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Clinical Trials/NCT03235557
NCT03235557
Completed
Not Applicable

Robotic Radiation Treatment of Prostate Cancer Patients Aged 70 y or More

Centre Francois Baclesse, Luxembourg1 site in 1 country150 target enrollmentOctober 2014
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Centre Francois Baclesse, Luxembourg
Enrollment
150
Locations
1
Primary Endpoint
Acute and late toxicity (Using the CTCAEv4)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Robotic Stereotactic Radiation treatment of prostatic adenocarcinoma of the elderly.

Inclusion criteria : T1-T3b, MRI pelvic nodes negative, M0, any Gleason Score, PSA (Prostate Specific Antigen) <30ng/ml.

Dose : 36.25 Gy in 5 fractions, in 10 days, considering CAPRA Scores≤5 AND 37.5 Gy in 5 fractions, in 10 days, considering CAPRA Scores>5.

Primary objective : acute and late toxicity evaluation at 36 months. Secondary objectives : PSA and MRI response.

Detailed Description

Robotic Stereotactic Radiation treatment of prostatic adenocarcinoma of the elderly. Rationale : Half of the prostatic adenocarcinoma are diagnosed in the elderly but until now curative treatments were not proven to increase overall survival rates. Therefore, very short, comfortable and safe treatments have to be designed to increase the pelvic control of the disease. Moreover, the alpha/beta ratio of the disease ≤3Gray is in favour of using hypofractionation schemes. Primary objective : acute and late toxicity evaluation at 36 months. Secondary objectives : PSA and MRI response and quality of life evaluation. Inclusion criteria : T1-T3b, MRI pelvic nodes negative, M0, any Gleason Score, PSA\<30ng/ml. Dose : 36.25 Gray in 5 fractions, in 10 days, considering CAPRA Score≤5 AND 37.5 Gray in 5 fractions, in 10 days, considering CAPRA Scores\>5. Doses to the Organs At Risk (OAR) : Rectum wall : V36.25\<2%, V27\<20%, V23\<30%, V20\<35%. Bladder wall : V36.25\<2%, V27\<20%, V20\<35%. Considering specifically the prescription of 37.5 Gray, the rectum and bladder wall: V37.5\<2%. Anytime, hot spots of 105 % of the prescription dose must avoid the urethra. Evaluation criteria : CTCAEV4 (Common Toxicity Criteria for Adverse Events, version4), PSA, multiparametric MRI, IPSS (International Prostate Score Symptom) and IIEF5 (International Index of Erectile Function). Methodolgy : this is a three step prospective, observational study of 20 patients each step. Before moving to the next step, the severe acute or late toxicity at a median follow-up of 1 year must remain below 5% each.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
December 2021
Last Updated
3 years ago
Study Type
Observational
Sex
Male

Investigators

Sponsor
Centre Francois Baclesse, Luxembourg
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • MRI pelvic nodes negative,
  • any Gleason Score,
  • PSA\<30ng/ml,
  • WHO (World Health Organisation) score\<2, IPSS≤15,
  • maximal urinary flow rate ≥15ml/s,
  • mean urinary flow rate ≥5ml/s,
  • multiparametric prostatic and pelvis MRI

Exclusion Criteria

  • Prostatic volume \> 100cc,
  • TURP (transurethral prostatectomy) \<3 y,
  • any recurrent prostatitis within the last 3 years,
  • collagenose diseases,
  • ulcero-haemorrhagic rectocolitis or
  • crohn diseases

Outcomes

Primary Outcomes

Acute and late toxicity (Using the CTCAEv4)

Time Frame: During 36 months after treatment

Using the CTCAEv4

Secondary Outcomes

  • Birads score evaluation(at 36 months)
  • PSA evaluation(at 4 and 6 months, than every 6 months for 3 years)
  • Digital rectal exam(at 6, 12, 24 and 36 months)
  • IIEF5 evaluation(at 12, 24 and 36 months)
  • IPSS evaluation(at 12, 24 and 36 months)

Study Sites (1)

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