Evidence map›Paper›PMID 32143914›Full record

ArticleGynecologic oncology2020

Is hormonal therapy after risk-reducing salpingo-oophorectomy associated with an increased risk of malignancy in pathogenic variant carriers?

Kathryn A Mills, Tanvi V Joshi, Lindsay West, Michelle Kuznicki, Laura Kent, Alexis N Hokenstad, James C Cripe, Candice Woolfolk, Leigha Senter, Jamie N Bakkum-Gamez and 4 more

Open access · greenAbstract read
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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 6 institutions in 1 country.

Kathryn A MillsDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, MO, United States of America. Electronic address: kmills6@bsd.uchicago.edu.
Tanvi V JoshiDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.
Lindsay WestDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of North Carolina, Chapel Hill, NC, United States of America.
Michelle KuznickiDepartment of Obstetrics and Gynecology, University of South Florida, Tampa, FL, United States of America.
Laura KentDepartment of Obstetrics and Gynecology, University of South Florida, Tampa, FL, United States of America.
Alexis N HokenstadDivision of Gynecologic Oncology, The Mayo Clinic, Rochester, MN, United States of America.
James C CripeDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, MO, United States of America.
Candice WoolfolkDivision of Oncologic Biostatistics, Washington University, St. Louis, MO, United States of America.
Leigha SenterDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.
Jamie N Bakkum-GamezDivision of Gynecologic Oncology, The Mayo Clinic, Rochester, MN, United States of America.
Robert M WenhamDepartment of Gynecologic Oncology, Moffitt Cancer Center, Tampa, FL, United States of America.
David E CohnDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.
Victoria Bae-JumpDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of North Carolina, Chapel Hill, NC, United States of America.
Premal H ThakerDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, MO, United States of America.
Washington University in St. Louis · USThe Ohio State University · USMayo Clinic · USUniversity of North Carolina at Chapel Hill · USUniversity of South Florida · USMoffitt Cancer Center · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

objectivesThis study aimed to assess the association between hormone replacement therapy and the incidence of subsequent malignancies in patients who underwent risk-reducing salpingo-oophorectomy and had mutations predisposing them to Müllerian cancers.

methodsThis Institutional Review Board-approved retrospective study was performed at five academic institutions. Women were included if they were age 18-51 years, had one or more confirmed germline highly penetrant pathogenic variants, and underwent risk-reducing salpingo-oophorectomy. Patients with a prior malignancy were excluded. Clinicodemographic data were collected by chart review. Patients with no documented contact for one year prior to study termination were called to confirm duration of hormone use and occurrence of secondary outcomes. Hormone replacement therapy included any combination of estrogen or progesterone.

resultsData were analyzed for 159 women, of which 82 received hormone replacement therapy and 77 did not. In both groups an average of 6 years since risk reduction had passed. The patients treated with hormone replacement therapy did not have a higher risk of subsequent malignancy than those not treated with hormone replacement therapy (6 out of 82 vs. 7 out of 77, P = .68). Patients who received hormone replacement therapy were younger than those who did not receive hormone replacement therapy (39.0 vs. 43.9 years, P < .01) and were more likely to have undergone other risk reductive procedures including mastectomy and/or hysterectomy, though this difference was not statistically significant (69.5% vs. 55.8%, P = .07).

conclusionsIn this multi-institution retrospective study of data from patients with high-risk variant carriers who underwent risk-reducing salpingo-oophorectomy, there was no statistically significant difference in the incidence of malignancy between women who did and did not receive hormone replacement therapy.

Indexed as

AdolescentAdultFemaleGenetic Predisposition to DiseaseGenital Neoplasms, FemaleHormone Replacement TherapyHumansMiddle AgedRisk Reduction BehaviorSalpingo-oophorectomyYoung AdultHormone replacement therapyPathogenic variant carriersRisk reduction surgery

Identifiers

PMID32143914
PMCPMC8022862
OpenAlexW3010042214

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Registered trials

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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.