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Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies (PAROS)

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Hypofractionated radiotherapy with photons
Hypofractionated radiotherapy with protons
Normofractionated radiotherapy with photons
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • histology-proven prostate cancer with Gleason Score and PSA-value;
  • indication for prostate bed irradiation (adjuvant/ salvage) after prostatectomy;
  • Karnofsky-Index ≥ 70%
  • age ≥ 18 years

Exclusion Criteria:

  • androgen deprivation therapy
  • lymphatic spread
  • macroscopic tumor/ R2
  • stage IV (M1)
  • previous irradiation

Sites / Locations

  • University Hospital HeidelbergRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

70.0/ 2.0 Gray (RBE)

57.0/ 3.0 Gray (RBE)

57.0/ 3.0 (RBE)

Arm Description

Normofractionated radiotherapy with photons (70.0/ 2.0 Gray)

Hypofractionated radiotherapy with photons (57.0/ 3.0 Gray)

Hypofractionated radiotherapy with protons (57.0/ 3.0 Gray relative biological effectiveness [RBE]).

Outcomes

Primary Outcome Measures

Quality of life (prostate-associated, 12 weeks vs baseline)
The primary objective of the present trial is to show a Change in the bowel symptoms according to scores on the EORTC QLQ-PR25 questionaire after proton therapy compared to photon irradiation (week 12 vs. baseline).

Secondary Outcome Measures

biochemical progression-free survival (bPFS)
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to biochemical progression-free survival (bPFS)
overall survival (OS)
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to overall survival (OS)
Toxicity acc. to NCI CTCAE V 5.0 after 2 and 5 years
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to toxicity
Quality of life (general and prostate-associated, 2 years and 5 years vs. baseline)
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to changes in the scores of quality of life based on the EORTC QLQ-C30 questionaire
Quality of life (general and prostate-associated, 2 years and 5 years vs. baseline)
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to changes in the scores of quality of life based on the EORTC QLQ-PR25 questionaire

Full Information

First Posted
January 7, 2019
Last Updated
November 2, 2022
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT04083937
Brief Title
Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies
Acronym
PAROS
Official Title
Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 12, 2018 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
January 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
As the most common male carcinoma, prostate cancer is a major tumor entity in oncology. In addition to definitive radiotherapy, surgical procedure is considered to be an oncologically equivalent therapeutic alternative for non-metastatic malignancies in the primary setting. However, a subsequent radiotherapy of the prostate bed is often necessary, which takes place as an "adjuvant" treatment immediately after surgery or in the course of a repeated increase in PSA and usually extends over several weeks. For the primary situation (without previous surgery), several randomized phase III clinical trials have shown that it is possible to shorten radiotherapy by increasing the single dose (called hypofractionation). In the context of two prospective Phase II studies, which were carried out in Heidelberg, it has since been shown that hypofractionation with both photons and protons is safe and feasible even in the postoperative situation. The current, prospective and randomized PAROS study is now intended to demonstrate a multicentric phase III study as an improvement in the quality of life caused by rectum toxicity (primary endpoint) by the use of protons. The oncological non-inferiority of hypofractionated radiotherapy after surgery is a secondary endpoint.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
897 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
70.0/ 2.0 Gray (RBE)
Arm Type
Active Comparator
Arm Description
Normofractionated radiotherapy with photons (70.0/ 2.0 Gray)
Arm Title
57.0/ 3.0 Gray (RBE)
Arm Type
Experimental
Arm Description
Hypofractionated radiotherapy with photons (57.0/ 3.0 Gray)
Arm Title
57.0/ 3.0 (RBE)
Arm Type
Experimental
Arm Description
Hypofractionated radiotherapy with protons (57.0/ 3.0 Gray relative biological effectiveness [RBE]).
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated radiotherapy with photons
Intervention Description
hypofractionated radiotherapy with photons (total dose 57.0 Gray in 19 fractions)
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated radiotherapy with protons
Intervention Description
hypofractionated radiotherapy with protons (total dose 57.0 Gray relative biological effectiveness (RBE) in 19 fractions)
Intervention Type
Radiation
Intervention Name(s)
Normofractionated radiotherapy with photons
Intervention Description
normofractionated radiotherapy with photons (total dose 70.0 Gray in 35 fractions)
Primary Outcome Measure Information:
Title
Quality of life (prostate-associated, 12 weeks vs baseline)
Description
The primary objective of the present trial is to show a Change in the bowel symptoms according to scores on the EORTC QLQ-PR25 questionaire after proton therapy compared to photon irradiation (week 12 vs. baseline).
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
biochemical progression-free survival (bPFS)
Description
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to biochemical progression-free survival (bPFS)
Time Frame
5 years after baseline
Title
overall survival (OS)
Description
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to overall survival (OS)
Time Frame
5 years after baseline
Title
Toxicity acc. to NCI CTCAE V 5.0 after 2 and 5 years
Description
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to toxicity
Time Frame
2 and 5 years after baseline
Title
Quality of life (general and prostate-associated, 2 years and 5 years vs. baseline)
Description
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to changes in the scores of quality of life based on the EORTC QLQ-C30 questionaire
Time Frame
2 and 5 years after baseline
Title
Quality of life (general and prostate-associated, 2 years and 5 years vs. baseline)
Description
non-inferiority of hypofractionated radiotherapy compared to normofractionated radiotherapy with regard to changes in the scores of quality of life based on the EORTC QLQ-PR25 questionaire
Time Frame
2 and 5 years after baseline

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histology-proven prostate cancer with Gleason Score and PSA-value; indication for prostate bed irradiation (adjuvant/ salvage) after prostatectomy; Karnofsky-Index ≥ 70% age ≥ 18 years Exclusion Criteria: androgen deprivation therapy lymphatic spread macroscopic tumor/ R2 stage IV (M1) previous irradiation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juergen Debus
Phone
06221 56 8201
Email
juergen.debus@med.uni-heidelberg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juergen Debus
Organizational Affiliation
University Hospital Heidelberg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Heidelberg
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juergen Debus
Phone
06221 56 8201
Email
juergen.debus@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Adriane Hommertgen
Phone
06221 56 8201
Email
adriane.hommertgen@med.uni-heidelberg.de

12. IPD Sharing Statement

Learn more about this trial

Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies

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