Evidence map›Paper›PMID 42842849›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2026

NRG-BR002: A Randomized Phase II/III Trial of Metastasis-Directed Ablation With First-Line Systemic Therapy for Oligometastatic Breast Cancer.

Steven J Chmura, Kathryn A Winter, Wendy A Woodward, Virginia F Borges, Joseph K Salama, Hania A Al-Hallaq, Martha M Matuszak, Michael T Milano, Nora T Jaskowiak, Reshma Jagsi and 20 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 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

30 authors.

Steven J ChmuraMD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-8851-7108
Kathryn A WinterNRG Oncology Statistics and Data Management Center, Philadelphia, PA.
Wendy A WoodwardMD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-7935-739X
Virginia F BorgesUniversity of Colorado Hospital, Aurora, CO.ORCID 0000-0003-1158-7524
Joseph K SalamaDuke University Medical Center, Durham, NC.ORCID 0000-0001-5159-4687
Hania A Al-HallaqEmory University Hospital/Winship Cancer Institute, Atlanta, GA.ORCID 0000-0003-4274-6524
Martha M MatuszakUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, MI.
Michael T MilanoUniversity of Rochester, Rochester, NY.ORCID 0000-0001-8676-2855
Nora T JaskowiakUniversity of Chicago Comprehensive Cancer Center, Chicago, IL.
Reshma JagsiEmory University Hospital/Winship Cancer Institute, Atlanta, GA.ORCID 0000-0001-6562-1228
Peter KuhnUniversity of Southern California, Michelson Convergent Science Institute in Cancer, Los Angeles, CA.ORCID 0000-0003-2629-4505
Anthony LucciMD Anderson Cancer Center, Houston, TX.
Salyna MeasMD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-5588-6337
Stephanie N ShishidoUniversity of Southern California, Los Angeles, CA.
Jeremy MasonUniversity of Southern California, Los Angeles, CA.ORCID 0000-0002-5933-5003
Jose G BazanOhio State University Comprehensive Cancer Center, Columbus, OH.
Robert A NordalTom Baker Cancer Centre, Calgary, AB.
David Y LeeUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, NM.
Benjamin D SmithMD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-7866-1093
Zsolt GabosCross Cancer Institute, University of Alberta, Edmonton, Canada.ORCID 0000-0002-7198-1876
Jason C YeKeck School of Medicine of the University of Southern California, Los Angeles, CA.ORCID 0000-0001-9087-6011
Shannon T KahnPiedmont Healthcare, Atlanta, GA.
Laura A VallowMayo Clinic, Jacksonville, FL.
Imran ZoberiWashington University School of Medicine, Saint Louis, MO.
Wajeeha RazaqUniversity of Oklahoma Health Sciences Center, Oklahoma City, OK.
Mark V MishraUniversity of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0002-2588-1575
Kristin M LupinacciUniversity of Pittsburgh School of Medicine, Pittsburg, PA.ORCID 0000-0002-3779-9878
Jennifer MoughanNRG Oncology Statistics and Data Management Center, Philadelphia, PA.
Eleftherios P MamounasOrlando Health Cancer Institute, Orlando, FL.ORCID 0000-0002-9476-2553
Julia R WhiteUniversity of Kansas Cancer Center, Kansas City, KS.ORCID 0000-0001-6624-5631

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, GREG YOTHERS · 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
IROC: Enhancing local enrolling site radiological data capture capabilities for NCTN trialsU24CA180803 · NCI · AMERICAN COLLEGE OF RADIOLOGY · PI Thomas J. FitzGerald, MICHAEL V KNOPP · 2014 to 2026
$116.2M
UG1 - NCTN (Network Lead)UG1CA233327 · NCI · UNIVERSITY OF CHICAGO · PI STEVEN J CHMURA, HEDY L KINDLER · 2019 to 2026
$4.4M
Multi-modal Liquid Biopsy Early Assessment of Breast Cancer, Pancreatic Cancer, and Multiple MyelomaU01CA285013 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KUHN, PETER · 2023 to 2025
$3.4M
NCI National Clinical Trials Network-Network Lead Academic Participating SitesU10CA180836 · NCI · UNIVERSITY OF CHICAGO · PI CHMURA, STEVEN J, KINDLER, HEDY L · 2014 to 2018
$3.2M
NCI NIH HHS U01 CA285013NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180836NCI NIH HHS U10 CA180868NCI NIH HHS U24 CA180803NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA233327
6 · The paper itself

Abstract

purposeMetastasis-directed therapy is increasingly used for oligometastatic breast cancer, despite its uncertain benefit during first-line systemic therapy. We evaluated whether metastasis-directed ablation improves progression-free survival (PFS) compared with first-line systemic therapy alone in patients with oligometastatic breast cancer.

methodsNRG-BR002 is a randomized phase II/III trial across US/Canadian institutions. Participants had ≤4 metastases, controlled primary disease, ≤12 months of first-line systemic therapy without progression with all visible metastases amenable to stereotactic body radiation therapy (SBRT) or surgical resection and were randomly assigned 1:1 to systemic therapy alone (no ablation) or with metastasis-directed ablation (ablation). The primary end point was PFS, defined as time to progression or death. Secondary end points included overall survival (OS) and toxicity. Circulating tumor cells (CTCs) were evaluated as exploratory biomarkers.

resultsFrom December 2014 to September 2019, 129 patients were enrolled; 125 were eligible for analysis. Median age was 54 years; 79% had hormone receptor-positive, human epidermal growth factor receptor 2‑negative disease, 60% solitary metastasis, 50% bone involvement, and 37% bone only. Ablation was delivered via SBRT for 93%. With 72 PFS events and a median follow-up of 29.9 months, median PFS was 23.0 months (no ablation) versus 19.5 months (ablation; hazard ratio [HR], 0.92 [70% CI, 0.71 to 1.17; 95% CI, 0.57 to 1.47]; one-sided

conclusionThe addition of metastasis-directed ablation added to first-line systemic therapy did not improve PFS or OS in patients with oligometastatic breast cancer. Ablation should not be routinely used outside of clinical trials, except for palliation.

Identifiers

PMID42842849
PMCPMC13647293

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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 OpenQuestion graph.