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Effects of EPA on Prostate Cancer Cells Proliferation and Quality of Life (RCT-EPA)

Primary Purpose

Prostate Cancer

Status
Active
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
EPA
Placebo
Sponsored by
CHU de Quebec-Universite Laval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostatectomy, Omega-3 fatty acids, Quality of life, inflammation, cellular proliferation

Eligibility Criteria

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

Inclusion Criteria:

  • Prostate cancer (Gleason score >= 7)
  • Patient has chosen to undergo radical prostatectomy
  • Patient agrees to stop taking any omega-3 supplements at least 3 months before the start of the study
  • Patient has provided informed consent

Exclusion Criteria:

  • Allergy to fish and sunflower
  • Suffering from a bipolar disorder

Sites / Locations

  • Centre de Recherche Clinique et Evaluative en Oncologie - Hotel Dieu de Quebec

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Purified EPA group

Placebo group

Arm Description

3g per day of purified EPA, capsules, to be taken once a day, for 14 months.

3 g per day of high-oleic sunflower oil capsules, to be taken once a day, for 14 months.

Outcomes

Primary Outcome Measures

Change in Prostate Cancer Proliferative Index
At 6 weeks post study entry, the prostate of the patient will be removed by prostatectomy. The tissue will be preserved in paraffin blocks. The tumour will be identified and the level of Ki-67 in the tumour will be quantified.

Secondary Outcome Measures

Change in Inflammatory mediators levels- Systemic
The changes in levels of systemic inflammatory mediators, relative to their baseline levels, at the time of radical prostatectomy and at one year post-radical prostatectomy, will be measured. The levels of mediators will be expressed in pg/mL and quantified using validated techniques.
Modulation of Inflammatory mediators levels - Prostatic
The differences in the levels of expression of inflammatory mediators between both treatment groups will be measured in the peripheral zone of the prostate before surgical prostate dissection/ischemia. The levels of mediators will be expressed in pg/mL and quantified using validated techniques. Further validation could be performed using immunohistochemistry techniques.
Modulation of the Quality of life of patients
Validated questionnaires will be used to measure the modulation of the treatment on Quality of Life of the patients, which will include questions on mood, anxiety levels, sleep and cognition.
Modulation of the psychosocial functioning of patients
Validated questionnaires will be used to measure the modulation of the treatment on psychosocial functioning of the patients, which will include questions on mood, anxiety levels, sleep and cognition.
Impact of inflammation on Quality of life
The impact of changes in inflammatory mediators levels induced by EPA supplementation on quality of life scores will be measured. To do so, we will use appropriate and powerful statistical tests.
Impact of inflammation on psychosocial functioning
The impact of changes in inflammatory mediators levels induced by EPA supplementation and changes in psychosocial functioning scores will be measured. To do so, we will use appropriate and powerful statistical tests.

Full Information

First Posted
December 17, 2014
Last Updated
June 6, 2023
Sponsor
CHU de Quebec-Universite Laval
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1. Study Identification

Unique Protocol Identification Number
NCT02333435
Brief Title
Effects of EPA on Prostate Cancer Cells Proliferation and Quality of Life
Acronym
RCT-EPA
Official Title
Étude randomisée, contrôlée, de Phase II, Effets d'un Supplement d'oméga-3 (EPA) Sur l'Inflammation, la prolifération Cellulaire et la qualité de Vie Chez Des Patients Avec Cancer de la Prostate traités Par Prostatectomie Radicale
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2015 (Actual)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CHU de Quebec-Universite Laval

