The current landscape of stereotactic body radiation therapy for metastatic castration-resistant prostate cancer.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
19 Jun 2024
Historique:
received: 17 05 2024
accepted: 13 06 2024
revised: 08 06 2024
medline: 20 6 2024
pubmed: 20 6 2024
entrez: 19 6 2024
Statut: aheadofprint

Résumé

The onset of castration-resistance is associated with dismal outcomes in patients with prostate cancer (PCa). Metastasis directed therapy has been investigated in multiple disease settings and may improve outcomes in selected patients. Our systematic review aims to summarize evidence with stereotactic body radiotherapy (SBRT) in castration-resistant prostate cancer (CRPC). The literature search was performed on March 2024, on Pubmed, using the keywords "SBRT" AND "CRPC", and "stereotactic ablative radiotherapy (SABR)" AND "CRPC". This search retrieved a total of 108 articles, 19 were included. The literature is largely dominated by retrospective series. In men with metachronous oligoprogression, SBRT with androgen receptor pathway inhibitor significantly increased progression-free survival (PFS) including biochemical progression-free survival in a randomized phase II trial (hazard ratio of 0.35, p < 0.001). In patients continuing ADT, the bPFS ranged between 9.5 months to 17.9 months, and next systemic treatment-free survival (NEST-FS) reached up to 2 years. In men with induced oligoprogression, SBRT enabled NEST-FS up to 3 years. SBRT was well tolerated, with less than 5% grade 3 toxicity reported across studies. In the population of patients with oligometastatic CRPC, SBRT enables long-term biochemical response and PFS. In the oligoprogressive setting, SBRT could be integrated to prolong the duration and efficacy of systemic therapies. Nevertheless, the level of evidence remains very low and inclusion within prospective trials remain the preferred option for this population of patients.

Sections du résumé

BACKGROUND BACKGROUND
The onset of castration-resistance is associated with dismal outcomes in patients with prostate cancer (PCa). Metastasis directed therapy has been investigated in multiple disease settings and may improve outcomes in selected patients. Our systematic review aims to summarize evidence with stereotactic body radiotherapy (SBRT) in castration-resistant prostate cancer (CRPC).
METHODS METHODS
The literature search was performed on March 2024, on Pubmed, using the keywords "SBRT" AND "CRPC", and "stereotactic ablative radiotherapy (SABR)" AND "CRPC". This search retrieved a total of 108 articles, 19 were included.
RESULTS RESULTS
The literature is largely dominated by retrospective series. In men with metachronous oligoprogression, SBRT with androgen receptor pathway inhibitor significantly increased progression-free survival (PFS) including biochemical progression-free survival in a randomized phase II trial (hazard ratio of 0.35, p < 0.001). In patients continuing ADT, the bPFS ranged between 9.5 months to 17.9 months, and next systemic treatment-free survival (NEST-FS) reached up to 2 years. In men with induced oligoprogression, SBRT enabled NEST-FS up to 3 years. SBRT was well tolerated, with less than 5% grade 3 toxicity reported across studies.
CONCLUSION CONCLUSIONS
In the population of patients with oligometastatic CRPC, SBRT enables long-term biochemical response and PFS. In the oligoprogressive setting, SBRT could be integrated to prolong the duration and efficacy of systemic therapies. Nevertheless, the level of evidence remains very low and inclusion within prospective trials remain the preferred option for this population of patients.

Identifiants

pubmed: 38898265
doi: 10.1038/s41391-024-00862-8
pii: 10.1038/s41391-024-00862-8
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Jennifer Le Guevelou (J)

Department of Radiation Therapy, Centre Eugène Marquis, Rennes, France. Jennifer.leguevelou@gmail.com.

Francesco Cuccia (F)

Department of Radiation Therapy, ARNAS Civico Palermo, Palermo, Italy.

Ronan Flippot (R)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

Giuseppe Ferrera (G)

Department of Radiation Therapy, ARNAS Civico Palermo, Palermo, Italy.

Mario Terlizzi (M)

Department of Radiation Therapy, Institut Gustave Roussy, Villejuif, France.

Thomas Zilli (T)

Department of Radiation Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Università della Svizzera Italiana, Lugano, Switzerland.
Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Renaud De Crevoisier (R)

Department of Radiation Therapy, Centre Eugène Marquis, Rennes, France.

Jean-Michel Hannoun-Levi (JM)

Department of Radiation Oncology, Centre Antoine Lacassagne, University Côte d'Azur, Nice, France.

Stephane Supiot (S)

Department of Radiation Oncology, Institut de Cancérologie de l'Ouest, Nantes, France.

Paul Sargos (P)

Department of Radiation Oncology, Institut Bergonié, Bordeaux, France.

David Pasquier (D)

Academic Department of Radiation Oncology, Centre Oscar Lambret, Lille, France.
Lille University, CRIStAL UMR CNRS 9189, Lille, France.

Classifications MeSH