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A prospective study for the exploration of role of genomic alterations in the prediction of drug efficacy and drug resistance in patients with metastatic castration resistant prostate cancer receiving abiraterone and docetaxel

A prospective study for the exploration of role of genomic alterations in the prediction of drug efficacy and drug resistance in patients with metastatic castration resistant prostate cancer receiving abiraterone and docetaxel

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035645
Enrollment
Unknown
Registered
2020-08-15
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

prostate cancer

Interventions

A:New endocrine therapy followed by chemotherapy
B:Chemotherapy followed by new endocrine therapy

Sponsors

Fudan University Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Male; 2. Aged 18 to 80 years; 3. Histologically or cytologically confirmed adenocarcinoma of prostate; 4. Confirmed metastatic disease by conventional imaging and Diagnosed as metastatic castration-resistant prostate cancer according to the EAU guideline (2020 verision); 5. Not receiving the same new hormone therapy; 6. ECOG 0 - 2; 7. Estimated life expectancy >1 years; 7. Willing and able to provide informed consent; 8. Treatment and follow-up could be arranged.

Exclusion criteria

Exclusion criteria: 1. Previous treatment to primary lesion of prostate and metastatic lesions including radical prostatectomy, radical radiotherapy and radiotherapy of metastatic sites; 2. History of another cancer (except for basal cell carcinoma or other cancers cured for over 5 years); 3. Other severe disease, such as unstable heart disease, myocardial infarction within 6 months before enrollment, NYHA 3-4, uncontrolled hypertension after treatment, severe neural or mental disorder, uncontrolled active infection, acute gastric ulcer, hypercalcemia and COPD requiring hospitalization; 4. Enrolled in another trial before; 5. Not suitable for enrollment accouding to the researchers view.

Design outcomes

Secondary

MeasureTime frame
overall survival;PSA progression free survival;

Primary

MeasureTime frame
Progression free survival;

Countries

China

Contacts

Public ContactDingwei Ye

Fudan University Shanghai Cancer Center

Dwye.shca@gmail.com+86 021-64175590

Outcome results

None listed

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