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prostate cancer, the most frequently diagnosed cancer among occidental men, is associated with a major individual and societal burden. Although still controversial, the literature suggests that a high consumption of omega-3 fatty acids (ω3) has protective effects against prostate cancer. One of the proposed mechanisms of action of ω3 lies in their anti-inflammatory properties. In addition, there are some observational evidences suggesting an association of ω3 intake with a lower rate of depression in cancer patients. However, no clinical study has tested the efficacy of ω3 supplementation on psychological and quality of life outcomes in that population. Several evidences point to a possible involvement of inflammation in psychological issues. Reducing the systemic inflammatory state may have beneficial impact on the quality of life of these patients. Preliminary work from this team of investigators, in a cohort of patients managed with active surveillance for their low-grade prostate cancer, show a strong inverse association between the risk of prostate cancer progression (to high-grade) and the level of prostatic eicosapentanoic acid (EPA- a type of ω3). HYPOTHESIS: EPA-rich monoglycerides fish oil (MAG-EPA) has global positive effects on prostate cancer cell proliferation, inflammation and on the patient's psychosocial functioning and quality of life. The investigators propose a double blind, randomized controlled clinical trial. 130 consecutive patients suffering from high-risk prostate cancer who choose to be treated by radical prostatectomy will be eligible to this study. The presence of high-grade cancer will be mandatory. The intervention, a daily supplementation with 3g supplement of fish oil monoglycerides rich in EPA, vs. placebo capsules containing high oleic sunflower oil, will start six weeks before the prostatectomy and will continue for one year after surgery. The potential confounding variables will be measured before the start of the intervention: age, anthropometric parameters, stage and clinical and pathological tumor grade (Gleason score), pre-operative level of prostate specific antigen and diet. This project proposes a simple intervention by dietary supplementation that could eventually help to reduce the incidence and/or progression of prostate cancer, and the consequences of its treatment, and thus could contribute to diminish the heavy individual and societal burden of prostate cancer. The clinical data generated by this trial will serve as solid basis for a large-scale phase III clinical trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostatectomy, Omega-3 fatty acids, Quality of life, inflammation, cellular proliferation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Purified EPA group
Arm Type
Experimental
Arm Description
3g per day of purified EPA, capsules, to be taken once a day, for 14 months.
Arm Title
Placebo group
Arm Type
Experimental
Arm Description
3 g per day of high-oleic sunflower oil capsules, to be taken once a day, for 14 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
EPA
Intervention Description
3g/day of purified EPA , capsules, taken once daily, for 14 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Other Intervention Name(s)
High oleic sunflower oil
Intervention Description
3g/day of placebo (high oleic sunflower oil) , capsules, taken once daily, for 14 months
Primary Outcome Measure Information:
Title
Change in Prostate Cancer Proliferative Index
Description
At 6 weeks post study entry, the prostate of the patient will be removed by prostatectomy. The tissue will be preserved in paraffin blocks. The tumour will be identified and the level of Ki-67 in the tumour will be quantified.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Change in Inflammatory mediators levels- Systemic
Description
The changes in levels of systemic inflammatory mediators, relative to their baseline levels, at the time of radical prostatectomy and at one year post-radical prostatectomy, will be measured. The levels of mediators will be expressed in pg/mL and quantified using validated techniques.
Time Frame
6 weeks, 1 year
Title
Modulation of Inflammatory mediators levels - Prostatic
Description
The differences in the levels of expression of inflammatory mediators between both treatment groups will be measured in the peripheral zone of the prostate before surgical prostate dissection/ischemia. The levels of mediators will be expressed in pg/mL and quantified using validated techniques. Further validation could be performed using immunohistochemistry techniques.
Time Frame
6 weeks, 1 year
Title
Modulation of the Quality of life of patients
Description
Validated questionnaires will be used to measure the modulation of the treatment on Quality of Life of the patients, which will include questions on mood, anxiety levels, sleep and cognition.
Time Frame
6 weeks, 3, 6, 9 and 12 months post radical prostatectomy
Title
Modulation of the psychosocial functioning of patients
Description
Validated questionnaires will be used to measure the modulation of the treatment on psychosocial functioning of the patients, which will include questions on mood, anxiety levels, sleep and cognition.
Time Frame
6 weeks, 3, 6, 9 and 12 months post radical prostatectomy
Title
Impact of inflammation on Quality of life
Description
The impact of changes in inflammatory mediators levels induced by EPA supplementation on quality of life scores will be measured. To do so, we will use appropriate and powerful statistical tests.
Time Frame
6 weeks, 3, 6, 9 and 12 months post radical prostatectomy
Title
Impact of inflammation on psychosocial functioning
Description
The impact of changes in inflammatory mediators levels induced by EPA supplementation and changes in psychosocial functioning scores will be measured. To do so, we will use appropriate and powerful statistical tests.
Time Frame
6 weeks, 3, 6, 9 and 12 months post radical prostatectomy
Other Pre-specified Outcome Measures:
Title
Fatty acid profiles in red blood cell membranes, change relative to baseline
Description
The difference of fatty acid levels between both groups, relative to baseline, will be quantified using gas chromatography coupled with mass spectrometry and expressed as relative percentages of total fatty acids.
Time Frame
6 weeks, 3, 6, 9, 12 months post radical prostatectomy
Title
Fatty acid profiles in prostate tissue
Description
The difference of fatty acid levels between both groups at prostatectomy will be quantified using gas chromatography coupled with mass spectrometry and expressed as relative percentages of total fatty acids, and in absolute level (mg per gram of tissue).
Time Frame
6 weeks
Title
Impact of EPA supplementation on radical prostatectomy complications
Description
The difference in perioperative bleeding, laboratory tests (hemoglobin, hematocrit and platelets) and surgical complications between both group will be examined at surgery.
Time Frame
6 weeks
Title
Impact of EPA supplementation on cancer aggressiveness
Description
Pathological reclassification of cancer grade (ISUP grading system) and stage between the prostate diagnostic biopsy and the prostatectomy specimen will be compared between both groups.
Time Frame
6 weeks
Title
Change on PSA level (ng/mL), relative to baseline
Description
PSA change relative to baseline will be measured for both groups.
Time Frame
6 weeks, 3, 6, 9 and 12 months post radical prostatectomy
Title
Impact of EPA supplementation on biochemical recurrence
Description
The biochemical recurrence, defined as a PSA level ≥ 0.2 ng/mL after reaching a non-detectable level at three months post-surgery, will be evaluated for both groups.
Time Frame
5 years post radical prostatectomy

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prostate cancer (Gleason score >= 7) Patient has chosen to undergo radical prostatectomy Patient agrees to stop taking any omega-3 supplements at least 3 months before the start of the study Patient has provided informed consent Exclusion Criteria: Allergy to fish and sunflower Suffering from a bipolar disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vincent Fradet, MD, PhD
Organizational Affiliation
Laval University and Hotel Dieu-de-Quebec
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre de Recherche Clinique et Evaluative en Oncologie - Hotel Dieu de Quebec
City
Quebec
ZIP/Postal Code
G1R 3S1
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29321047
Citation
Guertin MH, Robitaille K, Pelletier JF, Duchesne T, Julien P, Savard J, Bairati I, Fradet V. Effects of concentrated long-chain omega-3 polyunsaturated fatty acid supplementation before radical prostatectomy on prostate cancer proliferation, inflammation, and quality of life: study protocol for a phase IIb, randomized, double-blind, placebo-controlled trial. BMC Cancer. 2018 Jan 10;18(1):64. doi: 10.1186/s12885-017-3979-9.
Results Reference
derived

Learn more about this trial

Effects of EPA on Prostate Cancer Cells Proliferation and Quality of Life

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