Evidence map›Paper›PMID 39746162›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Adjuvant Dose-Dense Chemotherapy in Hormone Receptor-Positive Breast Cancer.

Otto Metzger Filho, Karla Ballman, Jordan Campbell, Minetta Liu, Jennifer Ligibel, Mark Watson, Eveline Chen, Lili Du, Daniel Stover, Lisa Carey and 7 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 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. Trial
  2. Trial
  3. The Oncotype DX® 21-gene recurrence score and clinical outcomes in hormone receptor-positive, HER2-negative male breast cancer: a scoping review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  4. Article
  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

17 authors.

Otto Metzger FilhoDana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA.ORCID 0000-0003-0792-0320
Karla BallmanAlliance Statistics and Data Management Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-4492-0357
Jordan CampbellAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN.
Minetta LiuMayo Clinic, Rochester, MN.ORCID 0000-0002-8206-5232
Jennifer LigibelDana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA.ORCID 0000-0002-0633-3151
Mark WatsonWashington University School of Medicine, St Louis, MO.ORCID 0000-0002-3935-9980
Eveline ChenUniversity of Texas MD Anderson Cancer Center, Houston, TX.
Lili DuUniversity of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-0448-196X
Daniel StoverThe Ohio State University Wexner Medical Center, Columbus, OH.ORCID 0000-0001-9003-8165
Lisa CareyUniversity of North Carolina, Chapel Hill, NC.ORCID 0000-0003-2388-4649
Ann PartridgeDana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA.ORCID 0000-0002-4722-4824
Jeffrey KirshnerHematology/Oncology Associates of Central New York, East Syracuse, NY.
Hyman MussUniversity of North Carolina, Chapel Hill, NC.ORCID 0000-0003-2862-9970
Clifford HudisMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-7144-8791
Eric P WinerDana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA.ORCID 0000-0002-8819-1723
Larry NortonMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-3701-9250
W Fraser SymmansUniversity of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-1526-184X

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
Physician Scientist Training in Cancer ResearchT32CA009172 · NCI · DANA-FARBER CANCER INSTITUTE · PI Jennifer R Brown, James A. DeCaprio · 1985 to 2026
$17.1M
WASHINGTON UNIVERSITY / SITEMAN CANCER CENTER LEAD ACADEMIC SITEUG1CA233339 · NCI · WASHINGTON UNIVERSITY · PI NANCY L BARTLETT, Clifford Grant Robinson · 2019 to 2026
$11.3M
Network Lead Academic Participating Site: Memorial Sloan Kettering Cancer CenterUG1CA233290 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CAROL AGHAJANIAN, Darren Feldman · 2019 to 2026
$10.2M
OSU as a Network Lead Academic Participating Site for the NCI NCTNUG1CA233331 · NCI · OHIO STATE UNIVERSITY · PI John L. Hays, Dwight H. Owen · 2019 to 2026
$8.9M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
NCI, National Clinical Trials Network Lead Academic Participating Site (LAPS) UG1 (funded extension)UG1CA232760 · NCI · MAYO CLINIC ROCHESTER · PI Judy Caroline Boughey, Aaron Scott Mansfield · 2019 to 2026
$8.5M
UNC Lead Academic Participating SiteUG1CA233373 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A, DEES, ELIZABETH CLAIRE · 2019 to 2025
$3.5M
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009172NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233290NCI NIH HHS UG1 CA233331NCI NIH HHS UG1 CA233339NCI NIH HHS UG1 CA233373
6 · The paper itself

Abstract

purposeIn light of evolving evidence that some patients with node-positive estrogen receptor-positive (ER+) disease may receive less benefit from chemotherapy, this study reports 12-year outcomes of the C9741 trial overall, and by the sensitivity to endocrine therapy (SET2,3) test index, a biomarker measuring endocrine transcriptional activity, to identify patients most likely to benefit from dose-dense chemotherapy.

methodsIn all, 1,973 patients were randomly assigned to dose-dense versus conventional chemotherapy. Hazard ratios (HRs) for prognosis and for predictive interaction with chemotherapy schedule were estimated from Cox models of long-term disease-free survival (DFS) and overall survival (OS). SET2,3 was tested on the 682 banked RNA samples from ER+ cancers.

resultsDose-dense chemotherapy improved DFS in the overall study population by 23% (HR, 0.77 [95% CI, 0.66 to 0.90]) and OS by 20% (HR, 0.80 [95% CI, 0.67 to 0.95]); the benefits of dose-dense therapy were seen for ER+ and ER-negative subsets, without significant interaction between treatment arm and ER status. Low SET2,3 status was highly prognostic, but also predicted improved outcomes from dose-dense chemotherapy (interaction

conclusionAt 12-year follow-up, C9741 confirmed the sustained long-term benefit of adjuvant dose-dense chemotherapy for node-positive breast cancer. SET2,3 identified patients with ER+ breast cancer who benefited from dose-dense chemotherapy, and specifically, this benefit was predicted by low endocrine activity in the cancer, rather than tumor burden, molecular subtype, or menopausal status.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsReceptors, EstrogenAdultAgedBiomarkers, TumorChemotherapy, AdjuvantDisease-Free SurvivalFemaleHumansMiddle AgedProportional Hazards ModelsBiomarkers, TumorReceptors, Estrogen

Identifiers

PMID39746162
PMCPMC11954676

What OpenQuestion 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 OpenQuestion graph.