiveness and safety of tyrosine kinase inhibitors (TKIs) as a therapeutic strategy in HER2-positive MBC who developed T-DM1 resistance. Between September 2018 and December 2022, 66 patients were enrolled. The median progression-free survival of TKIs-based therapy was 10.1 months (95% CI, 4.7–15.6). Objective response rate and clinical benefit rate were 18.2 and 66.7%, respectively. TKIs-based therapy demonstrated better effectiveness in patients who had previously derived benefit from T-DM1 and featured acquired resistance to trastuzumab. The most common adverse events were diarrhea (36, 54.5%), hand-foot syndrome (31, 47.0%), and leucopenia (30, 45.5%). In conclusion, TKIs-based therapy showed promising effectiveness and safety in HER2-positive MBC patients after T-DM1 failure.

Keywords

HER2-positive breast cancer / real-world study / trastuzumab emtansine resistance / tyrosine kinase inhibitors

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Chunxiao Sun, Yijia Hua, Nan Jin, Xiaojia Wang, Jian Huang, Xinyu Wu, Tianyu Zeng, Xueqi Yan, Fan Yang, Yan Liang, Xiang Huang, Wei Li, Yongmei Yin. Tyrosine kinase inhibitors in HER2-positive metastatic breast cancer with trastuzumab emtansine resistance: insights from a multicenter retrospective real-world study. MedComm, 2024, 5(7): e624 DOI:10.1002/mco2.624

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