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
Department of Radiation Therapy, Centre Eugène Marquis, Rennes, France.
Department of Radiation Therapy, ARNAS Civico Palermo, Palermo, Italy.
Prostate Cancer Prostatic Dis. 2024 Jun 19. doi: 10.1038/s41391-024-00862-8.
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.
去势抵抗的出现与前列腺癌(PCa)患者的不良预后相关。转移性定向治疗已在多种疾病背景下进行研究,可能改善部分患者的预后。我们的系统评价旨在总结立体定向体部放疗(SBRT)治疗去势抵抗性前列腺癌(CRPC)的证据。
于2024年3月在PubMed上进行文献检索,使用关键词“SBRT”和“CRPC”,以及“立体定向消融放疗(SABR)”和“CRPC”。此次检索共获得108篇文章,纳入19篇。
文献主要为回顾性系列研究。在异时性寡进展的男性患者中,在一项随机II期试验中,SBRT联合雄激素受体通路抑制剂显著提高了无进展生存期(PFS),包括生化无进展生存期(风险比为0.35,p < 0.001)。在继续接受雄激素剥夺治疗(ADT)的患者中,生化无进展生存期(bPFS)在9.5个月至17.9个月之间,下次无全身治疗生存期(NEST - FS)可达2年。在诱导寡进展的男性患者中,SBRT使NEST - FS可达3年。SBRT耐受性良好,各研究报道3级毒性发生率均低于5%。
在寡转移CRPC患者群体中,SBRT可实现长期生化反应和无进展生存期。在寡进展情况下,SBRT可用于延长全身治疗的持续时间和疗效。然而,证据水平仍然很低,纳入前瞻性试验仍是这类患者的首选方案。