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Sequential Therapy with Docetaxel and Abiraterone Acetate in Castration-Resistant Prostate Cancer: Real-World Survival Analysis

Sequential Therapy with Docetaxel and Abiraterone Acetate in Castration-Resistant Prostate Cancer: Real-World Survival Analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260530001
Enrollment
50
Registered
2026-05-30
Start date
2025-11-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

A retrospective study comparing the effective sequencing strategy between abiraterone and docetaxel in metastatic castration - resistant prostate cancer in Ramathibodi Hospital, Thailand. Prostatic Neoplasms, Castration-Resistant, Drug Sequencing, Real-World Evidence

Interventions

Abiraterone acetate was administered as first-line treatment for metastatic CRPC, followed by docetaxel as second-line therapy.,Docetaxel was administered as first-line treatment for metastatic CRPC,
Treatment,Treatment
First line with Abiraterone acetate,First line with Docetaxel

Sponsors

None listed

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult male patients whose age > 18 years old 2. Diagnosed with metastatic castration-resistant prostate cancer (mCRPC) who have received both standard systemic therapies, including abiraterone acetate and/or docetaxel.

Exclusion criteria

Exclusion criteria: 1. Patients with non-adenocarcinoma histology. 2. Patients who have had prior chemotherapy in the hormone-sensitive setting, and receipt of investigational therapies, all of which may confound treatment effects. 3. Patients with baseline central nervous system involvement 4. Patients who were active concurrent with other malignancies. 5. Patients with a limited life expectancy (<3 months) at the initiation of mCRPC treatments.

Design outcomes

Primary

MeasureTime frame
Progression free survival Jan 2015 - Until death or at the end of completion date ( 19 April 2026) Day

Secondary

MeasureTime frame
Prostate-Specific Antigen Response 3, 6, 9, 12 months after treatment Percentage

Countries

Thailand

Contacts

Public ContactPhichai Chansriwong

Ramathibodi Hospital

phichaionco103@gmail.com022011671

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026