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The current landscape of stereotactic body radiation therapy for metastatic castration-resistant prostate cancer.
Le Guevelou, Jennifer; Cuccia, Francesco; Flippot, Ronan; Ferrera, Giuseppe; Terlizzi, Mario; Zilli, Thomas; De Crevoisier, Renaud; Hannoun-Levi, Jean-Michel; Supiot, Stephane; Sargos, Paul; Pasquier, David.
Afiliação
  • Le Guevelou J; Department of Radiation Therapy, Centre Eugène Marquis, Rennes, France. Jennifer.leguevelou@gmail.com.
  • Cuccia F; Department of Radiation Therapy, ARNAS Civico Palermo, Palermo, Italy.
  • Flippot R; Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.
  • Ferrera G; Department of Radiation Therapy, ARNAS Civico Palermo, Palermo, Italy.
  • Terlizzi M; Department of Radiation Therapy, Institut Gustave Roussy, Villejuif, France.
  • Zilli T; Department of Radiation Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
  • De Crevoisier R; Università della Svizzera Italiana, Lugano, Switzerland.
  • Hannoun-Levi JM; Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Supiot S; Department of Radiation Therapy, Centre Eugène Marquis, Rennes, France.
  • Sargos P; Department of Radiation Oncology, Centre Antoine Lacassagne, University Côte d'Azur, Nice, France.
  • Pasquier D; Department of Radiation Oncology, Institut de Cancérologie de l'Ouest, Nantes, France.
Article em En | MEDLINE | ID: mdl-38898265
ABSTRACT

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:

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:

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:

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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França