The impact of neoadjuvant relugolix on multi-dimensional patient-reported fatigue.

androgen deprivation therapy (ADT) facit fatigue prostate cancer quality of life relugolix 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: 05 04 2024
accepted: 24 07 2024
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: epublish

Résumé

Androgen deprivation therapy has been shown to improve cancer control when combined with radiotherapy. Relugolix is an oral GnRH receptor antagonist that achieves rapid profound testosterone suppression, which may increase the perception and/or impact of fatigue. This study sought to evaluate neoadjuvant relugolix-induced fatigue in prostate cancer patients prior to the start of stereotactic body radiation therapy (SBRT). Relugolix was initiated at least two months before SBRT. The 13-item Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire was collected at baseline and one hour prior to SBRT initiation. A five-point scale was used to score individual items. Overall scores range from 0-52 and individual item scores were converted to 0-100, with higher scores reflecting less fatigue. Five "experience" items explored self-perceptions of fatigue, and eight "impact" items sought to evaluate the effect of fatigue on daily activities. Items were evaluated for statistical significance (paired t-test, p < 0.05) and clinical significance (minimally important difference (MID); 0.5 standard deviation from baseline). Between March 2021 to December 2023, 89 men were treated at Georgetown with neoadjuvant relugolix and SBRT. Mean age was 71 years (range: 49-87). Median initiation of relugolix was 4.5 months prior to SBRT (range: 2-14.2 months). 93% patients achieved castration (testosterone levels ≤ 50 ng/dL) and 85% patients achieved profound castration (testosterone levels ≤ 20 ng/dL). 87 patients completed the FACIT-F questionnaire, with an average overall score of 45.6 at baseline and 41.0 at SBRT initiation. This difference was statistically and clinically significant (p < 0.01, MID = 3.55). Patients experienced an increase in fatigue for 12 of 13 items, with statistically significant changes for 11 items. Three of five experience items showed a clinically significant increase in fatigue. Only two of eight impact items were clinically significant. Our study shows that relugolix significantly increases fatigue, affecting multiple areas of life. While the fatigue does not appear to generally impact a patient's ability to carry out normal activities, patients demonstrate frustration with being too tired for these activities. It is essential for clinicians to counsel prostate cancer patients on the impact of neoadjuvant relugolix on quality-of-life issues like fatigue.

Identifiants

pubmed: 39188681
doi: 10.3389/fonc.2024.1412786
pmc: PMC11345208
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1412786

Informations de copyright

Copyright © 2024 Hsueh, Gallagher, Koh, Shah, Danner, Zwart, Ayoob, Kumar, Leger, Dawson, Suy 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.

Sarthak Shah (S)

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.

Sean P Collins (SP)

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

Classifications MeSH