Evidence map›Paper›PMID 41999755›Full record

ArticleMed (New York, N.Y.)2026

Impact of baseline medications on real-world overall survival in immune checkpoint inhibitor-treated patients with cancer in the RADIOHEAD cohort.

Samantha Stone, Muhammad Zaki Fadlullah, Yuxin Zhao, Enjun Yang, Jordan McPherson, Roberta Florido, Grace Watkins, Aik Choon Tan, John E Connolly, Ben J Brintz and 3 more

Abstract read
In one paragraph

Article in Med (New York, N.Y.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Samantha StoneHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA; Department of Pathology, University of Utah, Salt Lake City, UT, USA.
Muhammad Zaki FadlullahHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA; Department of Oncological Sciences, University of Utah, Salt Lake City, UT, USA.
Yuxin ZhaoHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Enjun YangParker Institute for Cancer Immunotherapy, San Francisco, CA, USA.
Jordan McPhersonHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA; Department of Pharmacy, University of Utah, Salt Lake City, UT, USA.
Roberta FloridoDivision of Cardiovascular Medicine, University of Utah, Salt Lake City, UT, USA.
Grace WatkinsHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Aik Choon TanHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA; Department of Oncological Sciences, University of Utah, Salt Lake City, UT, USA.
John E ConnollyParker Institute for Cancer Immunotherapy, San Francisco, CA, USA.
Ben J BrintzDivision of Epidemiology, University of Utah, Salt Lake City, UT, USA.
Samantha I LiangParker Institute for Cancer Immunotherapy, San Francisco, CA, USA.
Zoe QuandtDiabetes Center, University of California, San Francisco, San Francisco, CA, USA; Division of Endocrinology and Metabolism, Department of Medicine, San Francisco, CA, USA.
Arabella YoungHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA; Department of Pathology, University of Utah, Salt Lake City, UT, USA. Electronic address: arabella.young@hci.utah.edu.

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Huntsman Cancer Institute (HCI) Cancer Genetics, Epigenetics, Models, and Signaling (Cancer GEMS) Training ProgramT32CA265782 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Donald E Ayer, Sheri L Holmen · 2023 to 2026
$1.0M
Developing strategies to inhibit cancer immunotherapy-induced immune-related adverse events without impeding anti-tumor immunityR00CA246061 · NCI · UNIVERSITY OF UTAH · PI YOUNG, ARABELLA · 2022 to 2024
$747k
NCI NIH HHS P30 CA042014NCI NIH HHS R00 CA246061NCI NIH HHS T32 CA265782
6 · The paper itself

Abstract

backgroundThe benefits of immune checkpoint inhibitors (ICIs) observed in clinical trials often fail to translate to patients with cancer treated in a real-world setting. The identification of modifiable or monitorable exposures, such as baseline medication status, that may influence patient outcomes is necessary to reconcile disparities between clinical trial and real-world ICI efficacy.

methodsWe analyzed baseline medication use obtained through electronic data capture (EDC) from the real-world RADIOHEAD cohort, a prospective, pan-cancer collection of immunotherapy-naive patients receiving standard-of-care ICI treatment across the United States. Survival analyses were performed to evaluate associations between both individual and cumulative medication exposures and real-world overall survival (rwOS).

findingsOf 1,024 patients from the RADIOHEAD cohort, 55% (n = 564/1,024) were exposed to polypharmacy, defined as more than five drug classes, at ICI initiation. Polypharmacy, explored as a continuous variable of cumulative medication exposure, was significantly associated with worse rwOS (hazard ratio [HR] 1.06 [95% confidence interval [CI] 1.03-1.10], p < 0.001, q = 0.005). Among individual medication class exposures, there was a strong association between opioids and worse rwOS (HR 1.79 [95% CI 1.43-2.24], p < 0.001), as well as beta-blocker use (HR 1.38 [95% CI, 1.10-1.72], p = 0.005), after adjusting for clinically relevant covariates and patterns of co-prescription. The association between opioid exposure and worse rwOS was independent of additional palliative medication use (HR 1.61 [95% CI 1.09-2.36], p = 0.016, p for interaction = 0.4) and persisted in patients with early-stage and non-metastatic disease (p = 0.044).

conclusionsPolypharmacy and baseline medication exposures, particularly opioid and beta-blocker use, have prognostic significance for rwOS in patients with cancer receiving ICI treatment. This study evaluates the influence of baseline medications on ICI efficacy within the context of cumulative medication exposures reflective of co-prescription.

fundingThis study was supported in part by the National Institutes of Health and the Parker Institute for Cancer Immunotherapy (PICI).

Indexed as

Immune Checkpoint InhibitorsNeoplasmsPolypharmacyAdrenergic beta-AntagonistsAgedFemaleHumansMaleMiddle AgedProspective StudiesSurvival AnalysisUnited StatesAdrenergic beta-AntagonistsImmune Checkpoint Inhibitorsbaseline medicationsbeta-blockersco-prescriptionimmune checkpoint inhibitorsopioidsoverall survivalpan-cancerpolypharmacyreal-world cohortstandard-of-caretranslation to patients

Identifiers

PMID41999755
PMCPMC13152006

What Socratic 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 Socratic graph.