An interventional study of Tamoxifen in Breast Cancer and CYP2D6 Polymorphism, sponsored by Western Sydney Local Health District. Completed at 2 sites in Australia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-05-06.
Sponsored by Western Sydney Local Health District · Not applicable, Interventional, and Diagnostic
Tamoxifen is an important drug for the treatment of breast cancer. Used adjuvantly after operation in early breast cancer, tamoxifen reduces annual recurrence rate by half and cancer death by one third. Used preventatively it also reduces the risk of breast cancer by 50% in women at high risk for developing the disease Tamoxifen needs to be activated in the body to an active form called endoxifen, mainly by the enzyme called CYP2D6. Patients have variable capability to activate tamoxifen due to variable function of this enzyme. Studies showed clear correlation of specific genetic variant of CYP2D6 with endoxifen blood levels. It is estimated that up to 25% Caucasian population have reduced or even absent CYP2D6 function. More recently, there were studies that showed the correlation with genetic variant of CYP2D6 and breast cancer relapse in early breast cancer patients treated with tamoxifen. Food and Drug Authority (FDA) in America and recommended checking CYP2D6 genotype in patients receiving tamoxifen treatment, but they did not specify how to interpret the genotype results and what kind actions to take in patient with adverse genotype. The aim of the investigators study is to see if increasing tamoxifen in patients with genetic polymorphism of CYP2D6 will increase endoxifen level to the same range of most patients who have wild type (normal functional)CYP2D6.
12,543 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.
This study's enrollment of 121 is above the median of 72 across 9,302 interventional studies indexed under Breast Neoplasms.
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Exclusion Criteria:
Dose escalation of tamoxifen in patients with low endoxifen levels
Drug: Tamoxifen
Dose escalation
Effects of genotype of CYP2D on plasma and serum concentration of tamoxifen and its metabolites, with consequent recommendation for dosage adjustment
Time frame: dose escalation over 40 weeks
To test whether Tamoxifen dose escalation in patients with genetic polymorphism of CYP2D6 will increase endoxifen blood levels to a target level
Time frame: Dose escalation over 40 weeks
Correlate tamoxifen and its metabolites concentration with tamoxifen side effects
Time frame: dose escalation over 40 weeks
This study is completed, as verified in May 2013. You cannot join it, but the record below documents what was studied.
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Western Sydney Local Health District