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Evaluating the Impact of Prostate Only Versus Pelvic Radiation for N+ Prostate Cancer. (PROPER)

Primary Purpose

Prostate Cancer

Status
Terminated
Phase
Phase 3
Locations
Belgium
Study Type
Interventional
Intervention
radiotherapy
Sponsored by
University Hospital, Ghent
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:

  • Histological proven carcinoma of the prostate
  • Positive lymph nodes found on extended pelvic dissection (EPLND) defined as:
  • Removal of the lymphatic tissue in the obturator fossa + along the external iliac vessels + additional complete resection of the lymph nodes (lnn) along, medially and laterally to, the hypogastric vessels
  • If technically feasible: removal of lnn along the common iliac vessels
  • Removal of ≥10 lnn
  • Treatment of the primary tumor by either radical prostatectomy or EBRT
  • Willing to receive androgen deprivation therapy
  • World health organization 0-2
  • Written informed consent

Exclusion Criteria:• >4 positive lnn found on EPLND

  • Prior pelvic irradiation
  • Other primary tumor (except for non-melanoma skin tumors) diagnosed <5 years before enrollment
  • Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule

Sites / Locations

  • Ghent University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Prostate(bed) only

Prostate(bed) and pelvis

Arm Description

external beam radiotherapy limited to the prostate(bed)

external beam radiotherapy to the prostate(bed) and pelvic lymph node regions

Outcomes

Primary Outcome Measures

Assessment of number of participants without clinical relapse
presence of loco(regional) release or distant metastases

Secondary Outcome Measures

Assessment of number of participants experiencing Radiation Therapy Oncology Group toxicity
acute
Assessment of number of participants experiencing Radiation Therapy Oncology Group toxicity
late
Assessment of number of participants with biochemical control
absence of prostate specific antigen relapse

Full Information

First Posted
April 15, 2016
Last Updated
December 23, 2022
Sponsor
University Hospital, Ghent
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1. Study Identification

Unique Protocol Identification Number
NCT02745587
Brief Title
Evaluating the Impact of Prostate Only Versus Pelvic Radiation for N+ Prostate Cancer.
Acronym
PROPER
Official Title
The N+-PROPER Trial: Evaluating the Impact of Prostate Only Versus Pelvic Radiation for N+ Prostate Cancer.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Terminated
Why Stopped
Stopped because of poor accrual in June 2021 after the inclusion of 69 patients
Study Start Date
April 1, 2016 (Actual)
Primary Completion Date
July 1, 2021 (Actual)
Study Completion Date
September 22, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
At least 40% of the patients with prostate cancer (PC) present with positive lymph nodes (N1). The optimal treatment strategy for these patients remains controversial. Although androgen deprivation therapy (ADT) is still often initiated as only treatment, the results are disappointing. Recent studies support the use of more aggressive therapies including external beam radiotherapy (EBRT) and ADT. The retrospective studies supporting the additional use of EBRT in N1 PC patients are however not conclusive regarding to the extent of radiation field. Even after an EPLND, there might be a role for pelvic EBRT in irradicating microscopic disease. However pelvic irradiation irrevocably results in increased toxicity. Moreover, in node negative (N0) PC patients the addition of pelvic EBRT has not resulted in improved outcome in randomised trials. However in the setting of Tumor Node Metastasis pathological stage (p)N1, proven on pathological examination, PC patients this has never been evaluated so far. This trial aims to answer the question whether or not pelvic EBRT is beneficial in pathological N1 PC patients. It is also important to realise that not all pathological N1 PC patients have similar outcome. There is a significant impact of number of positive lymph nodes on outcome, with two positive nodes being suggested as a significant cut-off value in predicting survival in pathological N1 PC patients. By stratifying the patients according to the number of lymph nodes involved this study will add to the proper selection of those patients who will benefit most of pelvic EBRT and avoid toxicity in patients who have no benefit of pelvic EBRT. Additionally, small RNAs constitute potentially valuable markers for the diagnosis, prognosis, and therapeutic choices in PC patients. Blood samples will be collected to examine the potential role of miRNAs as a biomarker and to develop a prognostic signature for clinical relapse-free survival. The results of this trial will serve as a base for developping new trials in order to optimise the treatment of patients with pathological N1 PC.
Detailed Description
In an era with increasing evidence in favour of an aggressive local treatment, where an extended pelvic lymph node dissection (EPLND) is more frequently performed and with data supporting the potential role for external beam radiotherapy (EBRT) in pelvic node positive (N1) prostate cancer (PC), the treatment of N1 PC patients needs to be revised. Seen the lack of clear guidelines regarding the extent of radiation field in N1 prostate cancer patients, there is an urgent need for studies evaluating the place of pelvic EBRT. The aim of this trial is thus to evaluate if pelvic irradiation has an impact on clinical relapse free survival in pathological N1 PC. The hypothesis is that performing a pelvic EBRT after EPLND in pathological N1 PC patients results in a significant improved clinical relapse free survival with 15% when compared to prostate only EBRT. This will be evaluated in a multicentre Phase III stratified randomised trial randomising patients with PC and 1-4 positive lymph nodes on EPLND between prostate(bed) only radiotherapy + 2 years of ADT or pelvic radiotherapy + 2 years of androgen deprivation. A total of 330 patients will be enrolled in this trial. Stratification is based on the number of positive lymph nodes since patients with increased number of positive lymph nodes exhibit a poorer prognosis.

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
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prostate(bed) only
Arm Type
Experimental
Arm Description
external beam radiotherapy limited to the prostate(bed)
Arm Title
Prostate(bed) and pelvis
Arm Type
Active Comparator
Arm Description
external beam radiotherapy to the prostate(bed) and pelvic lymph node regions
Intervention Type
Radiation
Intervention Name(s)
radiotherapy
Intervention Description
high dose external beam radiotherapy limited to the prostate(bed)
Primary Outcome Measure Information:
Title
Assessment of number of participants without clinical relapse
Description
presence of loco(regional) release or distant metastases
Time Frame
8 years
Secondary Outcome Measure Information:
Title
Assessment of number of participants experiencing Radiation Therapy Oncology Group toxicity
Description
acute
Time Frame
5 years
Title
Assessment of number of participants experiencing Radiation Therapy Oncology Group toxicity
Description
late
Time Frame
10 years
Title
Assessment of number of participants with biochemical control
Description
absence of prostate specific antigen relapse
Time Frame
8 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histological proven carcinoma of the prostate Positive lymph nodes found on extended pelvic dissection (EPLND) defined as: Removal of the lymphatic tissue in the obturator fossa + along the external iliac vessels + additional complete resection of the lymph nodes (lnn) along, medially and laterally to, the hypogastric vessels If technically feasible: removal of lnn along the common iliac vessels Removal of ≥10 lnn Treatment of the primary tumor by either radical prostatectomy or EBRT Willing to receive androgen deprivation therapy World health organization 0-2 Written informed consent Exclusion Criteria:• >4 positive lnn found on EPLND Prior pelvic irradiation Other primary tumor (except for non-melanoma skin tumors) diagnosed <5 years before enrollment Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valérie Fonteyne, Prof
Organizational Affiliation
University Hospital, Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ghent University Hospital
City
Ghent
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Evaluating the Impact of Prostate Only Versus Pelvic Radiation for N+ Prostate Cancer.

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