Topoisomerase I inhibitor antibody–drug conjugates in breast cancer: the relevance of the DNA damage response to resistance, response, and combination treatment strategies

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Authors: Dayle K. Wang, Julia A. Steele, Susan R. Opalenik, Justin Micah Balko
Cited by: 1
References: 131

Abstract

INTRODUCTION: Antibody drug conjugates (ADCs) have revolutionized cancer treatment. ADCs that contain topoisomerase I inhibitors have been especially important in breast cancer treatment. Despite the substantial progress brought about by these ADCs, there remains a critical need to explore combination treatment strategies to overcome resistance and enhance the efficacy of these agents. Topoisomerase I inhibitors induce DNA damage and thus activate the DNA damage response (DDR). DDR elements have been examined in terms of their role in resistance and response to topoisomerase I inhibitors, and DDR inhibitors may be especially powerful when combined with topoisomerase I inhibitors. METHODS: This review will discuss the topoisomerase I inhibitor ADCs approved for breast cancer treatment, the relevance of select components of the DNA damage response to topoisomerase I inhibitor-containing therapies, and combination strategies with inhibitors of DNA damage response, specifically focusing on inhibitors of poly (ADP-ribose) polymerase (PARP) and the ataxia-telangiectasia mutated and Rad3-related (ATR) inhibitor. CONCLUSIONS: The introduction of topoisomerase inhibitors as an ADC payload into breast cancer care has redefined a need to better understand the intricacies of their mechanism of action and tumor methods of escape and resistance, hopefully leading to novel synergistic therapeutic strategies.

Fields of Study & Subjects

Cancer therapeutics and mechanisms PARP inhibition in cancer therapy HER2/EGFR in Cancer Research

Publication details

Journal / source
Breast Cancer Research and Treatment
Publisher
Springer Science and Business Media LLC
Volume
217
Issue
2
Publication date
17 April 2026
Language
EN