Impact of neoadjuvant relugolix on patient-reported sexual function and bother.

androgen deprivation therapy (ADT) bother prostate cancer relugolix sexual function stereotactic body radiation therapy (SBRT)

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2024
Historique:
received: 26 01 2024
accepted: 27 03 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: epublish

Résumé

Sexual function following local treatment for prostate cancer is an important quality of life concern. Relugolix is a novel oral GnRH receptor antagonist used in combination with radiation therapy in the treatment of unfavorable prostate cancer. It has been shown to achieve rapid and profound testosterone suppression. As a result, these very low testosterone levels may impact both sexual functioning and perceptions. This prospective study sought to assess neoadjuvant relugolix-induced sexual dysfunction prior to stereotactic body radiation therapy (SBRT). Between March 2021 and September 2023, 87 patients with localized prostate cancer were treated with neoadjuvant relugolix followed by SBRT per an institutional protocol. Sexual function and bother were assessed via the sexual domain of the validated Expanded Prostate Index Composite (EPIC-26) survey. Responses were collected for each patient at pre-treatment baseline and after several months of relugolix. A Utilization of Sexual Medications/Devices questionnaire was administered at the same time points to assess erectile aid usage. The median age was 72 years and 43% of patients were non-white. The median baseline Sexual Health Inventory for Men (SHIM) score was 13 and 41.7% of patients utilized sexual aids prior to relugolix. Patients initiated relugolix at a median of 4.5 months (2-14 months) prior to SBRT. 95% and 87% of patients achieved effective castration (≤ 50 ng/dL) and profound castration (< 20 ng/dl) at SBRT initiation, respectively. Ability to have an erection, ability to reach orgasm, quality of erections, frequency of erections, and overall sexual function significantly declined following relugolix. There was a non- significant increase in sexual bother. In concordance with known side effects of androgen deprivation therapy (ADT), neoadjuvant relugolix was associated with a significant decline in self-reported sexual function. However, patients indicated only a minimal and non-significant increase in bother. Future investigations should compare outcomes while on relugolix directly to GnRH agonist-induced sexual dysfunction.

Identifiants

pubmed: 38665954
doi: 10.3389/fonc.2024.1377103
pmc: PMC11043501
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1377103

Informations de copyright

Copyright © 2024 Hsueh, Gallagher, Koh, Eden, Shah, Wells, Danner, Zwart, Ayoob, Kumar, Leger, Dawson, Suy, Rubin and Collins.

Déclaration de conflit d'intérêts

SC serves as a clinical consultant to Sumitomo Pharma/Pfizer Inc. ND is on the Speaker Bureau for Sumitovant Biopharma. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Jessica Y Hsueh (JY)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Lindsey Gallagher (L)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Min Ji Koh (MJ)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Shaine Eden (S)

Systems Medicine Program, Department of Biochemistry and Molecular & Cellular Biology, Georgetown University Medical Center, Washington, DC, United States.

Sarthak Shah (S)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Markus Wells (M)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Malika Danner (M)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Alan Zwart (A)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Marilyn Ayoob (M)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Deepak Kumar (D)

Biotechnology Research Institute, North Carolina Central University, Durham, NC, United States.

Paul Leger (P)

Department of Oncology, Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington, DC, United States.

Nancy A Dawson (NA)

Department of Oncology, Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington, DC, United States.

Simeng Suy (S)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Rachel Rubin (R)

Department of Urology, MedStar Georgetown University Hospital, Washington, DC, United States.

Sean P Collins (SP)

Department of Radiation Medicine, MedStar Georgetown University Hospital, Washington, DC, United States.

Classifications MeSH