Evidence map›Paper›PMID 40550567›Full record

ArticleJournal for immunotherapy of cancer2025

SITC perspective: leveraging patient enrichment biomarkers to accelerate early phase IO drug development.

Leisha A Emens, Christine Moussion, Patrick Hwu, James L Gulley, Pamela S Ohashi, Carlo B Bifulco, David Feltquate

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
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  5. 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

7 authors.

Leisha A EmensKaiser Permanente, South Sacramento, California, USA emensle@icloud.com.
Christine MoussionGenentech, South San Francisco, California, USA.
Patrick HwuH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.ORCID http://orcid.org/0000-0002-8293-1313
James L GulleyNCI, National Institutes of Health, Bethesda, Maryland, USA.ORCID http://orcid.org/0000-0002-6569-2912
Pamela S OhashiPrincess Margaret Hospital Cancer Centre, Toronto, Ontario, Canada.
Carlo B BifulcoProvidence Portland Medical Center, Earle A. Chiles Research institute, Portland, Oregon, USA.
David FeltquateiTeos Therapeutics Inc, Watertown, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy (IO) enables patients to live well with cancer for many years, or even be cured. Several investigational IO agents recently failed in early-phase or late-phase trials, leading some to doubt the future of IO. Patient heterogeneity (eg, tumor characteristics, treatment history) increases the risk that a clinically active IO drug might be discarded. Enriching enrollment for patients with biomarkers hypothesized to reflect a higher probability of clinical benefit across clinical development should mitigate this risk. The Society for Immunotherapy of Cancer convened diverse IO stakeholders to discuss leveraging biomarkers at the earliest stages of drug development to accelerate the delivery of innovative IO agents to patients. This group developed a framework based on a biomarker-based enrichment strategy in early trials that evolves into the development of more precise predictive biomarkers in late phase trials. This framework integrates mechanistic insights related to the drug and its impact on the tumor microenvironment derived from preclinical data, digital pathology, exploratory multiomics, and artificial intelligence that are continuously refined through both adaptive and randomized clinical trials. Biomarker-based enrichment in early clinical development should de-risk late-stage trials, ultimately expanding the portfolio of innovative IO drugs available to patients.

Indexed as

Biomarkers, TumorDrug DevelopmentImmunotherapyNeoplasmsHumansBiomarkers, TumorBiomarkerBiopsyNext generation sequencing - NGSPathologyTumor Microenvironment

Identifiers

PMID40550567
PMCPMC12184391

What OpenQuestion holds

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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.