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临床试验/NCT01075802
NCT01075802已完成不适用

A Multi-Centre Study of Tamoxifen Dose Escalation Study in Breast Cancer Patients With CYP2D6 Polymorphisms

Western Sydney Local Health District2 个研究点 分布在 1 个国家目标入组 121 人开始时间: 2010年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
121
试验地点
2
主要终点
Effects of genotype of CYP2D on plasma and serum concentration of tamoxifen and its metabolites, with consequent recommendation for dosage adjustment

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ECOG performance status ≤ 1
  • Life expectancy ≥ 6 months
  • Histologically or cytologically confirmed early, locally advanced or metastatic breast cancer
  • Oestrogen receptor positive
  • About to start tamoxifen treatment or already on tamoxifen 20mg daily
  • Adequate hepatic and renal function

排除标准

  • Concurrent chemotherapy or radiotherapy
  • Treatment with medications that may alter cytochrome P450 (CYP450)3A4/5 and CYP2D6 activities
  • History of thrombosis
  • History of non-compliance with previous or current treatment;
  • Medical or psychiatric conditions that compromise the patient's ability to give informed consent

研究组 & 干预措施

Tamoxifen

Experimental

Dose escalation of tamoxifen in patients with low endoxifen levels

干预措施: Tamoxifen (Drug)

结局指标

主要结局

Effects of genotype of CYP2D on plasma and serum concentration of tamoxifen and its metabolites, with consequent recommendation for dosage adjustment

时间窗: dose escalation over 40 weeks

Correlate tamoxifen and its metabolites concentration with tamoxifen side effects

时间窗: 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

时间窗: Dose escalation over 40 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Howard Gurney

A/Prof Howard Gurney

Western Sydney Local Health District

研究点 (2)

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