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Completed

NCT Number: NCT03235557

CyberKnife for Prostate Cancer Patients Aged 70 y or More

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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Key information

Age range

70 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Centre Francois Baclesse

Esch-sur-Alzette, 4005, Luxembourg

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • T1-T3b,
  • MRI pelvic nodes negative,
  • M0,
  • 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

Treatment and study plan

Primary outcomes

  1. Acute and late toxicity (Using the CTCAEv4)

    Time frame: During 36 months after treatment

    Using the CTCAEv4

Secondary outcomes

  1. PSA evaluation

    Time frame: at 4 and 6 months, than every 6 months for 3 years

    PSA Dosage

  2. Digital rectal exam

    Time frame: at 6, 12, 24 and 36 months

    Clinical examination (digital rectal exam)

  3. Birads score evaluation

    Time frame: at 36 months

    Multiparametric prostatic MRI

  4. IPSS evaluation

    Time frame: at 12, 24 and 36 months

    IPSS score

  5. IIEF5 evaluation

    Time frame: at 12, 24 and 36 months

    IIEF5 score

Sponsors and collaborators

Lead sponsor

Centre Francois Baclesse, Luxembourg

Other

Registry information

Official study title

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

Acronym: ProRobot

Important dates

Study start
2014
Primary completion
2018
Study completion
2021
First posted
Aug 1, 2017
Registry last updated
Jun 22, 2022

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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