Evidence map›Paper›PMID 26616224›Full record

Trial reportGynecologic oncology2016

A phase II study of paclitaxel for the treatment of ovarian stromal tumors: An NRG Oncology/ Gynecologic Oncology Group Study.

Elizabeth R Burton, Mark Brady, Howard D Homesley, Peter G Rose, Toshiaki Nakamura, Joshua P Kesterson, Jacob Rotmensch, J Tate Thigpen, Linda Van Le

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Gynecologic oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Open-label phase II clinical trial of orteronel (TAK-700) in metastatic or advanced non-resectable granulosa cell ovarian tumors: the Greko II study (GETHI2013-01).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Trial
  3. Open-label phase II clinical trial of ketoconazole as CYP17 inhibitor in metastatic or advanced non-resectable granulosa cell ovarian tumors: the GREKO (GRanulosa Et KetOconazole) trial, GETHI 2011-03.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Trial
  4. Article
  5. Review
  6. Article
  7. Review
  8. Non-Epithelial Ovarian Cancers: How Much Do We Really Know?International journal of environmental research and public health · 2022
    Review
  9. Article
  10. Review
  11. 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

9 authors at 9 institutions in 2 countries.

Elizabeth R BurtonHanjani Institute for Gynecologic Oncology, Abington Memorial Hospital, 1200 Old York Road, Abington, PA 19001, United States. Electronic address: eburton@abingtonhealth.org.
Mark BradyNRG Oncology Statistical Office, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, United States. Electronic address: mbrady@gogstats.org.
Howard D HomesleyEast Carolina University, Greensville, NC 27858, United States. Electronic address: homesleyh@ecu.edu.
Peter G RoseCleveland Clinic Foundation, Cleveland, OH 44195, United States. Electronic address: rosep@ccf.org.
Toshiaki NakamuraKagoshima City Hospital, Department of OB/GYN, Kagoshima City 892 8580, Japan. Electronic address: nakamura@ml.kch.kagoshima.kagoshima.jp.
Joshua P KestersonHershey Medical Center, GYN/Oncology, Hershey, PA 17033, United States. Electronic address: jkesterson@hmc.psu.edu.
Jacob RotmenschRush-Presbyterian St. Lukes Medical Center, Chicago, IL 60612, United States. Electronic address: Jacob_rotmensch@rush.edu.
J Tate ThigpenUniversity of Mississippi Medical Center, Jackson, MS 39216, United States. Electronic address: jthigpen@umc.edu.
Linda Van LeUniversity of North Carolina School of Medicine, 101 Manning Drive, Chapel Hill, NC 27514, United States. Electronic address: lvl@med.unc.edu.
Abington Memorial Hospital · USCleveland Clinic · USEast Carolina University · USHershey (United States) · USJackson Memorial Hospital · USKagoshima City Hospital · JPRoswell Park Comprehensive Cancer Center · USRush University Medical Center · USUniversity of North Carolina at Chapel Hill · 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 Mei-Yin C Polley · 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 1U10 CA180822NCI NIH HHS 1U10 CA180868NCI NIH HHS CA 27469NCI NIH HHS CA 37517NCI NIH HHS U10 CA027469NCI NIH HHS U10 CA037517NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868
6 · The paper itself

Abstract

objectiveTo estimate the probability of complete clinical response and toxicity of paclitaxel as second-line chemotherapy in measurable disease patients with malignant tumors of the ovarian stroma, and to evaluate the value of inhibin for predicting response.

methodsThirty-one patients with histologically confirmed ovarian stromal tumor were enrolled from 2000 to 2013. Patients were required to have measurable recurrent disease, and to have received only one prior chemotherapy regimen. Paclitaxel 175 mg/m2 was administered over a 3 hour infusion, cycling every 21 days. Inhibin levels were drawn within two weeks of initiation of treatment.

resultsOf 31 women enrolled, there was only one complete response (3.2%), and partial response in eight of 31 cases (25.8%). The pretreatment inhibin level for the single patient who had complete response was 88 pg/mL. Median progression-free survival was 10.0 months and overall survival was 73.6 months. Myelosuppression was common with 12 of 31 patients (38.7%) suffering grade 3 or 4 neutropenia, leukopenia, or anemia.

conclusionThere were too few complete responses to warrant continued evaluation of paclitaxel as a single agent treatment for women with recurrent malignant ovarian stromal tumors with measurable disease according to the primary objective of the study. Toxicity of the regimen was acceptable. Pretreatment inhibin is not a reliable tumor marker as it was not elevated in the majority of patients.

Indexed as

AdultAntineoplastic Agents, PhytogenicDisease-Free SurvivalFemaleHumansMiddle AgedOvarian NeoplasmsPaclitaxelSex Cord-Gonadal Stromal TumorsAntineoplastic Agents, PhytogenicPaclitaxelPaclitaxelStromal tumor of ovary

Identifiers

PMID26616224
PMCPMC5065725
OpenAlexW2175293021

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.