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


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
06 2020
Historique:
received: 27 11 2019
revised: 22 02 2020
accepted: 24 02 2020
pubmed: 8 3 2020
medline: 14 1 2021
entrez: 8 3 2020
Statut: ppublish

Résumé

This 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. This 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. Data 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). In 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.

Identifiants

pubmed: 32143914
pii: S0090-8258(20)30179-7
doi: 10.1016/j.ygyno.2020.02.033
pmc: PMC8022862
mid: NIHMS1674666
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

706-710

Subventions

Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors of this manuscript certify that they have no affiliations with or involvement in any organization or entity with any financial interest or non-financial interest in the subject matter or materials discussed in this manuscript.

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Auteurs

Kathryn A Mills (KA)

Division 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 Joshi (TV)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.

Lindsay West (L)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of North Carolina, Chapel Hill, NC, United States of America.

Michelle Kuznicki (M)

Department of Obstetrics and Gynecology, University of South Florida, Tampa, FL, United States of America.

Laura Kent (L)

Department of Obstetrics and Gynecology, University of South Florida, Tampa, FL, United States of America.

Alexis N Hokenstad (AN)

Division of Gynecologic Oncology, The Mayo Clinic, Rochester, MN, United States of America.

James C Cripe (JC)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, MO, United States of America.

Candice Woolfolk (C)

Division of Oncologic Biostatistics, Washington University, St. Louis, MO, United States of America.

Leigha Senter (L)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.

Jamie N Bakkum-Gamez (JN)

Division of Gynecologic Oncology, The Mayo Clinic, Rochester, MN, United States of America.

Robert M Wenham (RM)

Department of Gynecologic Oncology, Moffitt Cancer Center, Tampa, FL, United States of America.

David E Cohn (DE)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University, Columbus, OH, United States of America.

Victoria Bae-Jump (V)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of North Carolina, Chapel Hill, NC, United States of America.

Premal H Thaker (PH)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, MO, United States of America.

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