Clinical Trials Directory

Trials / Terminated

TerminatedNCT01981707

F-choline PET in Early Response Assessment for Castration Resistant Prostatic Cancer

F-choline PET in Early Response Assessment for Castration Resistant Prostatic Cancer Treated by Abiraterone Acetate or Enzalutamide

Status
Terminated
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
12 (actual)
Sponsor
University Hospital, Grenoble · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

Until today no current diagnostic tool exists to identify an early objective response when patients with castration-resistant prostate cancer were treated by abiraterone acetate or enzalutamide. According to the Prostate Cancer Working Group, the investigators have to wait 12 weeks before the first evaluation. To know soon that the treatment is effective will be decisive for the oncologist, even more in palliative situation where second effects can't be imposed to patients. In post-docetaxel, the F-choline PET-CT could be used to assess the response of this new therapy. Moreover, the investigators suppose that we can assess an early stage if there is an objective therapeutic response, at 6 weeks of treatment, in order to avoid unnecessarily and expansive treatment. The aim of this study is to assess if it is possible to determine early (6 weeks of treatment)if a F-choline PET-CT could predict the response to abiraterone acetate or enzalutamide in post-docetaxel.

Conditions

Interventions

TypeNameDescription
DEVICEF-Choline-PET

Timeline

Start date
2013-12-01
Primary completion
2015-12-01
Completion
2016-03-01
First posted
2013-11-11
Last updated
2016-04-28

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01981707. Inclusion in this directory is not an endorsement.