Evidence map›Paper›PMID 31759774›Full record

ArticleGynecologic oncology2020

Prospective follow-up of quality of life for participants undergoing risk-reducing salpingo-oophorectomy or ovarian cancer screening in GOG-0199: An NRG Oncology/GOG study.

Phuong L Mai, Helen Q Huang, Lari B Wenzel, Paul K Han, Richard P Moser, Gustavo C Rodriguez, John Boggess, Thomas J Rutherford, David E Cohn, Noah D Kauff and 8 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Gynecologic oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. 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

18 authors at 15 institutions in 2 countries.

Phuong L MaiClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, 20850-9772, USA. Electronic address: maip@upmc.edu.
Helen Q HuangNRG Oncology, Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, NY, 14263-0001, USA. Electronic address: hhuang@gogstats.org.
Lari B WenzelCenter for Health Policy Research, University of California, Irvine, Irvine CA, 92697, USA. Electronic address: lwenzel@uci.edu.
Paul K HanCenter for Outcomes Research and Evaluation, Maine Medical Center Research Institute, Portland, ME, 04101, USA. Electronic address: HANP@mmc.org.
Richard P MoserBehavioral Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, 20850-9761, USA. Electronic address: moserr@mail.nih.gov.
Gustavo C RodriguezDivision of Gynecologic Oncology, North Shore University Health System; Evanston, IL, 60201, USA. Electronic address: grodriguez@northshore.org.
John BoggessDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill; Raleigh NY 27607, USA. Electronic address: john_boggess@med.unc.edu.
Thomas J RutherfordYale University, Norwalk, CT, 06856, USA. Electronic address: thomas.rutherford@yale.edu.
David E CohnOhio State University, Columbus Cancer Council; GYN Oncology; Columbus, OH, 43026, USA. Electronic address: david.cohn@osumc.edu.
Noah D KauffGynecologic Medical Oncology Service, Memorial Sloan-Kettering Cancer Center; Surgery Department; New York, NY, 10065, USA. Electronic address: nkauff@northwell.edu.
Kelly-Anne PhillipsPeter MacCallum Cancer Centre, Division of Cancer Medicine, Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, 300 AU, Australia. Electronic address: kelly.phillips@petermac.org.
Kelly WilkinsonUniversity of Mississippi Medical Center, Dept. of Hematology/Oncology, Jackson, MS, 39216, USA. Electronic address: kjeanes@umc.edu.
Robert M WenhamH. Lee Moffitt Cancer Center & Research Institute, Gynecology Oncology Division; Tampa, FL, 33612-9497, USA. Electronic address: robert.wenham@moffitt.org.
Chad HamiltonWalter Reed Army Medical Center, Bethesda, MD, 20889, USA. Electronic address: chad.a.hamilton.mil@health.mil.
Matthew A PowellWashington University School of Medicine, Saint Louis, MO, 63110, USA. Electronic address: mpowell@wustl.edu.
Joan L WalkerStephenson Cancer Center, Department of Gynecologic Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA. Electronic address: joan-walker@ouhsc.edu.
Mark H GreeneClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, 20850-9772, USA. Electronic address: greenem@mail.nih.gov.
Martee L HensleyGynecologic Medical Oncology Service, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY, 10065, USA. Electronic address: hensleym@mskcc.org.
National Cancer Institute · USCornell University · USDivision of Cancer Epidemiology and GeneticsMaine Medical Center · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USNorthShore University HealthSystem · USNRG Oncology · USUniversity of California, Irvine · USUniversity of Melbourne · AUUniversity of Mississippi Medical Center · USUniversity of North Carolina at Chapel Hill · USUniversity of Oklahoma Health Sciences Center · USWashington University in St. Louis · USYale University · US

