Antibody–drug conjugates in cancer therapy: current landscape, challenges, and future directions

Antibody-drug conjugates (ADCs) have emerged as a transformative modality in oncology by combining the target specificity of antibodies with the high potency of diverse cytotoxic payloads. This review provides an integrative overview of ADCs, spanning from molecular design to clinical translation. We dissect the structural components, antibodies, linkers, and payloads, and elucidate their impact on pharmacokinetics, tumor selectivity, and therapeutic index. Mechanistic pathways, including antigen recognition, receptor-mediated internalization, payload release, and immunogenic cell death (ICD), are highlighted to provide context for ADC function. Clinically, ADCs have demonstrated efficacy across hematologic and solid malignancies, with 15 Food and Drug Administration (FDA) approvals and an expanding investigational pipeline. However, challenges persist, including antigen heterogeneity, resistance mechanisms, systemic toxicities, and manufacturing complexities. Emerging innovations such as bispecific ADCs, immune-stimulatory payloads, AI-guided design, and nanotechnology-enhanced delivery are reshaping the ADC landscape. Finally, we emphasize the necessity of diagnostic precision and rational combination strategies, while highlighting emerging innovations that collectively shape the future direction of next-generation ADC therapeutics.

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Publication Details

Journal
Molecular Cancer
Published
2025-11-03
DOI
https://doi.org/10.1186/s12943-025-02489-2
Citations
14
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
14.64

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article

Antibody–drug conjugates in cancer therapy: current landscape, challenges, and future directions

Ka‐Fai To, William Ka Kei Wu, Bonan Chen, Gary Man-Kit Tse et al.
14 citations
Molecular Cancer
HER2/EGFR in Cancer Research
14.64
article

Antibody–drug conjugates in cancer therapy: current landscape, challenges, and future directions

Ka‐Fai To, William Ka Kei Wu, Bonan Chen, Gary Man-Kit Tse, Wei Kang, Jialin Wu, Jun Qing Yu, Guoming Chen, Yi Xu, Xiaohong Zheng
article en
14 citations

Abstract

Antibody-drug conjugates (ADCs) have emerged as a transformative modality in oncology by combining the target specificity of antibodies with the high potency of diverse cytotoxic payloads. This review provides an integrative overview of ADCs, spanning from molecular design to clinical translation. We dissect the structural components, antibodies, linkers, and payloads, and elucidate their impact on pharmacokinetics, tumor selectivity, and therapeutic index. Mechanistic pathways, including antigen recognition, receptor-mediated internalization, payload release, and immunogenic cell death (ICD), are highlighted to provide context for ADC function. Clinically, ADCs have demonstrated efficacy across hematologic and solid malignancies, with 15 Food and Drug Administration (FDA) approvals and an expanding investigational pipeline. However, challenges persist, including antigen heterogeneity, resistance mechanisms, systemic toxicities, and manufacturing complexities. Emerging innovations such as bispecific ADCs, immune-stimulatory payloads, AI-guided design, and nanotechnology-enhanced delivery are reshaping the ADC landscape. Finally, we emphasize the necessity of diagnostic precision and rational combination strategies, while highlighting emerging innovations that collectively shape the future direction of next-generation ADC therapeutics.

Molecular CancerVol. 24(1)
Guangzhou University of Chinese Medicine (CN), Harbin Medical University (CN), Chinese University of Hong Kong (HK), HKUST Shenzhen Research Institute (CN), City University of Hong Kong, Shenzhen Research Institute (CN), Second Affiliated Hospital of Harbin Medical University (CN), University of Hong Kong (HK)
National Natural Science Foundation of China, Chinese University of Hong Kong
Openalex Percentile: Top 1%
HER2/EGFR in Cancer Research
14.64
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