Evidence map›Paper›PMID 41630503›Full record

ReviewThe oncologist2026

Overcoming resistance to antibody-drug conjugates: mechanisms and emerging strategies.

Aki Inase, Shiro Kimbara, Eli Imamura, Mitch A Phelps, Hironobu Minami

Abstract readReview
In one paragraph

Review in The oncologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Aki InaseDivision of Medical Oncology and Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Kobe, 650-0017, Japan.ORCID 0000-0002-6718-3433
Shiro KimbaraDivision of Medical Oncology and Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Kobe, 650-0017, Japan.
Eli ImamuraTimele Clinic, Tokyo, 167-0022, Japan.
Mitch A PhelpsDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH, 43210, United States.ORCID 0000-0002-1615-5280
Hironobu MinamiDivision of Medical Oncology and Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Kobe, 650-0017, Japan.

Funding

The Chesapeake-Ohio Pharmacokinetics Core for The ETCTNU24CA247648 · NCI · JOHNS HOPKINS UNIVERSITY · PI Jan Hendrik Beumer, Mitch A Phelps · 2020 to 2026
$3.6M
Cachexia-mediated FcRn Modulation and Its Impact on Anti-PD1 Therapy in Lung CancerR01CA273924 · NCI · OHIO STATE UNIVERSITY · PI COSS, CHRISTOPHER C., MACE, THOMAS A · 2022 to 2025
$3.1M
NCI NIH HHS R01CA273924NCI NIH HHS U24CA247648
6 · The paper itself

Abstract

backgroundAntibody-drug conjugates (ADCs) combine a tumor antigen-specific monoclonal antibody with a cytotoxic payload via a linker, enabling selective delivery of cytotoxic agents to cancer cells while minimizing damage to healthy tissues. This approach has revolutionized cancer treatment; however, despite these advantages, resistance to ADCs has emerged as a significant barrier to long-term efficacy.

methodsIn this review, we summarize and analyze molecular pathways implicated in ADC resistance across multiple cancer types, including triple-negative breast cancer, non-small cell lung cancer, pancreatic cancer, and relapsed/refractory acute myeloid leukemia. We further examine emerging strategies to overcome resistance, with particular emphasis on combination therapies and the development of next-generation ADCs.

resultsAccumulating evidence indicates that identifying and targeting key resistance-associated pathways can expand the population of patients who benefit from ADC therapy and extend the therapeutic lifespan of these agents. We highlight representative preclinical studies that have elucidated resistance mechanisms and demonstrate potential approaches to restore or enhance ADC efficacy.

conclusionUnderstanding and overcoming ADC resistance is essential as these agents continue to expand into new therapeutic settings. By bridging basic mechanistic insights with translational and preclinical evidence, this review provides a comprehensive framework for addressing ADC resistance and informs future strategies for optimizing cancer treatment.

Indexed as

Drug Resistance, NeoplasmImmunoconjugatesNeoplasmsAnimalsAntibodies, MonoclonalHumansAntibodies, MonoclonalImmunoconjugatesADC resistanceantibody–drug conjugatescombination therapynext-generation ADCspreclinical studiesresistance mechanisms

Identifiers

PMID41630503
PMCPMC13007285

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.