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Phase II Trial Evaluating Olaparib Maintenance in Patients with Metastatic Castration-Resistant Prostate Cancer Responsive or Stabilized on Docetaxel Treatment: SOGUG-IMANOL Study

Authors :
María José Juan Fita
Urbano Anido Herranz
María José Mendez-Vidal
Regina Gironés-Sarrió
José Muñoz-Langa
Juan Sepúlveda-Sánchez
Begoña Mellado
Carlos Alvarez-Fernandez
Lucía Heras López
José Antonio López-Guerrero
Zaida García-Casado
Ana Calatrava
Miguel Ángel Climent
Source :
Cancers, Vol 15, Iss 21, p 5223 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

The SOGUG-IMANOL trial was a phase 2, uncontrolled, Spanish multicenter study to assess the effect of maintenance treatment with olaparib on radiographic progression-free survival (PFS) in patients with metastatic castration-resistant prostate cancer (mCRPC) who achieved partial or complete response or disease stabilization on docetaxel treatment and had a documented germline/somatic mutation in any of the homologous recombination repair (HRR) genes. Patients received olaparib 300 mg orally twice daily. From the screened population (n = 134), 26 (19.4%) somatic mutations were found, and 14 patients were included in the study. The median radiographic PFS was 11.1 (95%CI, 5.7 to 16.5) months. The median PSA-PFS was 3.5 (95%CI, 1.0 to 6.0) months, and the median clinical PFS was 14.7 (95%CI, 1.8 to 27.5 months). Clinical benefit was observed in 12 patients (85.7%, 95%CI 67.4% to 100%), including two patients with partial response and 10 with stable disease. Six patients reported grade 3–5 adverse events: asthenia (n = 3), anemia (n = 2) and neutropenia (n = 1). In this setting, olaparib has been shown to be an efficacious maintenance treatment in terms of radiographic PFS and clinical benefit, becoming a therapeutic option for some patients harboring an HRR gene mutation and in scenarios where further investigation is needed.

Details

Language :
English
ISSN :
20726694
Volume :
15
Issue :
21
Database :
Directory of Open Access Journals
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
edsdoj.5e259639d464429b8fe5a204593ff25
Document Type :
article
Full Text :
https://doi.org/10.3390/cancers15215223