World Journal of Oncology, ISSN 1920-4531 print, 1920-454X online, Open Access
Article copyright, the authors; Journal compilation copyright, World J Oncol and Elmer Press Inc
Journal website http://www.wjon.org

Case Report

Volume 9, Number 4, August 2018, pages 119-122


DNA Damage Repair (DDR) Mutations and the Utility of High-Risk Genetics Clinics in Metastatic Castration-Refractory Prostate Cancer (mCRPC)

Table

Table 1. Completed and Ongoing Phase 2/3 Clinical Trials Evaluating PARP Inhibitors in Men With Metastatic Castration-Refractory Prostate Cancer
 
TrialArmsPhasePopulationnPrimary endpointEstimated primary completion date
AA: abiraterone acetate plus prednisone; enza: enzalutamide; mCRPC: metastatic castration-refractory prostate cancer; rPFS: radiographic progression-free survival; DDR: DNA damage repair; ORR: objective response rate; PSA: prostate-specific antigen; PFS: progression-free survival. Primary completion date: the date on which the last participant in the clinical study was examined or received an intervention to collect final data for the primary outcome measure.
PROfound (NCT02987543)Olaparib
AA or enza
3mCRPC340rPFS2020
Talapro-2 (NCT03395197)Talazoparib + enza
Enza + placebo
3mCRPC with DDR deficiency352rPFS2022
TRITON3 (NCT02975934)Rucaparib
AA, enza or docetaxel
3mCRPC with DDR deficiency400rPFS2022
NCT02893917Olaparib + cediranib
Olaparib
2mCRPC90rPFS2019
BRCAAway (NCT03012321)AA + olaparib2mCRPC with DDR deficiency70PFS2021
Olaparib
AA
Completed trials
TrialArmsPhasePopulationnORRPFS
NCI 9012 (NCT01576172)AA + veliparib
AA
2mCRPC14872.4%14.5 m (DDR+) versus 8.0 m (WT)
TOPARP-A (NCT01682772)Olaparib2mCRPC8933%9.8 m (DDR+) versus 2.7 m (WT)