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Detection of aberrant androgen receptor transcripts in circulating tumour cells as a predictor of resistance to AR- directed treatment in patients with castration-resistant prostate cancer.

Detection of aberrant androgen receptor transcripts in circulating tumour cells as a predictor of resistance to AR- directed treatment in patients with castration-resistant prostate cancer. - Detection of AR splice variants in CTC of men with CRPC.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42793
Enrollment
15
Registered
2015-08-06
Start date
2015-05-01
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

castration-resistent prostate cancer progression during hormonal treatment

Interventions

None listed

Sponsors

Universiteit Antwerpen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

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

MeasureTime 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

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)