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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05430737
Other study ID # SBRT-PCa-001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 30, 2022
Est. completion date June 30, 2025

Study information

Verified date June 2022
Source West China Hospital
Contact xin wang, PhD/MD
Phone +86 28 85423609
Email wangxin213@sina.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Stereotactic body radiotherapy (SBRT) has emerged as an effective and safe treatment for low and intermediate-risk prostate cancer(PCa). However, there is no study that has investigated the effectiveness and safety of SBRT with pelvic radiation and gross target volume(GTV) boost for high-risk prostate cancer patients yet. The investigators designed a phase II clinical study of SBRT with pelvic radiation and GTV boost based on mpMRI in patients with high-risk prostate cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 30, 2025
Est. primary completion date June 30, 2025
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria: - 18 years or older - pathologically confirmed high-risk (T3a or Gleason score = 8 or a PSA > 20 ng/ml) prostate cancer - a WHO performance status 0-1 - history of neoadjuvant androgen deprivation therapy(ADT) within 6 months before enrollment - Patients with pelvic positive lymph node were also included in our study Exclusion Criteria: - distant metastasis - history of neoadjuvant ADT over 6 months before enrollment - history of definitive treatment for prostate cancer such as radical prostatectomy - history of pelvic irradiation; prostate volume=100 cm3

Study Design


Intervention

Radiation:
stereotactic body radiotherapy
The radiation dose to the primary tumor was 40 or 45 Gy in five fractions according to the clinical determination of the radiologist. The dose to the positive lymph nodes and the prostate and seminal vesicles was 37.5Gy in five fraction. And internal iliac, external iliac, obturator, and presacral pelvic drainage regions received 25 Gy/5f, simultaneously. The treatment was delivered every other day. The volumetric modulated arc radiotherapy (VMAT) or intensity-modulated radiotherapy (IMRT) was used to complete treatment. Image-guided radiotherapy(IGRT) was performed for every treatment.

Locations

Country Name City State
China China, SiChuan Chengdu Sichuan

Sponsors (1)

Lead Sponsor Collaborator
West China Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary biochemical relapse-free survival 2-years biochemical relapse-free survival three months
Secondary the incidence rate of acute toxicity the incidence rate of toxicity in 90 days every week
Secondary the incidence rate of late toxicity the incidence rate of toxicity after 90 days three months
Secondary patient-reported quality of life patient-reported quality of life using European Organization for Research and Treatment of Cancer Quality-of-Life-Questionnaire-Core-30(EORTC QLQ C30) .The The minimum and maximum values of EORTC QLQ C30 are 0 and 100,respectively.Higher scores for functional and overall health areas of EORTC QLQ C30 indicate better functional status and quality of life, and higher scores for symptom areas indicate more symptoms or problems. three months
Secondary symptom score Symptom score using the International Prostatic System Score (IPSS) .The minimum and maximum values of IPSS are 0 and 35,respectively.A higher score of IPSS means a poorer quality of life. three months
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