Evidence map›Paper›PMID 30135020›Full record

Trial reportGynecologic oncology2018

Does adjuvant chemotherapy dose modification have an impact on the outcome of patients diagnosed with advanced stage ovarian cancer? An NRG Oncology/Gynecologic Oncology Group study.

Alexander B Olawaiye, James J Java, Thomas C Krivak, Michael Friedlander, David G Mutch, Gretchen Glaser, Melissa Geller, David M O'Malley, Robert M Wenham, Roger B Lee and 3 more

Erratum issuedOpen access · greenAbstract readClinical Trial, Phase IIIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Gynecologic oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Article
  3. Surgery in ovarian cancer patients older than 70 years of age and frailty assessment.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  4. Article
  5. Article
  6. Framework to leverage physical therapists for the assessment and treatment of chemotherapy-induced peripheral neurotoxicity (CIPN).Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 13 institutions in 2 countries.

Alexander B OlawaiyeDivision of Gynecologic Oncology, Magee-Womens Hospital of UPMC, Pittsburgh, PA, United States of America. Electronic address: olawaiyea@mail.magee.edu.
James J JavaNRG Oncology, Clinical Trial Development Division, Biostatistics & Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263, United States of America.
Thomas C KrivakDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Western Pennsylvania Hospital, Pittsburgh, PA, United States of America. Electronic address: thomas.krivak@ahn.org.
Michael FriedlanderPrince of Wales Clinical School UNSW, Department of Medical Oncology, The Prince of Wales Hospital, Sydney, Australia. Electronic address: michael.friedlander@sesiahs.health.nsw.gov.au.
David G MutchDept. of Obstetrics and Gynecology, Washington University School of Medicine, Saint Louis, MO 63110, United States of America. Electronic address: mutchd@wudosis.wustl.edu.
Gretchen GlaserGynecologic Oncology, Carilion Clinic Gynecological Oncology, Roanoke, VA 24016, United States of America. Electronic address: geglaser@carilionclinic.org.
Melissa GellerDept. of Obstetrics, Gynecology and Women's Health, University of Minnesota Medical Center-Fairview, Minneapolis, MN 55455, United States of America. Electronic address: gelle005@umn.edu.
David M O'MalleyDept. of Obstetrics and Gynecology, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, United States of America. Electronic address: omalley.46@osu.edu.
Robert M WenhamDepartment of Gynecologic Oncology, Moffitt Cancer Center and Research Institute, Tampa, FL 33612, United States of America. Electronic address: robert.wenham@moffitt.org.
Roger B LeeTacoma General Hospital, Tacoma, WA, United States of America.
Diane C BodurkaDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States of America. Electronic address: dcbodurka@mdanderson.org.
Thomas J HerzogDept. of Obstetrics & Gynecology, University of Cincinnati Cancer Institute, University of Cincinnati, Cincinnati, OH 45267, United States of America. Electronic address: herzogtj@ucmail.uc.edu.
Michael A BookmanThe Permanente Medical Group, Inc. 2350 Geary Blvd, Room 115 San Francisco, CA 94115, United States of America. Electronic address: michael.bookman@usoncology.com.
Carilion Clinic · USColorado Permanente Medical Group · USFairview Health Services · USMagee-Womens Hospital · USMoffitt Cancer Center · USMultiCare Tacoma General Hospital · USPrince of Wales Hospital · AURoswell Park Comprehensive Cancer Center · USThe Ohio State University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Cincinnati · USWashington University in St. Louis · USWestern Pennsylvania Hospital · US

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
GYNECOLOGIC ONCOLOGY GROUP HEADQUARTERSU10CA027469 · NCI · GYNECOLOGIC ONCOLOGY GROUP · PI DISAIA, PHILIP J. · 1985 to 2013
$132.6M
GYNECOLOGIC ONCOLOGY GROUP STATISTICAL OFFICEU10CA037517 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI BLESSING, JOHN A · 1985 to 2013
$67.4M
NCI NIH HHS U10 CA027469NCI NIH HHS U10 CA037517NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868
6 · The paper itself

Abstract

purposeTo determine the relationship between chemotherapy dose modification (dose adjustment or treatment delay), overall survival (OS) and progression-free survival (PFS) for women with advanced-stage epithelial ovarian carcinoma (EOC) and primary peritoneal carcinoma (PPC) who receive carboplatin and paclitaxel.

methodsWomen with stages III and IV EOC and PPC treated on the Gynecologic Oncology Group phase III trial, protocol 182, who completed eight cycles of carboplatin with paclitaxel were evaluated in this study. The patients were grouped per dose modification and use of granulocyte colony stimulating factor (G-CSF). The primary end point was OS; Hazard ratios (HR) for PFS and OS were calculated for patients who completed eight cycles of chemotherapy. Patients without dose modification were the referent group. All statistical analyses were performed using the R programming language and environment.

resultsA total of 738 patients were included in this study; 229 (31%) required dose modification, 509 did not. The two groups were well-balanced for demographic and prognostic factors. The adjusted hazard ratios (HR) for disease progression and death among dose-modified patients were: 1.43 (95% CI, 1.19-1.72, P < 0.001) and 1.26 (95% CI, 1.04-1.54, P = 0.021), respectively. Use of G-CSF was more frequent in dose-modified patients with an odds ratio (OR) of 3.63 (95% CI: 2.51-5.26, P < 0.001) compared to dose-unmodified patients.

conclusionDose-modified patients were at a higher risk of disease progression and death. The need for chemotherapy dose modification may identify patients at greater risk for adverse outcomes in advanced stage EOC and PPC.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCarcinoma, Ovarian EpithelialChemotherapy, AdjuvantCytoreduction Surgical ProceduresDisease-Free SurvivalDisease ProgressionDose-Response Relationship, DrugDoxorubicinFemaleGranulocyte Colony-Stimulating FactorHumansKaplan-Meier EstimateMiddle AgedNeoplasms, Glandular and EpithelialCarboplatinDoxorubicinGranulocyte Colony-Stimulating FactorPaclitaxelChemotherapyDose modificationDose reductionG-CSFOvarian cancerProgression

Identifiers

PMID30135020
PMCPMC6151871
OpenAlexW2887935494

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.