Skip to content

A real-world retrospective study evaluating the ADT combined with docetaxel and darolutamide triple therapy regimen for metastatic prostate cancer(YHCG-006)

A real-world retrospective study evaluating the ADT combined with docetaxel and darolutamide triple therapy regimen for metastatic prostate cancer(YHCG-006)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118253
Enrollment
Unknown
Registered
2026-02-03
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

prostate cancer

Interventions

Triple therapy group(ADT +Docetaxel + Darolutamide):NA

Sponsors

The First Affiliated Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male, > 18 years; 2. Pathologically confirmed prostate adenocarcinoma, with distant metastases proven by bone scan, MRI, CT, or PET. 3. Androgen deprivation therapy before or during darolutamide treatment; 4. Received at least one dose of docetaxel during darolutamide treatment; 5. As a real-world study, it allows subjects to receive local treatments such as surgery and radiotherapy.

Exclusion criteria

Exclusion criteria: 1. Neuroendocrine prostate cancer or small cell prostate cancer; 2. Lack of enough clinical data or lost of follow up; 3. Patients with concurrent cancers at the time of diagnosis of mPC or who have received any anti-cancer therapy for other cancers within 6 months after diagnosis of mPC, except for non-metastatic non-melanoma skin cancer or in situ or benign tumors.

Design outcomes

Primary

MeasureTime frame
PSA response rate;Proportion of PSA<0.2ng/ml;PSA progression time;

Countries

China

Contacts

Public ContactQi Ma

The First Affiliated Hospital of Ningbo University

45112409@qq.com+86 574 8708 9078

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026