castration-resistent prostate cancer progression during hormonal treatment
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Willing and able to provide written informed consent 2. Male and age >= 18 years 3. Histologically or cytologically confirmed adenocarcinoma of the prostate 4. Patients eligible to receive enzalutamide or abiraterone acetate as judged by the treating physician 5. Patients with or without prior chemotherapy regimens
Exclusion criteria
Exclusion criteria: 1. Serious or uncontrolled co-existent non-malignant disease, including active and uncontrolled infection. 2. Not willing to comply with the procedural requirements (extra blood draw) of this protocol. 3. Any criteria which renders patients ineligible for new AR-directed therapy (i.e. abiraterone acetate, enzalutamide).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The determination of the clinical relevance for the presence or absence of androgen receptor splice variants in circulating tumour cells from patients with CRPC (with or without previous taxane chemotherapy) is the primary endpoint of this study. | — |
Countries
Netherlands