Evidence map›Paper›PMID 41427810›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2026

Predictive Biomarkers of Antibody-Drug Conjugate Efficacy for Solid Tumors: Current Challenges and the Potential Role of Quantitative Proteomics.

Nicholas J McNamee, Jia Liu, Rebecca C Poulos, Adel T Aref, Roger R Reddel

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 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.

Nicholas J McNameeProCan, Children's Medical Research Institute, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.ORCID 0000-0003-0267-9179
Jia LiuThe Kinghorn Cancer Centre, St. Vincent's Hospital, Sydney, Australia.ORCID 0000-0003-4442-6516
Rebecca C PoulosProCan, Children's Medical Research Institute, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.ORCID 0000-0002-8419-7028
Adel T ArefProCan, Children's Medical Research Institute, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.ORCID 0000-0003-3028-131X
Roger R ReddelProCan, Children's Medical Research Institute, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.ORCID 0000-0002-6302-6107

Funding

Australian Cancer Research Foundation (ACRF)Cancer Council NSW (Cancer Council New South Wales) IG 18-01Cancer Institute NSW (Cancer Institute New South Wales) (2017/TPG001Cancer Institute NSW (Cancer Institute New South Wales) 2021/CBG0002Cancer Institute NSW (Cancer Institute New South Wales) REG171150)Faculty of Medicine and Health, University of Sydney (Faculty of Medicine and Health)Ian Potter Foundation (IPF)Medical Research Future Fund (MRFF)National Breast Cancer Foundation (NBCF) IIRS-18-164National Health and Medical Research Council (NHMRC) GNT1170739NSW Health (The NSW Health) CMP-01Royal Australasian College of Physicians (RACP)
6 · The paper itself

Abstract

Antibody-drug conjugate (ADC) development is progressing rapidly, with significant impacts on the treatment landscape of clinical oncology. However, the development of predictive biomarkers to guide ADC selection has not kept pace and to date has been mostly limited to immunohistochemistry, hampering patient selection and personalized treatment recommendations. Here, we review the current state of ADC target protein assessment and the association between target expression levels and therapeutic efficacy. We discuss the limitations and challenges of existing protein assessment technology and highlight the potential clinical role of quantitative mass spectrometry-based proteomics for rapid, comprehensive, and accurate protein quantification. We propose that integrating multiplexed proteomic assays early in ADC development and clinical trial design can improve therapeutic targeting, enhance clinical trial design, and ultimately lead to more personalized ADC-based treatment strategies.

Indexed as

Biomarkers, TumorImmunoconjugatesNeoplasmsProteomicsHumansBiomarkers, TumorImmunoconjugates

Identifiers

PMID41427810
PMCPMC13043171

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.