Nonrandomized Comparison of Efficacy and Side Effects of Bicalutamide Compared With Luteinizing Hormone-Releasing Hormone (LHRH) Analogs in Combination With Radiation Therapy in the CHHiP Trial.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 06 2022
Historique:
received: 20 05 2021
revised: 19 12 2021
accepted: 23 12 2021
pubmed: 13 1 2022
medline: 18 5 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

CHHiP is a randomized trial evaluating moderately hypofractionated radiation therapy for treatment of localized prostate cancer. Of all participants, 97% of them had concurrent short-course hormone therapy (HT), either luteinizing hormone-releasing hormone analog (LHRHa) or 150 mg of bicalutamide daily. This exploratory analysis compares efficacy and side effects in a nonrandomized comparison. In our study, 2700 patients received LHRHa and 403 received bicalutamide. The primary endpoint was biochemical/clinical failure. Groups were compared with Cox regression adjusted for various prognostic factors and stratified by radiation therapy dose. A key secondary endpoint was erectile dysfunction (ED) assessed by clinicians (using scores from Late Effects on Normal Tissues: Subjective/Objective/Management [LENT-SOM] subjective erectile function for vaginal penetration) and patients (single items within the University of California-Los Angeles Prostate Cancer Index [UCLA PCI] and Expanded Prostate Cancer Index Composite [EPIC]-50 questionnaires) at 2 years and compared between HT regimens by χ Bicalutamide patients were significantly younger (median 67 vs 69 years LHRHa). Median follow-up was 9.3 years. There was no difference in biochemical or clinical failure with an adjusted hazard ratio or 0.97 (95% confidence interval, 0.77-1.23; P = .8). At 2 years, grade ≥2 LENT-SOM ED was reported in significantly more LHRHa patients (313 out of 590; 53%) versus bicalutamide (17 out of 68; 25%) (P < .0001). There were no differences in ED seen with UCLA-PCI and EPIC-50 questionnaires. In this nonrandomized comparison, there was no evidence of a difference in efficacy according to type of HT received. Bicalutamide preserved clinician assessed (LENT-SOM) erectile function at 2 years but patient-reported outcomes were similar between groups.

Identifiants

pubmed: 35017008
pii: S0360-3016(21)03433-7
doi: 10.1016/j.ijrobp.2021.12.160
pmc: PMC9119688
pii:
doi:

Substances chimiques

Androgen Antagonists 0
Anilides 0
Nitriles 0
Tosyl Compounds 0
Gonadotropin-Releasing Hormone 33515-09-2
bicalutamide A0Z3NAU9DP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

305-315

Subventions

Organisme : Cancer Research UK
ID : C46/A10588
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C33589/A28284
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C46/A3976
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 7253
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 12518
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C33589/A19727
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Alison Tree (A)

Royal Marsden NHS Foundation Trust, London, United Kingdom; Institute of Cancer Research, London, United Kingdom. Electronic address: Alison.tree@icr.ac.uk.

Clare Griffin (C)

Institute of Cancer Research, London, United Kingdom.

Isabel Syndikus (I)

Clatterbridge Cancer Centre, Wirral, United Kingdom.

Alison Birtle (A)

Royal Preston Hospital, Preston, United Kingdom.

Ananya Choudhury (A)

University of Manchester, Manchester, United Kingdom.

John Graham (J)

Beatson Oncology Centre, Glasgow, United Kingdom.

Catherine Ferguson (C)

Weston Park Hospital, Sheffield, United Kingdom.

Vincent Khoo (V)

Royal Marsden NHS Foundation Trust, London, United Kingdom; Institute of Cancer Research, London, United Kingdom.

Zafar Malik (Z)

Whiston Hospital, Merseyside, United Kingdom.

Joe O'Sullivan (J)

Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Miguel Panades (M)

Lincoln County Hospital, Lincoln, United Kingdom.

Chris Parker (C)

Royal Marsden NHS Foundation Trust, London, United Kingdom; Institute of Cancer Research, London, United Kingdom.

Yvonne Rimmer (Y)

Addenbrooke's Hospital, Cambridge, United Kingdom.

Christopher Scrase (C)

Ipswich Hospital, Ipswich, United Kingdom.

John Staffurth (J)

Cardiff University/Velindre Cancer Centre, Cardiff, United Kingdom.

David Dearnaley (D)

Royal Marsden NHS Foundation Trust, London, United Kingdom; Institute of Cancer Research, London, United Kingdom.

Emma Hall (E)

Institute of Cancer Research, London, United Kingdom.

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Classifications MeSH