PROceed is a multisite, prospective, observational study that describes the real-world use and clinical experience of mCRPC patients treated with the combination of olaparib and abiraterone in the mCRPC setting. Clinical outcomes will be assessed in patients who are either NHA-naive or NHA-exposed prior to initiating olaparib + abiraterone treatment, respectively. Patient demographic and clinical characteristics, as well as treatment received prior and subsequent to olaparib + abiraterone, will also be described. The study plans to enroll patients for a maximum of 2 years and follow up patients from initiation of olaparib until 1 year post last patient in.
Willing and able to provide written informed consent;
18 years of age and above;
Documented histopathology or cytopathology of PCa, adenocarcinoma;
Confirmed as mCRPC;
Patients participating in a clinical trial with an investigational prostate cancer treatment within 30 days prior to olaparib initiation
AstraZeneca
Lead sponsor
Merck Sharp & Dohme LLC
Collaborator