Antibody–Drug Conjugates in Non-small Cell Lung Cancer

Antibody-drug conjugates (ADCs) are complex molecules composed of a monoclonal antibody, a linker and a cytotoxic payload. Their design enables the selective delivery of cytotoxic agents to tumoral cells through antibody binding to a tumor-expressed antigen, followed by internalization, intracellular degradation and payload release, ultimately enabling the cytotoxic drug to exert its antitumor activity. ADCs have been evaluated in phase II and III trials in previously treated advanced non-small cell lung cancer (NSCLC), both in oncogene-addicted and in non-oncogene-addicted tumors, addressing resistance to standard therapies. Ongoing clinical trials are now expanding their use both in the first-line setting for advanced disease and in earlier disease stages. This narrative review summarizes the currently available data for ADC treatment in NSCLC, highlighting the need for improved patient selection to maximize benefit while limiting toxicity, incorporating clinical characteristics, pharmacogenomics and optimal treatment sequencing in the equation. Moreover, the understanding of resistance mechanisms and the development and validation of predictive biomarkers will be of utmost relevance to inform clinical practice.

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Publication Details

Journal
Drugs
Published
2026-05-18
DOI
https://doi.org/10.1007/s40265-026-02331-z
Primary Topic
HER2/EGFR in Cancer Research
Type
article
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0.00
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article

Antibody–Drug Conjugates in Non-small Cell Lung Cancer

Rob ter Heine, Martina Bortolot, Lodovica Zullo, Anna Sadowska et al.
Drugs
HER2/EGFR in Cancer Research
article

Antibody–Drug Conjugates in Non-small Cell Lung Cancer

Rob ter Heine, Martina Bortolot, Lodovica Zullo, Anna Sadowska, Stephanie P.L. Saw, Lizza Hendriks, Robin van Geel, Francesca R. Ogliari, Jordi Remon
article en

Abstract

Antibody-drug conjugates (ADCs) are complex molecules composed of a monoclonal antibody, a linker and a cytotoxic payload. Their design enables the selective delivery of cytotoxic agents to tumoral cells through antibody binding to a tumor-expressed antigen, followed by internalization, intracellular degradation and payload release, ultimately enabling the cytotoxic drug to exert its antitumor activity. ADCs have been evaluated in phase II and III trials in previously treated advanced non-small cell lung cancer (NSCLC), both in oncogene-addicted and in non-oncogene-addicted tumors, addressing resistance to standard therapies. Ongoing clinical trials are now expanding their use both in the first-line setting for advanced disease and in earlier disease stages. This narrative review summarizes the currently available data for ADC treatment in NSCLC, highlighting the need for improved patient selection to maximize benefit while limiting toxicity, incorporating clinical characteristics, pharmacogenomics and optimal treatment sequencing in the equation. Moreover, the understanding of resistance mechanisms and the development and validation of predictive biomarkers will be of utmost relevance to inform clinical practice.

Drugs
Radboud University Nijmegen (NL), Université Paris-Saclay (FR), Maastricht University Medical Centre (NL), Institut Gustave Roussy (FR), Radboud University Medical Center (NL), Radboud Institute for Molecular Life Sciences (NL), Centro di Riferimento Oncologico (IT), IRCCS Ospedale San Raffaele (IT), National Cancer Centre Singapore (SG), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Genoa (IT)
Openalex Percentile: Top 7%
HER2/EGFR in Cancer Research
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