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OpenTrials
Completed

NCT Number: NCT00201916

Shorter Radiation Schedule for the Treatment of Prostate Cancer

To improve the management of patients with early stage prostate cancer.

Completed

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Key information

Sex eligibility

Male

Study type

Interventional

Phase

Phase 3

Primary location

B.C. Cancer Agency - Fraser Valley Cancer Centre, Surrey, British Columbia, Canada

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About this study

To compare the efficacy of a shorter radiation fractionation schedule to the prostate (5250 cGy/20 fractions over 28 days) with a conventional schedule (6600 cGy/33 fractions over 45 days) in men receiving radiotherapy for Stage T1a moderately or poorly differentiated, or T1b, T1c, or T2 prostate cancer. The primary outcome is local control in the prostate and secondary outcomes include toxicity, disease free survival, survival, quality of life and economics.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • histologic diagnosis of adenocarcinoma of the prostate with no evidence of metastatic disease to the nodes, bone or lung
  • stage T1a moderately or poorly differentiated, T1b, T1c or T2 by the current UICC-TNM classification

Exclusion criteria

  • PSA > 40 mcg/L
  • previous therapy for carcinoma of the prostate other than biopsy or TURP, including patients previously on hormone therapy for treatment of their prostate cancer
  • prior or active malignancy other than non-melanoma skin cancer; or colon or thyroid cancer treated a minimum of five years prior to study entry and presumed cured
  • simulated volume exceeds 1000 cm3
  • previous pelvic radiotherapy
  • inflammatory bowel disease
  • serious non-malignant disease which would preclude radiotherapy or surgical biopsy
  • geographic inaccessibility for follow-up
  • psychiatric or addictive disorder which would preclude obtaining informed consent or adherence to protocol
  • unable to commence radiation therapy within 26 weeks of the date of last prostatic biopsy
  • failure to give informed consent to participate in the study

Treatment and study plan

5250 cGy/20 fractions over 28 days

Procedure

see above

Other names: short fractionation schedule

6600 cGy/33 fractions over 45 days

Procedure

see above

Other names: standard

Primary outcomes

  1. time to PSA failure

    Time frame: 10 years

Secondary outcomes

  1. positive biopsy at two years post radiation

    Time frame: see above

  2. disease free survival

    Time frame: 10 years

  3. toxicity

    Time frame: 10 years

  4. quality of life

    Time frame: 6 years

  5. economic

    Time frame: 10 years

Sponsors and collaborators

Lead sponsor

Ontario Clinical Oncology Group (OCOG)

Other

Collaborators

  • NCIC Clinical Trials Group

Registry information

Official study title

A Randomized Trial of a Shorter Radiation Fractionation Schedule for the Treatment of Localized Prostate Cancer

Important dates

Study start
1995
Primary completion
2008
Study completion
2009
First posted
Sep 20, 2005
Registry last updated
Aug 17, 2010

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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