Evidence map›Paper›PMID 40344545›Full record

Trial reportJCO clinical cancer informatics2025

Assessing Algorithmic Fairness With a Multimodal Artificial Intelligence Model in Men of African and Non-African Origin on NRG Oncology Prostate Cancer Phase III Trials.

Mack Roach, Jingbin Zhang, Osama Mohamad, Douwe van der Wal, Jeffry P Simko, Sandy DeVries, Huei-Chung Huang, Songwan Joun, Edward M Schaeffer, Todd M Morgan and 18 more

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in JCO clinical cancer informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
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

28 authors.

Mack RoachUCSF Medical Center, San Francisco, CA.ORCID 0000-0002-3546-8565
Jingbin ZhangArtera, Santa Barbara, CA.
Osama MohamadUniversity of California San Francisco, San Francisco, CA.ORCID 0000-0003-2972-657X
Douwe van der WalArtera, Santa Barbara, CA.
Jeffry P SimkoUCSF Medical Center, San Francisco, CA.
Sandy DeVriesUCSF Medical Center, San Francisco, CA.
Huei-Chung HuangArtera, Santa Barbara, CA.
Songwan JounArtera, Santa Barbara, CA.
Edward M SchaefferNorthwestern University, Chicago, IL.
Todd M MorganUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, MI.ORCID 0000-0002-1140-0603
Jessica Keim-MalpassArtera, Santa Barbara, CA.ORCID 0000-0002-7035-8556
Emmalyn ChenArtera, Santa Barbara, CA.
Rikiya YamashitaArtera, Santa Barbara, CA.
Jedidiah M MonsonHematology-Oncology Medical Group of Fresno Inc, Fresno, CA.
Farah NazHorizon Health Network-Saint John Regional Hospital, Saint John, NB.
James WallaceIngalls Memorial Hospital, Harvey, IL.
Jean-Paul BaharyCHUM-Centre Hospitalier de l'Universite de Montreal, Montreal, QC.
Derek WilkeNova Scotia Cancer Centre/Nova Scotia Health/QEII Health Sciences Centre, Halifax, NS.ORCID 0000-0003-1803-5765
Sonny BatraVA Boston Healthcare System, Boston, MA.
Gregory B BiedermannUniversity of Missouri-Ellis Fischel, Columbia, MO.
Sergio FariaThe Research Institute of the McGill University Health Centre (MUHC), Montreal, QC.
Lindsay HwangKeck School of Medicine of USC, Los Angeles, CA.
Howard M SandlerCedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-8193-5769
Daniel E SprattUniversity Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland, OH.ORCID 0000-0002-5973-4741
Stephanie L PughNRG Oncology Statistics and Data Management Center, Philadelphia, PA.
Andre EstevaArtera, Santa Barbara, CA.
Phuoc T TranJohns Hopkins University/Sidney Kimmel Cancer Center, Baltimore, MD.ORCID 0000-0002-0147-0376
Felix Y FengUniversity of California San Francisco, San Francisco, CA.ORCID 0000-0002-0963-7687

Funding

NRG Oncology Network Group Operations Center - GY9 BIQSFP Reports/BudgetsU10CA180868 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI NORMAN WOLMARK · 2014 to 2026
$206.8M
Statistics CoreU10CA180822 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI James J. Dignam · 2014 to 2026
$146.4M
NRG Oncology NCORP Research Base-BIQSFPUG1CA189867 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Deborah Watkins Bruner, Lisa A. Kachnic · 2014 to 2026
$140.5M
NRG Oncology Biospecimen BankU24CA196067 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Tanner J. Freeman, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$42.6M
Resource Sharing CoreU54CA273956 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Luigi Marchionni · 2022 to 2026
$8.9M
UM LAPs -UG1 GrantUG1CA233160 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANNE F SCHOTT · 2019 to 2026
$5.4M
NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868NCI NIH HHS U24 CA196067NCI NIH HHS U54 CA273956NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA233160
6 · The paper itself

Abstract

purposeArtificial intelligence (AI) tools could improve clinical decision making or exacerbate inequities because of bias. African American (AA) men reportedly have a worse prognosis for prostate cancer (PCa) and are underrepresented in the development genomic biomarkers. We assess the generalizability of tools developed using a multimodal AI (MMAI) deep learning system using digital histopathology and clinical data from NRG/Radiation Therapy Oncology Group PCa trials across racial subgroups.

methodsIn total, 5,708 patients from five randomized phase III trials were included. Two MMAI algorithms were evaluated: (1) the distant metastasis (DM) MMAI model optimized to predict risk of DM, and (2) the PCa-specific mortality (PCSM) MMAI model optimized to focus on prediction death in the presence of DM (DDM). The prognostic performance of the MMAI algorithms was evaluated in AA and non-AA subgroups using time to DM (primary end point) and time to DDM (secondary end point). Exploratory end points included time to biochemical failure and overall survival with Fine-Gray or Cox proportional hazards models. Cumulative incidence estimates were computed for time-to-event end points and compared using Gray's test.

resultsThere were 948 (16.6%) AA patients, 4,731 non-AA patients (82.9%), and 29 (0.5%) patients with unknown or missing race status. The DM-MMAI algorithm showed a strong prognostic signal for DM in the AA (subdistribution hazard ratio [sHR], 1.2 [95% CI, 1.0 to 1.3];

conclusionUsing cooperative group data sets with a racially diverse population, the MMAI algorithm performed well across racial subgroups without evidence of algorithmic bias.

Indexed as

AlgorithmsArtificial IntelligenceProstatic NeoplasmsAgedBlack or African AmericanClinical Trials, Phase III as TopicHumansMaleMiddle AgedPrognosis

Identifiers

PMID40344545
PMCPMC12335010

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.