An Expert Review on the Combination of Relugolix With Definitive Radiation Therapy for Prostate Cancer.


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: 16 10 2021
revised: 05 12 2021
accepted: 06 12 2021
pubmed: 20 12 2021
medline: 18 5 2022
entrez: 19 12 2021
Statut: ppublish

Résumé

Androgen deprivation therapy (ADT) is an integral component in the management of prostate cancer across multiple disease states. Traditionally, luteinizing hormone-releasing hormone (LHRH) agonists constituted the backbone of ADT. However, gonadotropin-releasing hormone receptor hormone (GnRH) antagonists also are available, which offer faster testosterone suppression and reduced likelihood of ADT-related adverse effects compared with LHRH agonists, including the potential for fewer ADT-associated major cardiac events. Until recently, all forms of LHRH agonists and GnRH antagonist formulations were of parenteral administration. However, recently relugolix gained Food and Drug Administration approval as the first oral GnRH antagonist. Relugolix achieves faster and more complete testosterone suppression compared with an LHRH agonist. This translates to more rapid prostate-specific antigen response compared with LHRH agonists. After discontinuation of relugolix, testosterone recovers faster than after GnRH agonists or injectable GnRH antagonist therapy. Overall, these factors provide opportunities for more precisely defined ADT duration when combined with radiation therapy. The rapid onset and offset of testosterone suppression with relugolix may require physicians to rethink the mechanism and goals of ADT when prescribing. As an oral formulation, relugolix enables patients to avoid pain and injection site reactions, limit extra office visits for injections, and achieve a shorter duration of experiencing the side effects of castrate testosterone levels. This convenience and tolerability may enhance physicians' willingness to prescribe ADT and patients' feeling of control during their ADT course, but the potential advantages are accompanied by the risks of patients choosing to discontinue therapy to escape side effects of ADT. This article focuses on different aspects of what is known and unknown regarding the optimal use of ADT and radiation therapy, and how relugolix, due to its properties, fit into our current treatment paradigms for localized prostate cancer.

Identifiants

pubmed: 34923058
pii: S0360-3016(21)03240-5
doi: 10.1016/j.ijrobp.2021.12.005
pii:
doi:

Substances chimiques

Androgen Antagonists 0
Phenylurea Compounds 0
Pyrimidinones 0
relugolix 0
Gonadotropin-Releasing Hormone 33515-09-2
Testosterone 3XMK78S47O

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

278-289

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Soumyajit Roy (S)

Department of Radiation Oncology, Rush University Medical Center, Chicago, Illinois.

Nicholas G Zaorsky (NG)

Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Hilary P Bagshaw (HP)

Department of Radiation Oncology, Stanford University, Palo Alto, California.

Alejandro Berlin (A)

Radiation Medicine Program, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.

Alison Tree (A)

Westmead Medical School, The University of Sydney, Sydney, Australia.

Sandra Turner (S)

Westmead Medical School, The University of Sydney, Sydney, Australia.

Bridget Koontz (B)

Department of Radiation Oncology, Duke University, Durham, North Carolina.

Paul Nguyen (P)

Department of Radiation Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.

Ronald Chen (R)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

Robert T Dess (RT)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

William C Jackson (WC)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

Amar U Kishan (AU)

Department of Radiation Oncology, University of California Los Angeles, Los Angeles, California.

Bradley Stish (B)

Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.

Himanshu Nagar (H)

Department of Radiation Oncology, Weill Cornell Medicine, New York, New York.

Edwin Posadas (E)

Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, Calfornia.

Phuoc T Tran (PT)

Department of Radiation Oncology, Johns Hopkins University, Baltimore, Maryland.

Abhishek Solanki (A)

Department of Radiation Oncology, Loyola University Medical Center, Chicago, Illinois.

Neal D Shore (ND)

Carolina Urologic Research Center, Myrtle Beach, South Carolina.

Gordon Guo (G)

Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Lee Ponsky (L)

Department of Urology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Jonathan E Shoag (JE)

Department of Urology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Alicia K Morgans (AK)

Department of Medicine, Northwestern University, Chicago, Illinois.

Jorge A Garcia (JA)

Department of Medicine, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Timothy N Showalter (TN)

Department of Radiation Oncology, University of Virginia; Charlottesville, Virginia.

Felix Y Feng (FY)

Department of Radiation Oncology, University of California San Francisco, San Francisco, California.

Daniel E Spratt (DE)

Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Cleveland, Ohio. Electronic address: daniel.spratt@uhhospitals.org.

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Classifications MeSH