Skip to content

A prospective cohort study on the prognosis of androgen deprivation therapy combined with docetaxel chemotherapy in ar-v7 negative high-risk metastatic hormone sensitive prostate cancer

A prospective cohort study on the prognosis of androgen deprivation therapy combined with docetaxel chemotherapy in ar-v7 negative high-risk metastatic hormone sensitive prostate cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060915
Enrollment
Unknown
Registered
2022-06-14
Start date
2022-05-30
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

prostatic cancer

Interventions

High risk metastatic hormone sensitive prostate cancer:NA

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Prostate adenocarcinoma was diagnosed by pathology; (2) High risk metastatic prostate cancer was considered by imaging examination including pmsa-pet and bone scan: Gleason score = 8, there were three or more lesions in bone scan, or there were measurable visceral metastasis except lymph node metastasis; (3) No previous anti-tumor treatment including androgen deprivation therapy; (4) ECOG score = 2; (5) Immunohistochemical ar-v7 staining was positive in prostate cancer; (6) Patients who can tolerate androgen deprivation therapy, docetaxel chemotherapy and abiraterone therapy.

Exclusion criteria

Exclusion criteria: (1) Patients with life expectancy less than 1 year; (2) Patients who have serious mental illness or are unable to cooperate with treatment or follow-up due to other reasons; (3) Patients who fail to treat according to the doctor's instructions; (4) Patients with other neoplastic diseases; (5) Prostate cancer with pathological types other than adenocarcinoma; (6) Patients with severe allergy to gonadotropin releasing hormone (GnRH) analogues; (7) Blood testosterone could not reach castration level (= 50ng/ml) during treatment; (8) Patients receiving immunosuppressive therapy or with immune deficiency diseases; (9) Patients with severe liver function impairment (child Pugh grade C); (10) Patients with severe renal function injury who need long-term dialysis treatment; (11) Patients with severe myelosuppression and severe neutropenia; (12) Participate in other clinical studies from 30 days before enrollment to the completion of this study.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactHua Xu
xuhuawhu@163.com13971051016

Outcome results

None listed

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