Evaluation and Predictive Value of Genetic Polymorphisms in the Management of Hormonal Treatment of Prostate Cancer

NCT ID: NCT02440802

Last Updated: 2016-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-04-30

Study Completion Date

2017-09-30

Brief Summary

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Androgen deprivation therapy (ADT) by surgical castration or administration of LHRH agonists or antagonists is the gold-standard systemic treatment of Prostate Cancer. The efficacy, severity and frequency of side effects of ADT vary from a patient to another. The exact cause of this variability is not known, however certain genetic polymorphisms affecting enzymes implicated in the synthesis and metabolism of sex-steroids seem to be involved in these processes.

To perform a longitudinal study to evaluate the prevalence of various genetic polymorphisms affecting genes in the sex-steroid synthesis and metabolism pathway (CYP1A1, CYP1B1, CYP19A1, 17HSD, HSD3B1, AR, ESR1, ESRRG, IL6, TNF-alpha) in men with Prostate Cancer receiving ADT and the possible association between polymorphisms and frequency and severity of side-effects of ADT.

Detailed Description

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Prostate cancer patients for which reimbursed ADT with a gonadoliberin antagonist is indicated, for a period of at least 6 months will lbe enrolled. At 0, 3 months and 6 months of ADT, Aging Males' Symptoms (AMS), EQ-5D (EuroQoL), and hot flashes intensity and frequency (Moyad scale) will be collected, as well as routine assessments: vital signs (blood pressure, heart rate), weight, waist perimeter, fat percentage, Body Mass Index (BMI) and routine laboratory assessments. Determine genotypes of polymorphisms of interest by pyrosequencing. Determine the prevalence of the polymorphisms of interest in the studied population. Perform initial assessment of the association between genetic polymorphisms and questionnaire results.

Conditions

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Prostate Cancer

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Gonadoliberin antagonist treatment

Single arm study, all patients are treated the same way. Saliva sample collection for genetic analyses.

Saliva sample collection for genetic analyses

Intervention Type GENETIC

Patients with Prostate cancer receiving androgen deprivation treatment with a GnRH antagonist will be followed-up for 6 months for quality of life. At Baseline, 3 months and 6 months of treatment QoL data will be collected, as well as body parameters. At Baseline, once, a saliva sample will be collected for genetic analyses.

Interventions

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Saliva sample collection for genetic analyses

Patients with Prostate cancer receiving androgen deprivation treatment with a GnRH antagonist will be followed-up for 6 months for quality of life. At Baseline, 3 months and 6 months of treatment QoL data will be collected, as well as body parameters. At Baseline, once, a saliva sample will be collected for genetic analyses.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* Prostate cancer patients for which reimbursed ADT with a gonadoliberin antagonist is indicated, for a period of at least 6 months.

Exclusion Criteria

* Prostate cancer patients who are already receiving ADT with a gonadoliberin antagonist.
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Ferring Pharmaceuticals

INDUSTRY

Sponsor Role collaborator

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bertrand TOMBAL, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Cliniques Universitaires Saint Luc, Brussels

Locations

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ASZ Aalst

Aalst, , Belgium

Site Status RECRUITING

OLV Aalst

Aalst, , Belgium

Site Status RECRUITING

ZNA Middelheim

Antwerp, , Belgium

Site Status RECRUITING

CHu Saint Pierre

Brussels, , Belgium

Site Status RECRUITING

Hopital Erasme

Brussels, , Belgium

Site Status RECRUITING

Cliniques Universitaires Saint Luc

Brussels, , Belgium

Site Status RECRUITING

AZ Sint Blasius

Dendermonde, , Belgium

Site Status RECRUITING

JESSA Ziekenhuis

Hasselt, , Belgium

Site Status RECRUITING

Jan Ypermanziekenhuis

Ieper, , Belgium

Site Status WITHDRAWN

CHU Tivoli

La Louvière, , Belgium

Site Status RECRUITING

CHR Citadelle

Liège, , Belgium

Site Status RECRUITING

AZ Sint Jozef

Malle, , Belgium

Site Status WITHDRAWN

ZNA Jan Palfijn

Merksem, , Belgium

Site Status RECRUITING

CH Mouscron

Mouscron, , Belgium

Site Status RECRUITING

Clinique Saint Luc Bouge

Namur, , Belgium

Site Status RECRUITING

AZ Damiaan

Ostend, , Belgium

Site Status RECRUITING

AZ Delta

Roeselare, , Belgium

Site Status RECRUITING

AZ St Jozef

Turnhout, , Belgium

Site Status RECRUITING

AZ Jan Portaels

Vilvoorde, , Belgium

Site Status RECRUITING

CHU Mont-Godinne

Yvoir, , Belgium

Site Status RECRUITING

Countries

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Belgium

Central Contacts

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Bertrand TOMBAL, MD, PhD

Role: CONTACT

003227641409

Valentina BUTOESCU, PharmD

Role: CONTACT

003227643546

Facility Contacts

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Bernard RAPPE, MD

Role: primary

Peter SCHATTEMAN, MD

Role: primary

Tibaut DEBACKER, MD

Role: primary

Kim Entezari, MD

Role: primary

Thierry ROUMEGUERE, MD

Role: primary

Bertrand TOMBAL, MD, PhD

Role: primary

003227641409

Valentina BUTOESCU, PharmD

Role: backup

003227643546

Dieter OST, MD

Role: primary

Kris VEKEMANS, MD

Role: primary

Thierry WILDSCHUTZ, MD

Role: primary

Hubert NICOLAS, MD

Role: primary

Peter DE JONGE, MD

Role: primary

Philippe FRANCOIS, MD

Role: primary

Luc DE VISSCHER, MD

Role: primary

Pieter MATTELAER, MD

Role: primary

Lieven GOEMAN, MD

Role: primary

Koen Ackaert, MD

Role: primary

Geert Martens, MD

Role: primary

Francis LORGE, MD

Role: primary

References

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Other Identifiers

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B403201317385

Identifier Type: -

Identifier Source: org_study_id

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