Evidence map›Paper›PMID 32723679›Full record

Trial reportGynecologic oncology2020

Bevacizumab plus fosbretabulin in recurrent ovarian cancer: Overall survival and exploratory analyses of a randomized phase II NRG oncology/gynecologic oncology group study.

Krishnansu S Tewari, Michael W Sill, Robert L Coleman, Carol Aghajanian, Robert Mannel, Paul A DiSilvestro, Matthew Powell, Leslie M Randall, John Farley, Stephen C Rubin and 1 more

Open access · greenAbstract readClinical Trial, Phase IIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Gynecologic oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

11 authors at 10 institutions in 1 country.

Krishnansu S TewariUniversity of California, Irvine, Division of Gynecologic Oncology, Orange, CA, United States. Electronic address: ktewari@uci.edu.
Michael W SillNRG Oncology, Clinical Trial Development Division, Biostatistics & Bioinformatics, Roswell Park, Buffalo, NY 14263, United States. Electronic address: sillm@nrgoncology.org.
Robert L ColemanMD Anderson Cancer Center, Houston, TX, United States.
Carol AghajanianMemorial Sloan-Kettering Cancer Center, New York, NY, United States. Electronic address: aghajanc@MSKCC.org.
Robert MannelThe Peggy and Charles Stephenson Cancer Center, The University of Oklahoma Health Sciences Center, 800 NE 10(th) St., SOCC 6043, Oklahoma City, OK 73104, United States. Electronic address: robert-mannel@ouhsc.edu.
Paul A DiSilvestroWomen and Infants Hospital of Rhode Island, 101 Dudley St., Providence, RI 02905, United States. Electronic address: PDiSilvestro@WIHRI.org.
Matthew PowellWashington University School of Medicine, 4911 Barnes Jewish Hospital Plaza, St. Louis, MO 63110, United States. Electronic address: mpowell@wustl.edu.
Leslie M RandallUniversity of California, Irvine, Division of Gynecologic Oncology, Orange, CA, United States. Electronic address: Leslie.Randall@vcuhealth.org.
John FarleyCreighton University School of Medicine at St. Joseph's Hospital and Medical Center, Pheonix, AZ 85013, United States. Electronic address: John.farley@chw.edu.
Stephen C RubinFox Chase Cancer Center, 333 Cottman Ave., Philadelphia, PA 19111, United States. Electronic address: stephen.rubin@fccc.edu.
Bradley J MonkArizona Oncology (US Oncology Network), University of Arizona College of Medicine-Phoenix, Creighton University School of Medicine, St. Joseph's Hospital, Phoenix, AZ, United States. Electronic address: Bradley.Monk@usoncology.com.
University of California, Irvine · USBarnes-Jewish Hospital · USCreighton University · USFox Chase Cancer Center · USMemorial Sloan Kettering Cancer Center · USNRG Oncology · USSt. Joseph's Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Oklahoma Health Sciences Center · USWomen & Infants Hospital of Rhode Island · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 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, 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
A Lead Academic Participating Site in Oklahoma for the Design and Conduct of NCTN Clinical TrialsUG1CA233193 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Muhammad Furqan · 2019 to 2026
$13.7M
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 UG1 CA189867NCI NIH HHS UG1 CA233193NCI NIH HHS UG1 CA233290
6 · The paper itself

Abstract

objectiveTo explore the relationship between tumor size and response to combined anti-vascular targeted therapy using the anti-angiogenesis inhibitor, bevacizumab, and the tubulin-binding vascular disrupting agent, fosbretabulin.

methodsAn exploratory, post-hoc analysis of the randomized phase II trial, Gynecologic Oncology Group-0186I, was performed. One hundred and seven patients with recurrent ovarian carcinoma, treated with up to 3 prior regimens, were randomized to bevacizumab 15 mg/kg body weight with or without intravenous fosbretabulin 60 mg/m

resultsWith extended follow-up, the median PFS for bevacizumab plus fosbretabulin was 7.6  months as compared to 4.8  months with bevacizumab alone (HR 0.74; 90% CI, 0.54-1.02). Overall survival was similar in the experimental and control arms (25.2 vs 24.4 mos, respectively, HR 0.85; 90% CI, 0.59-1.22; p = .461). Eighty-one patients had measurable disease and median tumor size was 5.7  cm. In the ≤5.7  cm subgroup, the HR for progression or death was 0.77 (90% CI 0.45-1.31). Patients with tumors >5.7  cm (n = 40) had a HR for progression or death of 0.55; 90% CI, 0.32-0.96; p = .075).

conclusionsAlthough no significant survival benefit was observed, the trend showing a reduced HR for progression or death with increasing tumor size when fosbretabulin is added to bevacizumab compared to bevacizumab alone warrants further study.

Indexed as

AdultAntineoplastic Combined Chemotherapy ProtocolsBevacizumabFemaleFollow-Up StudiesHumansMiddle AgedNeoplasm Recurrence, LocalOvarian NeoplasmsOvaryProgression-Free SurvivalStilbenesTime FactorsTumor BurdenBevacizumabfosbretabulinStilbenesBevacizumabFosbretabulinOvarian cancerVascular disrupting agent

Identifiers

PMID32723679
PMCPMC7789907
OpenAlexW3043846144

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.