Prostate Cancer
Conditions
Keywords
Prostate cancer, proton radiotherapy, photon radiotherapy
Brief summary
ProtoChoice-P is a prospective multicenter trial to evaluate proton therapy in patients suffering from prostate cancer. Primary aim of the study is a decrease of moderate or severe genito-urinary or intestinal side effects (Common Terminology Criteria for Adverse Events (CTCAE) 4.0 grade 2 or higher) by the use of proton therapy. Secondary endpoints contain assessment of quality of life, biochemical recurrence and recurrence free survival as well as overall survival and economic comparison between photon and proton therapy.
Detailed description
The hypothesis of the study is a 7.5% decrease of combined genito-urinary and intestinal side effects from 15% with photon therapy to 7.5% by the use of protons. With an alpha of 0.05 and 80% power it is therefore necessary to treat 131 patients with protons to detect such difference. With an estimated drop-out rate of 10% 146 patients have to be recruited to the proton arm. As randomization to photon or proton therapy is not possible in a multicenter setting with only few proton facilities available patients treated with photons will be prospectively matched to their proton counterparts. Stratification criteria will include: Age, high dose volume, androgen deprivation, history of surgery, obstructive disease, increased risk for rectal bleeding, socio-economic criteria and use of rectal balloon during radiotherapy. Comparison of the primary endpoint will be restricted to patients without irradiation of lymphatic drainage.
Interventions
RADIATIONRadiotherapy with protons
RADIATIONRadiotherapy with photons
Sponsors
Technische Universität Dresden
German Consortium for Translational Cancer Research
National Center for Radiation Research in Oncology Dresden/Heidelberg
Radiation Oncology Working Group of the German Cancer Society
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* life expectancy ≥ 10 years * adenocarcinoma of the prostate confirmed by punch biopsy * locally limited to locally advanced adenocarcinomas without evidence of distant metastases i.e. T1-3b N0-1 M0 * stage-related indicated neoadjuvant / adjuvant androgen deprivation possible (neoadjuvant ≤ 6 months) * good general condition (ECOG performance status 0 - 1) * marker seed implantation before irradiation (optional) or possibility of Image-guided Radiation Therapy (IGRT) by CT * adequate compliance for follow-up * written informed consent
Exclusion criteria
* distant metastases * previous radiotherapy of the lesser pelvis * previous or concomitant other malignant disease except when there is no impact on treatment or follow-up of the prostate cancer * participation in another clinical study, if it's excluded by the study protocols
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cumulative incidence of moderate/ severe side effects | after 2 years ( measured from the first day of treatment) | ≥ grade 2 by CTCAE combined for genito-urinary and gastrointestinal side effects |
Countries
Germany
Contacts
STUDY_CHAIRTobias Hölscher, Dr.
University Hospital C. G. Carus Dresden, Departm. of Radiation Therapy and Radiation Oncology
Outcome results
None listed