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 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
GYNECOLOGIC ONCOLOGY GROUP HEADQUARTERSU10CA027469 · NCI · GYNECOLOGIC ONCOLOGY GROUP · PI DISAIA, PHILIP J. · 1985 to 2013
$132.6M
Clinical Genetic Studies of Familial and Hereditary Cancer SyndromesZIACP010144 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SAVAGE, SHARON A. · 2009 to 2025
$111.8M
GYNECOLOGIC ONCOLOGY GROUP STATISTICAL OFFICEU10CA037517 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI BLESSING, JOHN A · 1985 to 2013
$67.4M
GYNECOLOGIC ONCOLOGY GROUPU10CA101165 · NCI · GYNECOLOGIC ONCOLOGY GROUP · PI DISAIA, PHILIP J. · 2003 to 2014
$43.1M
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
WASHINGTON UNIVERSITY / SITEMAN CANCER CENTER LEAD ACADEMIC SITEUG1CA233339 · NCI · WASHINGTON UNIVERSITY · PI NANCY L BARTLETT, Clifford Grant Robinson · 2019 to 2026
$11.3M
OSU as a Network Lead Academic Participating Site for the NCI NCTNUG1CA233331 · NCI · OHIO STATE UNIVERSITY · PI John L. Hays, Dwight H. Owen · 2019 to 2026
$8.9M
MaineHealth Cancer Care Network (MHCCN) and NCORP Activities across the LifespanUG1CA239771 · NCI · MAINEHEALTH · PI Leslie Bradford, Christine Lu-Emerson · 2019 to 2026
$7.9M
Intramural NIH HHS ZIA CP010144NCI NIH HHS HHSN261201300003CNCI NIH HHS P30 CA008748NCI NIH HHS U10 CA027469NCI NIH HHS U10 CA037517NCI NIH HHS U10 CA101165NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868NCI NIH HHS UG1 CA189867NCI NIH HHS UG1 CA233191NCI NIH HHS UG1 CA233193NCI NIH HHS UG1 CA233331NCI NIH HHS UG1 CA233339NCI NIH HHS UG1 CA239771
6 · The paper itself

Abstract

backgroundRisk-reducing salpingo-oophorectomy (RRSO) and ovarian cancer screening (OCS) are management options for women at increased risk of ovarian cancer. Long-term effects of these interventions on quality of life (QOL) are not well understood.

methodsGOG-0199 is a prospective cohort study of women at increased ovarian cancer risk who chose either RRSO or OCS as their risk management intervention. At study entry, 6, 12, 24 and 60 months of follow-up, participants completed the QOL questionnaire, which included the Medical Outcome Study Short Form-36, the Impact of Events Scales, the Center for Epidemiological Studies Depression Scale, the State-Trait Anxiety Inventory, the Functional Assessment of Cancer Therapy - Endocrine Subscale, and the Sexual Activity Questionnaire. QOL measures were compared between the RRSO and OCS cohort at baseline and over time.

resultsFive-hundred-sixty-two participants in the RRSO cohort and 1,010 in the OCS completed the baseline and at least one follow-up questionnaire. At baseline, participants selecting RRSO reported lower health-related QOL (HRQOL), greater ovarian cancer-related stress, greater anxiety, and more depressive symptomatology, which improved during follow-up, especially for ovarian cancer-related stress. Screening was not found to adversely impact HRQOL. Hormone-related menopausal symptoms worsened and sexual functioning declined during follow-up in both cohorts, but more so among participants who underwent RRSO.

conclusionsHRQOL improved after surgery among women who chose RRSO and remained stable among participants undergoing screening. The adverse effects of RRSO and screening on short-term and long-term sexual activity and sexual functioning warrant consideration in the decision-making process for high-risk women.

Indexed as

AdultAgedCohort StudiesEarly Detection of CancerFemaleFollow-Up StudiesHumansMiddle AgedOvarian NeoplasmsProspective StudiesQuality of LifeSalpingo-oophorectomy

Identifiers

PMID31759774
PMCPMC6980744
OpenAlexW2991069503

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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.