Centre Francois Baclesse
Esch-sur-Alzette, 4005, Luxembourg
NCT Number: NCT03235557
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.
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Notify Me70 year and older
Male
Observational
Esch-sur-Alzette, 4005, Luxembourg
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: During 36 months after treatment
Using the CTCAEv4
Time frame: at 4 and 6 months, than every 6 months for 3 years
PSA Dosage
Time frame: at 6, 12, 24 and 36 months
Clinical examination (digital rectal exam)
Time frame: at 36 months
Multiparametric prostatic MRI
Time frame: at 12, 24 and 36 months
IPSS score
Time frame: at 12, 24 and 36 months
IIEF5 score
Centre Francois Baclesse, Luxembourg
Other
Robotic Radiation Treatment of Prostate Cancer Patients Aged 70 y or More
Acronym: ProRobot
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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