Evidence map›Paper›PMID 37634258›Full record

ArticleGynecologic oncology2023

Mixed clear cell/endometrioid and clear cell/serous carcinoma of the uterus are clinicopathologically similar to pure clear cell carcinoma: An NRG Oncology/Gynecologic Oncology Group (GOG-210) study of 311 women.

Ian S Hagemann, Wei Deng, Richard J Zaino, Matthew A Powell, Camille Gunderson Jackson, Casey Cosgrove, Cara Mathews, Michael L Pearl, Steven Waggoner, Rahel Ghebre and 9 more

Open access · greenAbstract read
In one paragraph

Article in Gynecologic oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

19 authors at 16 institutions in 2 countries.

Ian S HagemannWashington University School of Medicine, St. Louis, MO, United States of America. Electronic address: hagemani@wustl.edu.
Wei DengNRG Oncology, Clinical Trial Development Division; Biostatistics & Bioinformatics: Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: dengw@nrgoncology.org.
Richard J ZainoPennsylvania State University, Hershey, PA, United States of America. Electronic address: rzaino@psu.edu.
Matthew A PowellWashington University School of Medicine, St. Louis, MO, United States of America. Electronic address: mpowell@wustl.edu.
Camille Gunderson JacksonUniversity of Oklahoma Health Sciences Center and Stephenson Cancer Center, Oklahoma City, OK, United States of America. Electronic address: camille.jackson@mercy.net.
Casey CosgroveOhio State University Comprehensive Cancer Center, Columbus, OH, United States of America. Electronic address: casey.cosgrove@osumc.edu.
Cara MathewsWomen & Infants Hospital, Providence, RI, United States of America. Electronic address: cmathews@wihri.org.
Michael L PearlStony Brook University Medical Center, Stony Brook, NY, United States of America. Electronic address: michael.pearl@sbumed.org.
Steven WaggonerCleveland Clinic, Cleveland, OH, United States of America. Electronic address: waggons@ccf.org.
Rahel GhebreMasonic Cancer Center, University of Minnesota, Minneapolis, MN, United States of America. Electronic address: ghebr004@umn.edu.
Shashikant LeleRoswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: shashi.lele@roswellpark.org.
Saketh GuntupalliUniversity of Colorado Cancer Center, Aurora, CO, United States of America. Electronic address: saketh.guntupalli@ucdenver.edu.
Angeles Alvarez SecordDuke University Medical Center, Durham, NC, United States of America. Electronic address: angeles.secord@duke.edu.
Olga IoffeUniversity of Maryland School of Medicine, Baltimore, MD, United States of America. Electronic address: oioffe@fpi.umaryland.edu.
Golnar RastyUniversity of Toronto, Markham, Ontario, Canada. Electronic address: grasty@oakvalleyhealth.ca.
Meenakshi SinghStony Brook University Medical Center, Stony Brook, NY, United States of America.
Robert SoslowMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: soslowr@mskcc.org.
William CreasmanMedical University of South Carolina Medical Center, Charleston, SC, United States of America. Electronic address: creasman@musc.edu.
David G MutchWashington University School of Medicine, St. Louis, MO, United States of America. Electronic address: mutchd@wustl.edu.
Washington University in St. Louis · USStony Brook University Hospital · USCleveland Clinic · USDuke Medical Center · USMedical University of South Carolina · USMemorial Sloan Kettering Cancer Center · USNRG Oncology · USPennsylvania State University · USProvidence College · USRoswell Park Comprehensive Cancer Center · USThe Ohio State University · USUniversity of Colorado Cancer Center · USUniversity of Maryland, Baltimore · USUniversity of Minnesota · USUniversity of Oklahoma Health Sciences Center · USUniversity of Toronto · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
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 Mei-Yin C Polley · 2014 to 2026
$146.4M
NRG Oncology Biospecimen BankU24CA196067 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Tanner J. Freeman, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$42.6M
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
NCI NIH HHS P30 CA008748NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868NCI NIH HHS U24 CA196067NCI NIH HHS UG1 CA233290
6 · The paper itself

Abstract

objectivesClear cell carcinoma is a high-risk subtype of endometrial cancer. Some patients have a mixture of clear cell carcinoma with other histologic types (endometrioid or serous) or cannot be neatly assigned to one of these types. Protocol GOG-8032 within GOG-210 was designed to determine whether these tumors differ from pure clear cell carcinoma in stage at diagnosis, initial pattern of spread, or patient survival.

methodsThe term "mixed" was applied to tumors with multiple identifiable components, and "indeterminate" was applied to tumors with features intermediate between different histologic types. Three hundred eleven women with pure, mixed, or indeterminate clear cell carcinoma were identified in a larger cohort of patients undergoing hysterectomy for endometrial cancer in GOG-210. Histologic slides were centrally reviewed by expert pathologists. Baseline and follow-up data were analyzed.

resultsOne hundred thirty-six patients had pure clear cell carcinoma and 175 had a mixed or indeterminate clear cell pattern. Baseline clinicopathologic characteristics were similar except for a small difference in age at presentation. Univariate survival analysis confirmed the significance of typical endometrial cancer prognostic factors. Patients in the mixed categories had disease-free and overall survival similar to pure clear cell carcinoma, but the indeterminate clear cell/endometrioid group had longer survival.

conclusionIn clear cell endometrial cancer, the presence of a definite admixed endometrioid or serous component did not correlate with a significant difference in prognosis. Patients whose tumors had indeterminate clear cell features had better prognosis. Some of these tumors may be endometrioid tumors mimicking clear cell carcinoma.

Indexed as

Adenocarcinoma, Clear CellCarcinoma, EndometrioidEndometrial NeoplasmsFemaleHumansNeoplasm StagingPrognosisUterusClear cell carcinomaClinical trialsEndometrial carcinomaGynecologic oncologyMalignant mixed tumorsPathologySurvival analysis

Identifiers

PMID37634258
PMCPMC10806844
OpenAlexW4386175036

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.