Evidence map›Paper›PMID 37298631›Full record

ReviewInternational journal of molecular sciences2023

Mechanisms of Resistance to Antibody-Drug Conjugates.

Rita Khoury, Khalil Saleh, Nadine Khalife, Mohamad Saleh, Claude Chahine, Rebecca Ibrahim, Axel Lecesne

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing 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

110 citing papers in PubMed.

  1. Review
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  9. Potency and safety of novel [British journal of cancer · 2026
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50 more citing papers are in PubMed but not listed here.

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

7 authors.

Rita KhouryInternational Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France.
Khalil SalehInternational Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France.
Nadine KhalifeDepartment of Head and Neck Oncology, Gustave Roussy Cancer Campus, 94800 Villejuif, France.
Mohamad SalehDepartment of Hematology and Oncology, Lebanese American University Medical Center-Rizk Hopsital, Beirut 1100, Lebanon.
Claude ChahineInternational Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France.
Rebecca IbrahimInternational Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France.
Axel LecesneInternational Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of cancer patients has dramatically changed over the past decades with the advent of monoclonal antibodies, immune-checkpoint inhibitors, bispecific antibodies, and innovative T-cell therapy. Antibody-drug conjugates (ADCs) have also revolutionized the treatment of cancer. Several ADCs have already been approved in hematology and clinical oncology, such as trastuzumab emtansine (T-DM1), trastuzumab deruxtecan (T-DXd), and sacituzumab govitecan (SG) for the treatment of metastatic breast cancer, and enfortumab vedotin (EV) for the treatment of urothelial carcinoma. The efficacy of ADCs is limited by the emergence of resistance due to different mechanisms, such as antigen-related resistance, failure of internalization, impaired lysosomal function, and other mechanisms. In this review, we summarize the clinical data that contributed to the approval of T-DM1, T-DXd, SG, and EV. We also discuss the different mechanisms of resistance to ADCs, as well as the ways to overcome this resistance, such as bispecific ADCs and the combination of ADCs with immune-checkpoint inhibitors or tyrosine-kinase inhibitors.

Indexed as

Carcinoma, Transitional CellImmunoconjugatesUrinary Bladder NeoplasmsAdo-Trastuzumab EmtansineHumansImmune Checkpoint InhibitorsAdo-Trastuzumab EmtansineImmune Checkpoint InhibitorsImmunoconjugatesantibody-drug conjugateenfortumab vedotinlinkermonoclonal antibodiespayloadsacituzumab govitecantrastuzumab deruxtecantrastuzumab emtasine

Identifiers

PMID37298631
PMCPMC10253543

What OpenQuestion holds

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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.