Antibody-drug conjugates (ADCs) have transitioned from experimental constructs to a clinically validated therapeutic class, with a rapidly expanding portfolio of approvals across hematologic and solid malignancies. Despite this success, most ADC development programs continue to fail, particularly in solid tumors, underscoring a persistent gap between molecular design and clinical performance.

This review argues that payload potency, long regarded as the primary determinant of ADC efficacy, is no longer the principal limitation. Instead, clinical outcomes are increasingly governed by system-level interactions among antibody distribution, linker kinetics, payload diffusibility, tumor heterogeneity, and host toxicity mechanisms. We synthesize mechanistic, pharmacologic, and clinical evidence across constraint-driven design shifts of ADC development to identify the design inflection points that have genuinely altered therapeutic indices.

We further evaluate why high-drug-to-antibody ratio constructs, bystander-capable payloads, and site-specific conjugation strategies have succeeded where earlier generations failed. Finally, we outline emerging next-generation paradigms, including mutant-selective targeting, bispecific architectures, and dual-payload ADCs, that reframe ADCs as adaptable platforms rather than static cytotoxic delivery vehicles. By integrating molecular engineering with tumor biology and clinical constraints, this review proposes a design framework to guide the next decade of ADC innovation in oncology.

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Authors: Shahin Javanmard1, Merve Nur Güven2

Authors: 1 Internal Medicine Department, Inonu University Turgut Ozal Medical Center, Turkey (corresponding author); 2 Radiation Oncology Department, Hatay Training and Research Hospital, Turkey

Key terms: Antibody-drug conjugates (ADCs); targeted oncology; linker-payload engineering; drug-to-antibody ratio; tumor heterogeneity; next-generation ADCs

Published In: ADC Review| Journal of Antibody-drug Conjugates

DOI: 10.14229/jadc.2026.27.03.001.


How to cite:

Javanmard S and Nur Güven M  Antibody-Drug Conjugates in Oncology: Why Potency Is No Longer the Limiting Factor – J. ADC. March 27, 2026. DOI: 10.14229/jadc.2026.27.03.001.


Final Editorial Review: March 23, 2026

History:

  • Original Manuscript Received: March 4, 2026
  • Review results received: March 11, 2026
  • Manuscript accepted for publication: March 25, 2026
  • Article published online: March 27, 2026

Conflict of Interest
The author does not have any competing interests.

Featured image Unsplash © 2020 – 2026  Used with permission.


© 2026 The Authors. Used with permission.

DOI: 10.14229/jadc.2026.27.03.001.

 

 

 

 

 

 

 

 

Lonza 2025|26 May 2026
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