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Surgery Combined With Intensity Modulated Radiation Therapy - Image-Guided Radiation Therapy (IMRT-IGRT) in Locally-advanced Prostate Cancers (TARGET)

Primary Purpose

Prostate Cancer, Prostate Adenocarcinoma

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Surgery combined with IMRT-IGRT
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring IMRT-IGRT, radiotherapy toxicity, seminal vesicles

Eligibility Criteria

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

Inclusion Criteria:

  • Age > 18,
  • Prostate adenocarcinoma (histologically proven),
  • Locally-advanced (T3a or Gleason > 7 or PSA ≥ 20 ng/mL),
  • Distal half of seminal vesicles unaffected on MRI,
  • Non metastatic cancer: negative extension assessment (on prostatic and pelvic MRI and bone scintigraphy),
  • Radiotherapy and hormonotherapy indication,
  • Medical insurance affiliation,
  • Written informed consent.

Non-inclusion criteria:

  • Co-morbidity or medical history contraindicating surgery (pelvic lymphadenectomy and seminal vesicle ablation),
  • Contraindication to pelvic irradiation,
  • Hip prosthesis,
  • History of cancer for the last 5 years (except baso-cellular epithelioma),
  • History of pelvic irradiation,
  • Person deprived of freedom or under guardianship,
  • Participation in another biomedical research.

Exclusion Criteria:

  • Surgery showing lymph nodes involvement (pelvic radiation indication)
  • Surgery without ablation of seminal vesicles
  • Surgery with positive margins in seminal vesicles

Sites / Locations

  • Service d'Urologie - Hôpital de Pontchaillou
  • Centre Eugène Marquis - CRLCC

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Surgery combined with IMRT-IGRT

Arm Description

Outcomes

Primary Outcome Measures

Rate of bladder and/or rectal grade ≥2 toxicity (late toxicity)
Rate of bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) observed between 6 months and 3 years after the beginning of the radiotherapy.

Secondary Outcome Measures

Dose received by the rectum and the bladder with and without seminal vesicles irradiation
Assessed using a dose-volume histogram
Quality of life
Assessed with EORTC questionnaires (QLQ-C30, QLQ-PR25)
Erectile troubles
Assessed with erectile troubles questionnaire (IIEF-5)
Onset of biological signs evocating a recidive
Assessed with PSA levels
Onset of clinical signs evocating a recidive
Specific and global survival
Rate of bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) (early toxicity)
Rate of late bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) observed 6 months after the beginning of the radiotherapy.

Full Information

First Posted
June 18, 2010
Last Updated
December 18, 2018
Sponsor
Rennes University Hospital
Collaborators
Center Eugene Marquis
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1. Study Identification

Unique Protocol Identification Number
NCT01148069
Brief Title
Surgery Combined With Intensity Modulated Radiation Therapy - Image-Guided Radiation Therapy (IMRT-IGRT) in Locally-advanced Prostate Cancers
Acronym
TARGET
Official Title
Surgery Combined With IMRT-IGRT in Locally-advanced Prostate Cancers
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
July 30, 2010 (Actual)
Primary Completion Date
July 4, 2018 (Actual)
Study Completion Date
July 4, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital
Collaborators
Center Eugene Marquis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Standard treatment of locally-advanced prostate cancers consists in the association of radiotherapy of prostate and seminal vesicles (SV) and androgen deprivation (AD) for 3 years. This treatment is usually preceded by pelvic lymphadenectomy to assess the possible extension to lymph nodes of prostatic cancer and to avoid irradiating the pelvis in case of no lymph node involvement. However, radiotherapy leads usually to about 30% of grade ≥2 risk of bladder and/or rectal toxicity. This risk particularly depends on the radiation volume. In the aim of lowering the toxicity, the treatment in this study will associate: pelvic lymph node dissection and resection of seminal vesicles, allowing decreasing the radiation target volume to the prostate only (and not to irradiate the SV); a high-precision radiotherapy technique combining Intensity Modulated Radiation Therapy (IMRT) and Image-Guided Radiation Therapy (IGRT).
Detailed Description
This study targets non metastatic prostatic locally-advanced adenocarcinomas which are at high risk of both local progression and metastases. The standard treatment of these tumours associates external beam radiation therapy (EBRT) and 3 years of androgen deprivation (AD) with LH-RH analogue. In the absence of AD and mainly when prostate specific antigen (PSA) is >10 ng/ml, several randomized studies have shown that high doses of EBRT increase biochemical control. Nevertheless, escalating the doses of radiation significantly increases the risk of rectal and/or urinary toxicities. In order to lower the toxicity of irradiation in locally-advanced prostate cancers, and to improve the quality of life of patients, this study aims at decreasing the volume of irradiated healthy tissues. To carry out this objective, we will use a double strategy: Limiting the target volume to prostate only by removing seminal vesicles at the time of lymph node dissection, Using a technique of high-precision radiation combining Intensity Modulated Radiation Therapy (IMRT) and Image-Guided Radiation Therapy (IGRT). Based on the literature, we may assume a toxicity rate of 30% during the three years of hormonotherapy with standard treatment (i.e. without removing seminal vesicles). We make the hypothesis of a 20% absolute reduction of toxicity with our protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Prostate Adenocarcinoma
Keywords
IMRT-IGRT, radiotherapy toxicity, seminal vesicles

