Evidence map›Paper›PMID 39854806›Full record

Trial reportGynecologic oncology2025

Molecular classification of endometrial cancers (EC) and association with relapse-free survival (RFS) and overall survival (OS) outcomes: Ancillary analysis of GOG-0258.

Aine Clements, Danielle Enserro, Kyle C Strickland, Rebecca Previs, Daniela Matei, David Mutch, Matthew Powell, Ann Klopp, David Scott Miller, William Small and 13 more

Registry-linked trialAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Gynecologic oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00942357 (A Randomized Phase III Trial of Cisplatin and Tumor Volume Directed Irradiation Followed by Carboplatin and Paclitaxel vs. Carboplatin and Paclitaxel for Optimally Debulked, Advanced Endometrial Carcinoma), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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.

NCT00942357 phase3unknown statusnot on this map

A Randomized Phase III Trial of Cisplatin and Tumor Volume Directed Irradiation Followed by Carboplatin and Paclitaxel vs. Carboplatin and Paclitaxel for Optimally Debulked, Advanced Endometrial Carcinoma

TypeinterventionalSponsorGynecologic Oncology GroupRan2009 to 2024Enrolled813ConditionsEndometrial Clear Cell Adenocarcinoma, Endometrial Serous Adenocarcinoma, Stage IA Uterine Corpus Cancer AJCC v7, Stage IB Uterine Corpus Cancer AJCC v7ArmsCarboplatin, Cisplatin, Internal Radiation Therapy, Paclitaxel, Quality-of-Life Assessment
3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Reply to: Comment on The Study of NRG258: Limitations and Future Directions.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Article
  8. Updates and controversies in the management of uterine serous carcinoma and uterine carcinosarcoma.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2025
    Review
  9. Review
  10. Review
  11. Review
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

23 authors.

Aine ClementsOhioHealth, Columbus, OH, United States of America. Electronic address: Aine.Clements@ohiohealth.com.
Danielle EnserroRoswell Park, Clinical Trials Development, Buffalo, NY, United States of America. Electronic address: enserrod@nrgoncology.org.
Kyle C StricklandDuke University, Durham, NC, United States of America. Electronic address: kyle.strickland@duke.edu.
Rebecca PrevisLabcorp, Medical Affairs, Chapel Hill, NC, United States of America. Electronic address: Rebeccaann.previs@labcorp.com.
Daniela MateiFeinberg School of Medicine, Northwestern, Chicago, IL, United States of America. Electronic address: daniela.matei@northwestern.edu.
David MutchWashington University in St Louis, St Louis, MO, United States of America. Electronic address: mutchd@wustl.edu.
Matthew PowellWashington University in St Louis, St Louis, MO, United States of America. Electronic address: mpowell@wustl.edu.
Ann KloppMD Anderson Cancer Center, Houston, TX, United States of America. Electronic address: aklopp@mdanderson.org.
David Scott MillerUniversity of Texas Southwestern Medical Center, Dallas, TX, United States of America. Electronic address: David.miller@utsouthwestern.edu.
William SmallLoyola Medicine, Maywood, IL, United States of America. Electronic address: wmsmall@lumc.edu.
Paul DiSilvestroWomen and Infants, Providence, RI, United States of America. Electronic address: PDiSilvestro@Wihri.org.
Nick SpirtosWomen's Cancer Center of Nevada, Las Vegas, NV, United States of America. Electronic address: nmspirtos@wccenter.com.
Casey CosgroveThe Ohio State University, Columbus, OH, United States of America. Electronic address: Casey.Cosgrove@osumc.edu.
Greg SfakianosPiedmont Columbus Midtown JBACC Medical Oncology, Columbus, GA, United States of America. Electronic address: Gregory.Sfakianos@piedmont.org.
J Rebecca LiuCancer Research Consortium of Michigan, Ann Arbor, MI, United States of America. Electronic address: rliu@umich.edu.
Roberto VargasThe Cleveland Clinic, Cleveland, OH, United States of America. Electronic address: VARGASR@ccf.org.
Mark ShahinHanjani Institute for Gynecologic Oncology Abington Memorial Hospital, Abington, PA, United States of America. Electronic address: Mark.Shahin@jefferson.edu.
Bradley CorrUniversity of Colorado School of Medicine, Aurora, CO, United States of America. Electronic address: bradley.corr@cuanschutz.edu.
Kimberly DessourcesUniversity of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America. Electronic address: Kimberly_Dessources@med.unc.edu.
Frederick UelandUniversity of Kentucky Markey Cancer Center, Lexington, KY, United States of America. Electronic address: Frederick.Ueland@uky.edu.
David WarshalCooper Hospital University Medical Center, Camden, NJ, United States of America. Electronic address: Warshal-David@CooperHealth.edu.
Jessica GillenCancer Research for the Ozarks, Springfield, MO, United States of America. Electronic address: Jessica.gillen@coxhealth.com.
Angeles Alvarez SecordDuke University, Durham, NC, United States of America. Electronic address: angeles.secord@duke.edu.

