ProtoChoice-P: Preference-based Comparative Study on Definitive Radiotherapy of Prostate Cancer With Protons

Sponsor
Technische Universität Dresden (Other)
Overall Status
Recruiting
CT.gov ID
NCT02766686
Collaborator
German Consortium for Translational Cancer Research (Other), National Center for Radiation Research in Oncology Dresden/Heidelberg (Other), Radiation Oncology Working Group of the German Cancer Society (Other)
146
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83
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Radiotherapy with protons
  • Radiation: Radiotherapy with photons
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
146 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Preference-based Comparative Study on Definitive Radiotherapy of Prostate Cancer With Protons in Standard Fractionation and Standard Dosage
Study Start Date :
Sep 1, 2016
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Radiotherapy with protons

Proton radiotherapy 74-80 Gray equivalent (GyE), 2Gy per fraction, 5 fractions peer week

Radiation: Radiotherapy with protons

Active Comparator: Radiotherapy with photons

Photon-Intensity-Modulated Radiation Therapy (IMRT) without lymph drainage vessels, 74-80 Gy, 2Gray (Gy) per fraction, 5 fractions peer week

Radiation: Radiotherapy with photons

Other: Radiotherapy with photons with lymph drainage vessels

Photon-IMRT with lymph drainage vessels, 74-80 Gy, 2Gy per fraction, 5 fractions peer week

Radiation: Radiotherapy with photons

Outcome Measures

Primary Outcome Measures

  1. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Carl Gustav Carus, Department of Radiotherapy and Radiation Oncology Dresden Germany 01307
2 Klinikum rechts der Isar, Technische Universität München Munich Germany 81675
3 Universitätsklinik für Radioonkologie, Universitätsklinikum Tübingen Tubingen Germany 72076

Sponsors and Collaborators

  • 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

Investigators

  • Study Chair: Tobias Hölscher, Dr., University Hospital Carl Gustav Carus, Department of Radiation Therapy and Radiation Oncology, German Consortium for Translational Cancer Research (DKTK)

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tobias Hölscher, Dr. Tobias Hölscher, Technische Universität Dresden
ClinicalTrials.gov Identifier:
NCT02766686
Other Study ID Numbers:
  • STR - ProtoChoice-P - 2015
First Posted:
May 10, 2016
Last Update Posted:
Aug 19, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tobias Hölscher, Dr. Tobias Hölscher, Technische Universität Dresden
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 19, 2021