Evidence map›Paper›PMID 34964855›Full record

SynthesisJAMA network open2021

Comparison of Response to Definitive Radiotherapy for Localized Prostate Cancer in Black and White Men: A Meta-analysis.

Ting Martin Ma, Tahmineh Romero, Nicholas G Nickols, Matthew B Rettig, Isla P Garraway, Mack Roach, Jeff M Michalski, Thomas M Pisansky, W Robert Lee, Christopher U Jones and 21 more

Open access · goldAbstract readComparative StudyMeta-Analysis
In one paragraph

Synthesis in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
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  4. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 17 institutions in 1 country.

Ting Martin MaDepartment of Radiation Oncology, University of California, Los Angeles (UCLA).
Tahmineh RomeroStatistics Core, David Geffen School of Medicine, UCLA.
Nicholas G NickolsDepartment of Radiation Oncology, University of California, Los Angeles (UCLA).
Matthew B RettigDivision of Hematology and Oncology, David Geffen School of Medicine, UCLA.
Isla P GarrawayDepartment of Urology, UCLA.
Mack RoachDepartment of Radiation Oncology, Helen Diller Comprehensive Cancer Center, University of California, San Francisco.
Jeff M MichalskiWashington University School of Medicine in St Louis, St Louis, Missouri.
Thomas M PisanskyDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
W Robert LeeDepartment of Radiation Oncology, Duke University School of Medicine, Durham, North Carolina.
Christopher U JonesSutter Medical Group and Sutter Cancer Centers, Roseville, California.
Seth A RosenthalSutter Medical Group and Sutter Cancer Centers, Roseville, California.
Chenyang WangDepartment of Radiation Oncology, Division of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston.
Holly HartmanDepartment of Radiation Oncology, University of Michigan, Ann Arbor.
Paul L NguyenDepartment of Radiation Oncology, Brigham and Women's Hospital/Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Felix Y FengDepartment of Radiation Oncology, Helen Diller Comprehensive Cancer Center, University of California, San Francisco.
Paul C BoutrosDepartment of Urology, UCLA.
Christopher SaigalDepartment of Urology, UCLA.
Karim ChamieDepartment of Urology, UCLA.
William C JacksonDepartment of Radiation Oncology, University of Michigan, Ann Arbor.
Todd M MorganDepartment of Urology, University of Michigan, Ann Arbor.
Rohit MehraDepartment of Pathology, University of Michigan, Ann Arbor.
Simpa S SalamiDepartment of Urology, University of Michigan, Ann Arbor.
Randy VinceDepartment of Urology, University of Michigan, Ann Arbor.
Edward M SchaefferDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Brandon A MahalDepartment of Radiation Oncology, Brigham and Women's Hospital/Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Robert T DessDepartment of Radiation Oncology, University of Michigan, Ann Arbor.
Michael L SteinbergDepartment of Radiation Oncology, University of California, Los Angeles (UCLA).
David ElashoffStatistics Core, David Geffen School of Medicine, UCLA.
Howard M SandlerDepartment of Radiation Oncology, Cedars-Sinai Medical Center, Los Angeles, California.
Daniel E SprattDepartment of Radiation Oncology, University Hospitals Seidman Cancer Center, Cleveland Medical Center, Cleveland, Ohio.
Amar U KishanDepartment of Radiation Oncology, University of California, Los Angeles (UCLA).
University of Michigan–Ann Arbor · USUCLA Health · USVA Greater Los Angeles Healthcare System · USSutter Roseville Medical Center · USUniversity of California, Los Angeles · USCedars-Sinai Medical Center · USDana-Farber Cancer Institute · USDuke University · USHarvard University · USMayo Clinic · USNorthwestern University · USThe University of Texas MD Anderson Cancer Center · USUCLA Jonsson Comprehensive Cancer CenterUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity Hospitals Seidman Cancer Center · USUniversity of California, San Francisco · USWashington University in St. Louis · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Robert Damoiseaux · 1985 to 2026
$134.5M
UCLA SPORE IN PROSTATE CANCERP50CA092131 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REITER, ROBERT E · 2002 to 2023
$42.6M
NCI NIH HHS P30 CA016042NCI NIH HHS P50 CA092131
6 · The paper itself

Abstract

Importance: Black men have a 2-fold increased risk of dying from prostate cancer compared with White men. However, race-specific differences in response to initial treatment remain unknown. Objective: To compare overall and treatment-specific outcomes of Black and White men with localized prostate cancer receiving definitive radiotherapy (RT). Data Sources: A systematic search was performed of relevant published randomized clinical trials conducted by the NRG Oncology/Radiation Therapy Oncology Group between January 1, 1990, and December 31, 2010. This meta-analysis was performed from July 1, 2019, to July 1, 2021. Study Selection: Randomized clinical trials of definitive RT for patients with localized prostate cancer comprising a substantial number of Black men (self-identified race) enrolled that reported on treatment-specific and overall outcomes. Data Extraction and Synthesis: Individual patient data were obtained from 7 NRG Oncology/Radiation Therapy Oncology Group randomized clinical trials evaluating definitive RT with or without short- or long-term androgen deprivation therapy. Unadjusted Fine-Gray competing risk models, with death as a competing risk, were developed to evaluate the cumulative incidences of end points. Cox proportional hazards models were used to evaluate differences in all-cause mortality and the composite outcome of distant metastasis (DM) or death. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline was followed. Main Outcomes and Measures: Subdistribution hazard ratios (sHRs) of biochemical recurrence (BCR), DM, and prostate cancer-specific mortality (PCSM). Results: A total of 8814 patients (1630 [18.5%] Black and 7184 [81.5%] White) were included; mean (SD) age was 69.1 (6.8) years. Median follow-up was 10.6 (IQR, 8.0-17.8) years for surviving patients. At enrollment, Black men were more likely to have high-risk disease features. However, even without adjustment, Black men were less likely to experience BCR (sHR, 0.88; 95% CI, 0.58-0.91), DM (sHR, 0.72; 95% CI, 0.58-0.91), or PCSM (sHR, 0.72; 95% CI, 0.54-0.97). No significant differences in all-cause mortality were identified (HR, 0.99; 95% CI, 0.92-1.07). Upon adjustment, Black race remained significantly associated with improved BCR (adjusted sHR, 0.79; 95% CI, 0.72-0.88; P < .001), DM (adjusted sHR, 0.69; 95% CI, 0.55-0.87; P = .002), and PCSM (adjusted sHR, 0.68; 95% CI, 0.50-0.93; P = .01). Conclusions and Relevance: The findings of this meta-analysis suggest that Black men enrolled in randomized clinical trials present with more aggressive disease but have better BCR, DM, and PCSM with definitive RT compared with White men, suggesting that other determinants of outcome, such as access to care, are important factors of achieving racial equity.

Indexed as

Black PeopleHumansMaleProstatic NeoplasmsRandomized Controlled Trials as TopicTreatment OutcomeWhite People

Identifiers

PMID34964855
PMCPMC8717118
OpenAlexW4200518484

What OpenQuestion holds

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LicenceCC BY
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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.