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
Route 66 Endometrial Cancer SPOREP50CA265793 · NCI · WASHINGTON UNIVERSITY · PI Esther Jiaxin Lu · 2023 to 2026
$11.6M
WASHINGTON UNIVERSITY / SITEMAN CANCER CENTER LEAD ACADEMIC SITEUG1CA233339 · NCI · WASHINGTON UNIVERSITY · PI NANCY L BARTLETT, Clifford Grant Robinson · 2019 to 2026
$11.3M
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
NCI NIH HHS P50 CA265793NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA233331NCI NIH HHS UG1 CA233339
6 · The paper itself

Abstract

purposeDetermine if molecular classification using mismatch repair (MMR) and p53 protein expression predicts recurrence-free survival (RFS) and overall survival (OS) in endometrial cancer (EC) patients treated with chemotherapy and radiation (CRT) versus chemotherapy (CT).

methodsGOG-0258, a phase III randomized trial (NCT00942357), compared CRT to CT. Immunohistochemistry assessed MMR and p53 status. Kaplan-Meier curves and adjusted Cox models analyzed survival outcomes by molecular subtype.

resultsECs classified as deficient MMR (dMMR) (27 %), p53 abnormal (p53abn) (24 %), and p53 wild type (p53wt) (49 %). p53abn were more frequent in patients that were older, Black, and had serous histology (p < 0.001). Median follow up was 113 months. Five-year RFS and OS were worse with p53abn (29 % [Hazard Ratio (HR) = 3.39 (95 % Confidence Interval (CI): 2.34-4.91)] and 39 % [HR = 4.64 (95 % CI: 3.16-6.79)] compared to those with p53wt (referent) (p < 0.001). The five-year RFS and OS for dMMR cancers were (58 % [HR = 1.30 (95 % CI: 0.85-1.97)] and 77 % [HR = 1.53 (95 % CI: 0.99-2.36)] compared to those with p53wt (69 % and 85 %). After adjusting for age, gross residual disease, and treatment, p53wt improved RFS with CRT compared to CT in an exploratory analysis (77 % vs 60 %; HR = 0.54 (95 % CI: 0.32-0.94). The 5-year and 10-year OS rates were similar in CRT compared to CT in all subgroups.

conclusionMolecular classification appears to be predictive and prognostic, with worse survival in those with p53abn tumors. In an exploratory analysis, p53wt appears to predict improved RFS, favoring CRT over CT. There was no difference in treatment efficacy based on molecular subtype for OS.

Indexed as

Endometrial NeoplasmsTumor Suppressor Protein p53AdultAgedChemoradiotherapyDisease-Free SurvivalDNA Mismatch RepairFemaleHumansMiddle AgedTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID39854806
PMCPMC11929956

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Registered trials

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.