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激素敏感性寡转移复发前列腺癌的随机II期试验:立体定向消融放疗联合度伐利尤单抗(POSTCARD GETUG P13):研究方案

Randomized phase II trial in prostate cancer with hormone-sensitive OligometaSTatic relapse: Combining stereotactic ablative radiotherapy and durvalumab (POSTCARD GETUG P13): Study protocol.

作者信息

Rogé Maximilien, Pointreau Yoann, Sargos Paul, Meyer Emmanuel, Schick Ulrike, Hasbini Ali, Rio Emmanuel, Bera Guillaume, Ruffier Amandine, Quivrin Magali, Chasseray Mathieu, Latorzeff Igor, Martin Etienne, Guimas Valentine, Pommier Pascal, Leroy Thomas, Ronchin Philippe, Lepinoy Alexis, Grand Audrey, Cartier Lysian, Didas Ossama, Denis Fabrice, Libois Vincent, Blanc-Lapierre Audrey, Supiot Stéphane

机构信息

Department of Radiation Oncology, Centre Henri Becquerel, 1 rue d'Amiens, 76000 Rouen, France.

Department of Radiation Oncology, Centre Jean Bernard, 9 Rue Beauverger, 72100 Le Mans, France.

出版信息

Clin Transl Radiat Oncol. 2023 Mar 8;40:100613. doi: 10.1016/j.ctro.2023.100613. eCollection 2023 May.

Abstract

BACKGROUND

As in other solid tumors, increasing evidence indicates that patients diagnosed with a limited number of prostate cancer metastases, so-called oligometastases, have a better prognosis than patients with extensive metastatic disease. Stereotactic body radiotherapy (SBRT) is now considered an option in this population.Programmed death-1 (PD-1) and its ligands (PD-L1) are targeted by immune checkpoint inhibitors. Preclinical studies have shown that the tumor immune microenvironment changes when combining radiotherapy with immunotherapy, especially with hypofractionated radiotherapy.The oligometastatic setting appears to be the most relevant clinical situation for evaluating the immune response generated by radiotherapy and immune checkpoint inhibitors in patients with an intact immune system.We hypothesize that durvalumab will enhance the immune response following SBRT targeting oligometastatic lesions. Our purpose is to demonstrate, via a randomized 2:1 phase II trial, that SBRT (3 fractions) with durvalumab in oligometastatic hormone-sensitive prostate cancer patients would improve progression-free survival in patients with prostate cancer with up to 5 metastases compared to patients who exclusively received SBRT.

METHODS

This is a multicentric randomized phase II study in French academic hospitals. Patients with prostate cancer and up to 5 metastases (lymph node and/or bone) were randomized into a 2:1 ratio between Arm A (experimental group), corresponding to durvalumab and SBRT to the metastases, and Arm B (control group), corresponding to SBRT alone to the metastases. The study aims to accrue a total of 96 patients within 3 years. The primary endpoint is two-year progression-free survival and secondary endpoints include androgen deprivation therapy-free survival, quality of life, toxicity, prostate cancer specific survival, overall survival, and immune response.

DISCUSSION

The expected benefit for the patients in the experimental arm is longer life expectancy with acceptable toxicity. We also expect our study to provide data for better understanding the synergy between immunotherapy and radiotherapy in oligometastatic prostate cancer.

摘要

背景

与其他实体瘤一样,越来越多的证据表明,被诊断为前列腺癌转移灶数量有限(即所谓的寡转移)的患者,其预后优于广泛转移性疾病患者。立体定向体部放疗(SBRT)目前被认为是这一人群的一种选择。程序性死亡-1(PD-1)及其配体(PD-L1)是免疫检查点抑制剂的靶点。临床前研究表明,放疗与免疫疗法联合使用时,尤其是与低分割放疗联合使用时,肿瘤免疫微环境会发生变化。寡转移情况似乎是评估放疗和免疫检查点抑制剂在免疫系统完整的患者中产生的免疫反应的最相关临床情况。我们假设度伐利尤单抗将增强针对寡转移灶的SBRT后的免疫反应。我们的目的是通过一项随机2:1的II期试验证明,在寡转移激素敏感性前列腺癌患者中,SBRT(3次分割)联合度伐利尤单抗与单纯接受SBRT的患者相比,将改善转移灶最多为5个的前列腺癌患者的无进展生存期。

方法

这是一项在法国学术医院进行的多中心随机II期研究。前列腺癌且转移灶最多为5个(淋巴结和/或骨)的患者按2:1的比例随机分为A组(实验组),即度伐利尤单抗联合对转移灶进行SBRT,和B组(对照组),即仅对转移灶进行SBRT。该研究旨在在3年内共招募96名患者。主要终点是两年无进展生存期,次要终点包括无雄激素剥夺治疗生存期、生活质量、毒性、前列腺癌特异性生存期、总生存期和免疫反应。

讨论

实验组患者预期的获益是在可接受毒性的情况下延长预期寿命。我们还期望我们的研究能提供数据,以更好地理解寡转移前列腺癌中免疫疗法与放疗之间的协同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e66/10034400/d1186bdc448d/gr1.jpg

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