Randomized phase II trial in prostate cancer with hormone-sensitive OligometaSTatic relapse: Combining stereotactic ablative radiotherapy and durvalumab (POSTCARD GETUG P13): Study protocol.
Immunotherapy
Oligometastases
Oligorecurrent
Prostate cancer
Stereotactic body radiotherapy
Journal
Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416
Informations de publication
Date de publication:
May 2023
May 2023
Historique:
received:
21
02
2023
revised:
04
03
2023
accepted:
05
03
2023
entrez:
27
3
2023
pubmed:
28
3
2023
medline:
28
3
2023
Statut:
epublish
Résumé
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. 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. 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.
Sections du résumé
Background
UNASSIGNED
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
UNASSIGNED
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
UNASSIGNED
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.
Identifiants
pubmed: 36968576
doi: 10.1016/j.ctro.2023.100613
pii: S2405-6308(23)00038-1
pmc: PMC10034400
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100613Informations de copyright
© 2023 The Authors.
Déclaration de conflit d'intérêts
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Références
J Clin Oncol. 2018 Feb 10;36(5):446-453
pubmed: 29240541
Front Oncol. 2021 Sep 14;11:744679
pubmed: 34595122
Cell Immunol. 2014 Jul;290(1):72-9
pubmed: 24908630
J Clin Oncol. 2020 Feb 10;38(5):395-405
pubmed: 31774688
Int J Radiat Oncol Biol Phys. 2012 Aug 1;83(5):e597-605
pubmed: 22608954
Stat Med. 2001 Mar 30;20(6):859-66
pubmed: 11252008
Cancer Cell. 2020 Oct 12;38(4):489-499.e3
pubmed: 32916128
JAMA Oncol. 2020 May 1;6(5):650-659
pubmed: 32215577
Br J Cancer. 2020 Sep;123(7):1089-1100
pubmed: 32641865
Lancet Oncol. 2017 Mar;18(3):e143-e152
pubmed: 28271869
Eur Urol. 2018 Oct;74(4):455-462
pubmed: 30227924
Lancet Oncol. 2019 Oct;20(10):1370-1385
pubmed: 31427204
Radiat Oncol. 2014 Dec 11;9:258
pubmed: 25497220
Ann Oncol. 2013 Nov;24(11):2881-6
pubmed: 23946329
Front Immunol. 2018 Jul 31;9:1786
pubmed: 30108594
Front Oncol. 2013 Dec 03;3:293
pubmed: 24350058
Clin Oncol (R Coll Radiol). 2018 Jan;30(1):5-14
pubmed: 29033164
Int J Cancer. 2020 Jan 1;146(1):161-168
pubmed: 31199504
Prostate. 2014 Feb;74(3):297-305
pubmed: 24395565
N Engl J Med. 2017 Mar 16;376(11):1015-1026
pubmed: 28212060