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
63 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgery combined with IMRT-IGRT
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Surgery combined with IMRT-IGRT
Intervention Description
Patients will have surgery consisting in extensive pelvic dissection and ablation of seminal vesicles. Surgery will be followed by prolonged hormonotherapy (3 years) associated, after 2 months, with prostatic only irradiation.
Primary Outcome Measure Information:
Title
Rate of bladder and/or rectal grade ≥2 toxicity (late toxicity)
Description
Rate of bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) observed between 6 months and 3 years after the beginning of the radiotherapy.
Time Frame
between 6 months and 3 years
Secondary Outcome Measure Information:
Title
Dose received by the rectum and the bladder with and without seminal vesicles irradiation
Description
Assessed using a dose-volume histogram
Time Frame
Before treatment
Title
Quality of life
Description
Assessed with EORTC questionnaires (QLQ-C30, QLQ-PR25)
Time Frame
3 years
Title
Erectile troubles
Description
Assessed with erectile troubles questionnaire (IIEF-5)
Time Frame
3 years
Title
Onset of biological signs evocating a recidive
Description
Assessed with PSA levels
Time Frame
3 years
Title
Onset of clinical signs evocating a recidive
Time Frame
3 years
Title
Specific and global survival
Time Frame
3 years
Title
Rate of bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) (early toxicity)
Description
Rate of late bladder and/or rectal grade ≥2 toxicity (CTCAE V4.0) observed 6 months after the beginning of the radiotherapy.
Time Frame
6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18, Prostate adenocarcinoma (histologically proven), Locally-advanced (T3a or Gleason > 7 or PSA ≥ 20 ng/mL), Distal half of seminal vesicles unaffected on MRI, Non metastatic cancer: negative extension assessment (on prostatic and pelvic MRI and bone scintigraphy), Radiotherapy and hormonotherapy indication, Medical insurance affiliation, Written informed consent. Non-inclusion criteria: Co-morbidity or medical history contraindicating surgery (pelvic lymphadenectomy and seminal vesicle ablation), Contraindication to pelvic irradiation, Hip prosthesis, History of cancer for the last 5 years (except baso-cellular epithelioma), History of pelvic irradiation, Person deprived of freedom or under guardianship, Participation in another biomedical research. Exclusion Criteria: Surgery showing lymph nodes involvement (pelvic radiation indication) Surgery without ablation of seminal vesicles Surgery with positive margins in seminal vesicles
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Renaud DE CREVOISIER, MD, PhD
Organizational Affiliation
Rennes CRLCC Eugène Marquis
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sebastien VINCENDEAU, MD
Organizational Affiliation
Rennes University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Eric BELLISSANT, MD, PhD
Organizational Affiliation
Rennes University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Service d'Urologie - Hôpital de Pontchaillou
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
Centre Eugène Marquis - CRLCC
City
Rennes
ZIP/Postal Code
35042
Country
France

12. IPD Sharing Statement

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Surgery Combined With Intensity Modulated Radiation Therapy - Image-Guided Radiation Therapy (IMRT-IGRT) in Locally-advanced Prostate Cancers

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