Combination of Abiraterone Acetate, Prostate Bed Radiotherapy, and Luteinizing Hormone-releasing Hormone Agonists in Biochemically Relapsing Patients After Prostatectomy (CARLHA): A Phase 2 Clinical Trial.

Abiraterone acetate Biochemical recurrence Biomarkers Circulating tumor cells Hormone therapy Prostate bed radiotherapy Prostate cancer Salvage radiotherapy

Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
10 May 2024
Historique:
received: 12 02 2024
revised: 26 03 2024
accepted: 23 04 2024
medline: 12 5 2024
pubmed: 12 5 2024
entrez: 11 5 2024
Statut: aheadofprint

Résumé

The relevance of next-generation hormone therapies and circulating tumor cells (CTCs) are not elucidated in biochemical recurrence after prostatectomy. To evaluate the combination of abiraterone acetate plus prednisone (AAP), prostate bed radiotherapy (PBRT), and goserelin in biochemically relapsing men after prostatectomy, and to investigate the utility of CTCs. In this single-arm multicenter phase 2 trial, 46 biochemically relapsing men were enrolled between December 2012 and January 2019. The median follow-up was 47 mo. All patients received AAP 1000 mg daily (but 750 mg during PBRT), salvage PBRT, and goserelin. The primary outcome was 3-yr biochemical recurrence-free survival (bRFS) when prostate-specific antigen (PSA) levels were ≥0.2 ng/ml. The secondary outcomes included alternative bRFS (alt-bRFS) when PSA levels were ≥0.5 ng/ml and safety assessment. CTC count was assessed. The 3-yr bRFS and alt-bRFS were 81.5% (95% confidence interval or CI [66.4-90.3%]) and 95.6% (95% CI [83.5-98.9%]), respectively. The most common acute radiotherapy-related adverse effect (AE; all grades was pollakiuria (41.3%). The most common late AE (all grades) was urinary incontinence (15.2%). Grade 3-4 acute or late radiotherapy-related AEs were scarce. Most frequent AEs nonrelated to radiotherapy were hot flashes (76%), hypertension (63%), and hepatic cytolysis (50%, of which 20% were of grades 3-4). Of the patients, 11% had a CTC count of ≥5, which was correlated with poorer bRFS (p = 0.042) and alt-bRFS (p = 0.008). The association between CTC count and higher rates of relapse was independent of the baseline PSA level and PSA doubling time (p = 0.42 and p = 0.09, respectively). This study was nonrandomized with a limited number of patients, and few clinical events were reported. Adding AAP to salvage radiation therapy and goserelin resulted in high bRFS and alt-bRFS. AEs remained manageable, although a close liver surveillance is advised. CTC count appears as a promising biomarker for prognosis and predicting response to treatment. Our study was a phase 2 clinical trial that exhibited the efficacy and tolerance of a novel androgen-receptor targeting agent (abiraterone acetate plus prednisone) in patients with prostate cancer who experienced rising prostate-specific antigen after radical prostatectomy, in combination with prostate bed radiotherapy. The results also indicated the feasibility and potential value of circulating tumor cell detection, which constitutes a possible advance in managing prostate cancers.

