Prevalence of Genetic Polymorphisms in Genes Coding for Tamoxifen Metabolising Enzymes
Conditions
Breast Neoplasms - Female
Conditions: official terms
Breast Neoplasms
Study Type
Interventional
Study Phase
Phase 3
Study Design
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: blood samples/ ultrasound
Type: Biological
Overall Status
Recruiting
Summary
CYPTAM-BRUT 3 is a prospective, multicentric study in Belgium within the CYPTAM study of the Leiden University Medical Center (NTR1509) including postmenopausal women receiving tamoxifen for estrogen-receptor positive breast cancer in the adjuvant setting. The primary endpoint is the difference in uterine changes between women with a normal versus low TAS after 3 months of tamoxifen use. Secondary endpoints are serum metabolite concentrations, serum follicle-stimulating hormone level, serum sex hormone-binding globulin level and menopausal symptoms. These patients are registered in the Leiden protocol with time to breast cancer event as primary endpoint.
Detailed Description
We will study the impact of the 'tamoxifen activity score' - based on functional genetic polymorphisms for tamoxifen metabolism and the use of drugs that interfere with tamoxifen-against tamoxifen related endpoints like uterine changes and subjective menopausal symptoms.

The prevalence of genetic polymorphisms in the CYP2D6 and other genes and differences in usage of drugs interacting with tamoxifen metabolism will be compared between women with and those without endometrial thickening on one hand and between women with and those without hot flashes on the other hand. Tamoxifen use in adjuvant setting.

- "Tamoxifen activity score" (23): The endpoints will be correlated with a predefined 'tamoxifen activity score' which is based on the presence of single nucleotide polymorphisms (SNP) in relevant genes combined with the effect of well known drugs that interfere with the metabolism of tamoxifen. The 'tamoxifen activity score' has been associated with tamoxifen compliance by a group in the US (23). The score will be adapted to the Belgian situation based on the prevalence of these SNPs in a Belgian population of volunteers for blood donation and consecutive breast cancer patients.

- The study setting are postmenopausal women with an early ER- positive breast cancer and not previously treated with an endocrine agent or hormone replacement therapy, with an intact uterus and clearly measurable thin endometrium/uterus. N =250
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 18 Years
Gender: Female
Criteria: Inclusion Criteria:

- Female > 18 years of age

- Written and voluntary informed consent understood signed and dated

- Histologically or cytologically confirmed measurable invasive adenocarcinoma of the breast, amenable to curative therapy.

- Patients must be postmenopausal as defined by criteria in appendix 1.

- Breast cancer should be considered as oestrogen receptor positive by the clinician using immunohistochemistry readings as is standard procedure for local pathologist

- Prior endocrine tamoxifen therapy is not allowed

- Patients are not previously treated with an endocrine agent or hormone replacement therapy needs being stopped for at least 6 months.

- Prior chemotherapy and radiotherapy is allowed

- Adequate renal and liver function Serum creatinine and serum bilirubin ≤ 1.5 X ULN Serum ALT and AST ≤ 2.5 X ULN (or ≤ 5 in case of liver metastases)

- Serum calcium should be ≤ 11,6 mg/dl

- ECOG performance status 0,1,2 (appendix 2)

Exclusion Criteria:

- Male

- Life threatening disease requiring a quick response (eg, extensive hepatic or pulmonary involvement)

- Use of any endocrine treatment or recent/current use of hormone replacement therapy.

- Contra indication for tamoxifen: history of DVT/vaginal bleeding of unknown origin

- Dementia

- History of other malignancy that may interfere with at least 6 months of tamoxifen therapy
Locations
AZ St-Maarten
Duffel, Antwerpen, Belgium
Status: Not yet recruiting
Contact: chantal Blomme - chantalblomme@hotmail.com
AZ St-Nikolaas
St-Niklaas, Antwerpen, Belgium
Status: Recruiting
Contact: Goele Wallays - goele.wallays@aznikolaas.be
Ziekenhuizen Oost-Limburg Camus St-Jan
Genk, Limburg, Belgium
Status: Not yet recruiting
Contact: Patricia Jarkowski - patricia.jarkowski@zol.be
AZ St-Blasius
Dendermonde, Ookst-Vlaanderen, Belgium
Status: Not yet recruiting
Maria-Middelares
Gent, Oost-Vlaanderen, Belgium
Status: Not yet recruiting
UZ
Gent, Oost-Vlaanderen, Belgium
Status: Not yet recruiting
Contact: Marleen De Block - Marleen.deblock@ugent.be
UZ
Leuven, Vlaams-Brabant, Belgium
Status: Recruiting
Contact: Chantal Blomme - chantalblomme@hotmail.com
Heilig-Hart Ziekenhuis
Roeselare, West-Vlaanderen, Belgium
Status: Not yet recruiting
Institut Bordet
Brussel, Belgium
Status: Not yet recruiting
Contact: Melanie Demol - melanie.demol@bordet.be
UCL
Brussel, Belgium
Status: Not yet recruiting
Contact: Nathalie Blondeel - nathalie.blondeel@clin.ucl.ac.be
UZ
Brussel, Belgium
Status: Not yet recruiting
Contact: Alex dewaele - alex.dewaele@uzbrussel.be
Start Date
June 2009
Completion Date
December 2010
Sponsors
Vlaamse Vereniging voor Obstetrie en Gynaecologie
Source
Vlaamse Vereniging voor Obstetrie en Gynaecologie
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page