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A cohort study about the role of AR - V7 in evaluating the prognosis of prostate cancer receiving androgen deprivation therapy

A cohort study about the role of AR - V7 in evaluating the prognosis of prostate cancer receiving androgen deprivation therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-POC-16008239
Enrollment
Unknown
Registered
2016-04-07
Start date
2016-04-10
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Prostate cancer

Interventions

AR-V7positive:None
AR-V7negative:None

Sponsors

Department of Urology Laboratory, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients who are diagnosed with metastatic prostate adenocarcinoma and start to receive standard androgen deprivation therapy included medical castration (luteinizing hormone releasing hormone analogs, LHRH-a) or surgical castration (orchiectomy), combined with medical anti androgen (bicalutamide etc.). The adenocarcinoma is confirmed by Immunohistochemistry (IHC) using formalin-fixed paraffin-embedded (FFPE) needle biopsy. Metastatic disease is confirmed by bone scanning.

Exclusion criteria

Exclusion criteria: 1. Patient who has serious heart, lung, liver or kidney disease; 2. Patient who refuses to accept androgen deprivation therapy; 3. Patient who failed to regulate androgen deprivation therapy under the requirements of doctor; 4. Patient whose serum testosterone does not reach castration level (<50ng/dl); 5. In addition to androgen deprivation therapy, patient who undergoes other anti-tumor therapy, including surgery, chemotherapy or radiation therapy; 6. Patient with a history of transurethral resection of prostate or other cancers; 7. Patient with ECOG performance status score larger than 2.

Design outcomes

Primary

MeasureTime frame
AR-V7immuno -histochemistry;progress-free survival;

Secondary

MeasureTime frame
cancer-specific survival;overall survival;PSA response rate;

Countries

China

Contacts

Public ContactYe Zhangqun

Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology

zhangqun_ye@163.com+86 027-83663460

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026