Evidence map›Paper›PMID 37418832›Full record

Trial reportGynecologic oncology2023

A phase 2 study of dasatinib in recurrent clear cell carcinoma of the ovary, fallopian tube, peritoneum or endometrium: NRG oncology/gynecologic oncology group study 0283.

Roisin E O'Cearbhaill, Austin Miller, Robert A Soslow, Heather A Lankes, Deborah DeLair, Sheila Segura, Shweta Chavan, Dmitriy Zamarin, Robert DeBernardo, Kathleen Moore and 5 more

Open access · greenAbstract readClinical Trial, Phase II
In one paragraph

Trial report 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
0.6field-weighted citation impact, top 30% 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, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  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

15 authors at 11 institutions in 1 country.

Roisin E O'CearbhaillMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: ocearbhr@mskcc.org.
Austin MillerRoswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: millera@nrgoncology.org.
Robert A SoslowMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: soslowr@mskcc.org.
Heather A LankesNRG Oncology, Operations Center-Philadelphia East, Philadelphia, PA, United States of America; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH, United States of America. Electronic address: lankesh@nrgoncology.org.
Deborah DeLairNorthwell Health, Greenvale, New York, NY, United States of America. Electronic address: ddelair@northwell.edu.
Sheila SeguraIndiana University School of Medicine, Indianapolis, IN, United States of America. Electronic address: ssegura@iu.edu.
Shweta ChavanMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: schavan@repertoire.com.
Dmitriy ZamarinMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: zamarind@mskcc.org.
Robert DeBernardoCase Western University, Cleveland, OH, United States of America. Electronic address: DEBERNR@ccf.org.
Kathleen MooreUniversity of Oklahoma, Oklahoma City, OK, United States of America. Electronic address: Kathleen-Moore@ouhsc.edu.
John MoroneyUniversity of Chicago, Chicago, IL, United States of America. Electronic address: jwmoroney@bsd.uchicago.edu.
Mark ShahinAbington Memorial Hospital, Willow Grove, PA, United States of America. Electronic address: Mark.Shahin@jefferson.edu.
Premal H ThakerWashington University, St. Louis, MO, United States of America. Electronic address: thakerp@wudosis.wustl.edu.
Andrea E Wahner-HendricksonMayo Clinic, Rochester, MN, United States of America. Electronic address: WahnerHendrickson.Andrea@mayo.edu.
Carol AghajanianMemorial Sloan Kettering Cancer Center, New York, NY, United States of America. Electronic address: aghajanc@mskcc.org.
Memorial Sloan Kettering Cancer Center · USAbington Memorial Hospital · USIndiana University – Purdue University Indianapolis · USMayo Clinic in Florida · USNorthwell Health · USNRG Oncology · USRoswell Park Comprehensive Cancer Center · USUniversity of Chicago · USUniversity of Oklahoma · USWashington University in St. Louis · USWestern University of Health Sciences · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 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 James J. Dignam · 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
NRG Oncology Biospecimen BankU24CA196067 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Tanner J. Freeman, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$42.6M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI SCOTT H KAUFMANN · 2009 to 2026
$37.0M
University of Buffalo Clinical and Translational Science Institute - Supplement SchulyerUL1TR001412 · NCATS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MURPHY, TIMOTHY F · 2015 to 2024
$33.8M
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
Network Lead Academic Participating Site Grant from the Roswell Park Cancer InstituteUG1CA233191 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI LELE, SHASHIKANT, LEVINE, ELLIS G · 2019 to 2025
$3.1M
NCATS NIH HHS UL1 TR001412NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA136393NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868NCI NIH HHS U24 CA196067NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA233191NCI NIH HHS UG1 CA233290NCI NIH HHS UG1 CA233339
6 · The paper itself

Abstract

objectiveGynecologic cancers are traditionally managed according to their presumed site of origin, without regard to the underlying histologic subtype. Clear cell histology is associated with chemotherapy refractoriness and poor survival. Mutations in SWI/SNF chromatin remodeling complex member ARID1A, which encodes for BAF250a protein, are common in clear cell and endometriosis-associated endometrioid carcinomas. High-throughput cell-based drug screening predicted activity of dasatinib, a tyrosine kinase inhibitor, in ARID1A-mutant clear cell carcinoma.

methodsWe conducted a phase 2 clinical trial of dasatinib 140 mg once daily by mouth in patients with recurrent or persistent ovarian and endometrial clear cell carcinoma. Patients with measurable disease were enrolled and then assigned to biomarker-defined populations based on BAF250a immunohistochemistry. The translational endpoints included broad next-generation sequencing to assess concordance of protein expression and treatment outcomes.

resultsTwenty-eight patients, 15 of whom had tumors with retained BAF250a and 13 with loss of BAF250a were evaluable for treatment response and safety. The most common grade 3 adverse events were anemia, fatigue, dyspnea, hyponatremia, pleural effusion, and vomiting. One patient had a partial response, eight (28%) had stable disease, and 15 (53.6%) had disease progression. Twenty-three patients had next-generation sequencing results; 13 had a pathogenic ARID1A alteration. PIK3CA mutations were more prevalent in ARID1A-mutant tumors, while TP53 mutations were more prevalent in ARID1A wild-type tumors.

conclusionsDasatinib was not an effective single-agent treatment for recurrent or persistent ovarian and endometrial clear cell carcinoma. Studies are urgently needed for this rare gynecologic subtype.

Indexed as

Adenocarcinoma, Clear CellCarcinoma, EndometrioidOvarian NeoplasmsDasatinibEndometriumFallopian TubesFemaleHumansPeritoneumDasatinibARID1A mutationBAF250aClear cell cancerDasatinibOvarian cancer

Identifiers

PMID37418832
PMCPMC10529107
OpenAlexW4383222157

What Socratic 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 Socratic graph.