Navigating the Landscape of Resistance Mechanisms in Antibody-Drug Conjugates for Cancer Treatment
- PMID: 40234302
- DOI: 10.1007/s11523-025-01140-w
Navigating the Landscape of Resistance Mechanisms in Antibody-Drug Conjugates for Cancer Treatment
Abstract
Antibody-drug conjugates (ADCs) are an innovative approach in cancer therapy, combining the specificity of monoclonal antibodies (mAb) with the cytotoxic effect of chemotherapy agents. Despite the remarkable efficacy demonstrated in clinical studies, primary and secondary resistance to ADCs represent a concern and a significant challenge. Known resistance mechanisms mainly involve the targeted tumor antigen; the internalization, trafficking, and cleavage processes; the cytotoxic payload; and the intrinsic tumor cell dynamics of cell death and cell signaling. Key strategies to overcome these resistance mechanisms include the use of antibodies targeting the same antigen but with different payloads, developing dual-payload ADCs that target multiple cellular pathways, switching from non-cleavable to cleavable linkers, and combining ADCs with other therapies such as immune checkpoint inhibitors and antiangiogenic agents. By improving our understanding of what underlies the mechanisms of resistance to ADCs and implementing and studying systems to overcome these mechanisms, as well as using innovative therapeutic combinations, ADCs have the potential to continue to play a fundamental role in the treatment of tumors, especially refractory ones, providing patients with more effective and long-lasting therapeutic options, as well as better outcomes.
© 2025. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
Conflict of interest statement
Declarations. Funding: No external funding was used in the preparation of this manuscript. Conflicts of Interest: Domenica Lorusso: consulting or advisory role—PharmaMar, AstraZeneca, Clovis Oncology, GlaxoSmithKline, MSD, Genmab, Seagen, Immunogen, Oncoinvest, Corcept Therapeutics, and Sutro Biopharma, Novartis; speakers’ bureau—AstraZeneca, Clovis Oncology, GlaxoSmithKline, MSD, PharmaMar, ImmunoGen, Seagen, and Genmab; travel, accommodations, expenses—AstraZeneca, Clovis Oncology, GlaxoSmithKline. Giovanni Fucà: honoraria—AstraZeneca; travel, accommodations, expenses—GlaxoSmithKline. Giovanni Fucà is currently an employee of AstraZeneca; however, at the time of manuscript submission, Giovanni Fucà was not affiliated with AstraZeneca, and this affiliation had no role in the study design, data analysis, or manuscript preparation. Ilaria Sabatucci: former employee of AstraZeneca. Gloria Lalli, Mariachiara Paderno, Fabio Martinelli, Mauro Signorelli, Matteo Maruccio, and Giampaolo Di Martino declare that they have no conflicts of interest that might be relevant to the contents of this manuscript. Ethics Approval: Not applicable. Informed Consent: Not applicable. Consent to Publish: Not applicable. Data Availability Statement: Data described in this article was sourced from published works as cited throughout. Code Availability: Not applicable. Authors’ Contributions: Conceptualization: G.L., G.F., and D.L. Data curation: G.L., I.S., M.P., F.M., M.S., M.M., and G.D.P. Supervision: G.F. and D.L. Visualization: G.L. Writing—original draft: G.L., I.S., M.P., F.M., M.S., M.M., and G.D.M. Writing—review and editing: G.F. and D.L.
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