Sections du résumé

BACKGROUND BACKGROUND
The relevance of next-generation hormone therapies and circulating tumor cells (CTCs) are not elucidated in biochemical recurrence after prostatectomy.
OBJECTIVE OBJECTIVE
To evaluate the combination of abiraterone acetate plus prednisone (AAP), prostate bed radiotherapy (PBRT), and goserelin in biochemically relapsing men after prostatectomy, and to investigate the utility of CTCs.
DESIGN, SETTING, AND PARTICIPANTS METHODS
In this single-arm multicenter phase 2 trial, 46 biochemically relapsing men were enrolled between December 2012 and January 2019. The median follow-up was 47 mo.
INTERVENTION METHODS
All patients received AAP 1000 mg daily (but 750 mg during PBRT), salvage PBRT, and goserelin.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS METHODS
The primary outcome was 3-yr biochemical recurrence-free survival (bRFS) when prostate-specific antigen (PSA) levels were ≥0.2 ng/ml. The secondary outcomes included alternative bRFS (alt-bRFS) when PSA levels were ≥0.5 ng/ml and safety assessment. CTC count was assessed.
RESULTS AND LIMITATIONS CONCLUSIONS
The 3-yr bRFS and alt-bRFS were 81.5% (95% confidence interval or CI [66.4-90.3%]) and 95.6% (95% CI [83.5-98.9%]), respectively. The most common acute radiotherapy-related adverse effect (AE; all grades was pollakiuria (41.3%). The most common late AE (all grades) was urinary incontinence (15.2%). Grade 3-4 acute or late radiotherapy-related AEs were scarce. Most frequent AEs nonrelated to radiotherapy were hot flashes (76%), hypertension (63%), and hepatic cytolysis (50%, of which 20% were of grades 3-4). Of the patients, 11% had a CTC count of ≥5, which was correlated with poorer bRFS (p = 0.042) and alt-bRFS (p = 0.008). The association between CTC count and higher rates of relapse was independent of the baseline PSA level and PSA doubling time (p = 0.42 and p = 0.09, respectively). This study was nonrandomized with a limited number of patients, and few clinical events were reported.
CONCLUSIONS CONCLUSIONS
Adding AAP to salvage radiation therapy and goserelin resulted in high bRFS and alt-bRFS. AEs remained manageable, although a close liver surveillance is advised. CTC count appears as a promising biomarker for prognosis and predicting response to treatment.
PATIENT SUMMARY RESULTS
Our study was a phase 2 clinical trial that exhibited the efficacy and tolerance of a novel androgen-receptor targeting agent (abiraterone acetate plus prednisone) in patients with prostate cancer who experienced rising prostate-specific antigen after radical prostatectomy, in combination with prostate bed radiotherapy. The results also indicated the feasibility and potential value of circulating tumor cell detection, which constitutes a possible advance in managing prostate cancers.

Identifiants

pubmed: 38734543
pii: S2588-9311(24)00108-1
doi: 10.1016/j.euo.2024.04.014
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Loic Ah-Thiane (L)

Department of Radiotherapy, ICO Rene Gauducheau, St-Herblain, France.

Loic Campion (L)

Department of Biostatistics, ICO Rene Gauducheau, St-Herblain, France.

Nedjla Allouache (N)

Department of Radiotherapy, Francois Baclesse Center, Caen, France.

Emmanuel Meyer (E)

Department of Radiotherapy, Francois Baclesse Center, Caen, France.

Pascal Pommier (P)

Department of Radiotherapy, Leon Berard Center, Lyon, France.

Nathalie Mesgouez-Nebout (N)

Department of Radiotherapy, ICO Paul Papin, Angers, France.

Anne-Agathe Serre (AA)

Department of Radiotherapy, Leon Berard Center, Lyon, France.

Gilles Créhange (G)

Department of Radiotherapy, Georges Francois Leclerc Center, Dijon, France.

Valentine Guimas (V)

Department of Radiotherapy, ICO Rene Gauducheau, St-Herblain, France.

Emmanuel Rio (E)

Department of Radiotherapy, ICO Rene Gauducheau, St-Herblain, France.

Paul Sargos (P)

Department of Radiotherapy, Bergonie Institute, Bordeaux, France.

Sylvain Ladoire (S)

Department of Radiotherapy, Georges Francois Leclerc Center, Dijon, France.

Céline Mahier Ait Oukhatar (C)

Groupe des Essais Précoces, Unicancer, Paris, France.

Stéphane Supiot (S)

Department of Radiotherapy, ICO Rene Gauducheau, St-Herblain, France; Inserm UMR1232, CNRS ERL 6001, Nantes University, Nantes, France. Electronic address: Stephane.Supiot@ico.unicancer.fr.

Classifications MeSH