FLAME: Investigate the Benefit of a Focal Lesion Ablative Microboost in Prostate Cancer

Phase

Condition

Prostate Cancer

Urologic Cancer

Prostate Cancer, Early, Recurrent

Treatment

N/A

Clinical Study ID

NCT01168479

UMCU-FLAME

Ages > 18
Male

Study Summary

Rationale: Dose escalation in external-beam irradiation has proven to benefit outcome in local prostate cancer. Randomized trials were performed up to doses of 78 Gy in 2 Gy fractions. Nevertheless, the five-year biochemical relapse rate still was approximately 35% in the high-dose arm. Therefore further dose escalation seems to be required. A feasibility study up to appr. 85 Gy on the entire prostate has already been performed and showed acceptable toxicity when combined with adequate position verification. Higher doses to the entire prostate are expected to increase severe toxicity. As local recurrences only occur at the site of the primary macroscopic tumour area the next step in increasing the dose should be an ablative boost to the macroscopic tumour alone, while electively irradiating the rest of the prostate to the current gold standard dose. Feasibility of this approach has been shown for an ablative dose of 95 Gy to the macroscopic tumour within the prostate.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Prostate cancer patients scheduled for external beam radiotherapy using IMRT andfiducial marker-based position verification
Intermediate and high risk prostate cancer, defined by Ash et al. 2000, namely:
One or more factors: T2, or Gleasonscore >7, or iPSA > 10 ng/mL
WHO score 0-2

Exclusion

Exclusion Criteria:

Low risk prostate cancer, defined by Ash et al. 2000
World Heath Organisation (WHO) score >2
International Prostate Symptom Score (IPSS) >20
If for any patient related reason an MRI cannot be performed
If anticoagulation cannot be stopped temporarily regarding the implant of fiducialmarkers
Previous prostatectomy (except from Trans Urethral Prostatectomy (TURP))
TURP within 3 months from start treatment
Previous pelvic irradiation

Study Design

September 01, 2009

January 31, 2016

Study Description

Objective:

Primary study objective: To demonstrate the superiority of the ablative microboost dose schedule regarding 5-year biochemical no evidence of disease rate compared to the current standard of care.
Secondary study objectives: Establish and compare the rates of treatment-related toxicity, quality of life and disease-free survival.

Study design: Single blind prospective randomized controlled phase III trial.

Study population: Patients with intermediate or high risk adenocarcinoma of the prostate. Intermediate or high risk is defined according to the Ash et al. 2000 criteria as:

One (intermediate-risk) or more (high-risk) factors: T2, or Gleasonscore=7, or iPSA 10-20 ng/mL
One or more (high-risk) factors: T3, or Gleasonscore >7, or iPSA >20 ng/mL

Intervention: The standard arm receives the current gold standard, namely 77Gy to the prostate in 35 fractions of 2.2 Gy, 5 times per week. In the experimental arm patients receive in addition to the current gold standard of 77 Gy to the prostate an integrated boost to the macroscopically visible tumour to reach a total dose of 95 Gy in 35 fractions of 2.7 Gy, 5 times per week.

Main study endpoint: To decrease the five-year biochemical relapse rate with at least 10%.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

Patients will have to fill in a quality of life questionnaire before and after the radiotherapy treatments. The risk associated with the increased dose to the macroscopic tumour is an increase of toxicity and a reduction of quality of life.

Connect with a study center

University Hospitals Leuven
Leuven, Vlaans-Brabant 3000
Belgium
Site Not Available
Radboud UMC
Nijmegen, Gelderland 6500HB
Netherlands
Site Not Available
NKI-AvL
Amsterdam, Noord-Holland 1066CX
Netherlands
Site Not Available
University Medical Center Utrecht
Utrecht, 3584CX
Netherlands
Site Not Available

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