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
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

100613

Informations 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

Auteurs

Maximilien Rogé (M)

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

Yoann Pointreau (Y)

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

Paul Sargos (P)

Department of Radiation Oncology, Institut Bergonié, 229 Cr de l'Argonne, 33076 Bordeaux, France.

Emmanuel Meyer (E)

Department of Radiation Oncology, Centre François Baclesse, 3 Av. du General Harris, 14000 Caen, France.

Ulrike Schick (U)

Department of Radiation Oncology, University Hospital Morvan, 2 avenue Foch, 29200 Brest, France.

Ali Hasbini (A)

Department of Radiation Oncology, Clinique Pasteur, 32 Rue Auguste Kervern, 29200 Brest, France.

Emmanuel Rio (E)

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

Guillaume Bera (G)

Department of Radiation Oncology, Centre Hospitalier de Bretagne Sud, 5 avenue de Choiseul, 56322 Lorient, France.

Amandine Ruffier (A)

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

Magali Quivrin (M)

Department of Radiation Oncology, Georges-François Leclerc Cancer Centre-UNICANCER, 1 Rue Professeur Marion, 21000 Dijon, France.

Mathieu Chasseray (M)

Department of Radiation Oncology, University Hospital Morvan, 2 avenue Foch, 29200 Brest, France.

Igor Latorzeff (I)

Department of Radiation Oncology, Oncorad Clinique Pasteur, 1, rue de la Petite Vitesse, 31 000 Toulouse, France.

Etienne Martin (E)

Department of Radiation Oncology, Georges-François Leclerc Cancer Centre-UNICANCER, 1 Rue Professeur Marion, 21000 Dijon, France.

Valentine Guimas (V)

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

Pascal Pommier (P)

Department of Radiation Oncology, Centre Léon Bérard, 28 Prom. Léa et Napoléon Bullukian, 69008 Lyon, France.

Thomas Leroy (T)

Department of Radiation Oncology, Clinique des Dentellières, 8 av Vauban, 59300 Valenciennes, France.

Philippe Ronchin (P)

Department of Radiation Oncology, Centre Azureen de Cancerologie, 1 Place Docteur Jean Luc Broquerie, 06250 Mougins, France.

Alexis Lepinoy (A)

Department of Radiation Oncology, Bourgogne Institute of Oncology, 18 Cr General de Gaulle, 21000 Dijon, France.

Audrey Grand (A)

Department of Radiation Oncology Center Hospitalier Lyon Sud, 165 Chem. du Grand Revoyet, 69495 Pierre-Bénite, France.

Lysian Cartier (L)

Department of Radiation Oncology, Institut Sainte Catherine, 250 Chem. de Baigne Pieds, 84918 Avignon, France.

Ossama Didas (O)

Department of Radiation Oncology, Hôpital Bretonneau, CHU de Tours, 2, boulevard Tonnellé, 37044 Tours, France.

Fabrice Denis (F)

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

Vincent Libois (V)

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

Audrey Blanc-Lapierre (A)

Department of Biostatistics, Institut de Cancérologie de l'Ouest, Bd Professeur Jacques Monod, 44800 Saint Herblain, France.

Stéphane Supiot (S)

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

Classifications MeSH