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Efficacy and safety of All-site Radiation therapy and Standard Of Care Therapy with or without Docetaxel for GG5 metastatic Prostate Cancer

Efficacy and safety of All-site Radiation therapy and Standard Of Care Therapy with or without Docetaxel for GG5 metastatic Prostate Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098583
Enrollment
Unknown
Registered
2025-03-11
Start date
2025-03-11
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Prostate cancer

Interventions

Androgen deprivation therapy + novel hormonal therapy + all-site radiation therapy + docetaxel group (Androgen deprivation therapy + novel hormonal therapy + all-site radiation therapy + docetaxel che
Androgen deprivation therapy + novel hormonal therapy + all-site radiation therapy group (Androgen deprivation therapy + novel hormonal therapy + all-site radiation therapy):None

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Initial puncture pathology or postoperative pathology confirms GS 9-10 points. 2.Initial diagnosis or postoperative treatment without adjuvant ADT with complete imaging confirming the occurrence of distant metastases. 3.The treatment regimen was radiotherapy + ADT ± novel hormonal therapy ± chemotherapy. The radiotherapy regimen included all-site radiotherapy for oligometastatic subjects ( 12 months. 5.Age >= 18 years. 6.KPS >= 80. 7.White blood cells >= 3.5 x 10^9/l, neutrophils >= 1.5 x 10^9/l, platelets = 100.0 x 10^9/l, haemoglobin >= 90g/l. 8.Subject informed consent.

Exclusion criteria

Exclusion criteria: 1.Previous history of malignant tumors (except for tumors that have been cured for more than 5 years). 2.Previous abdominal radiotherapy. 3.Weight loss >10% in 6 months. 4.Persons with pre-existing or coexisting hemorrhagic disorders. 5.Presence of active infection. 6.Clinically significant cardiac disease (eg. Medically controlled hypertension, unstable colic, New York Heart Association (NYHA) class = II congestive heart failure, unstable symptomatic arrhythmia, or class = II peripheral vascular disease). 7.Psychological, family, social, and other factors leading to uninformed consent.

Design outcomes

Primary

MeasureTime frame
Overall survival;radiographic Progression-Free Survival;

Secondary

MeasureTime frame
Prostate Cancer-Specific Survival;PSA progression-free survival;time to new anti-cancer treatment;castration-resistant prostate cancer (CRPC)-free survival;skeletal event-free survival;urinary symptom deterioration-free survival;Functional Assessment of Prostate Cancer Therapy;

Countries

China

Contacts

Public ContactXianshu Gao

Peking University First Hospital

gao7777@139.com+86 10 83575239

Outcome results

None listed

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