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CompletedNCT01075802TADEUpdated May 6, 2013

Study of Tamoxifen Dose Escalation in Breast Cancer Patients With CYP2D6 Polymorphisms

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

Phase
Not applicable
Study type
Interventional
Enrollment
121
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Breast Cancer
  • CYP2D6 Polymorphism

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Keywords

  • Breast cancer
  • Tamoxifen
  • Endoxifen
  • polymorphism of CYP2D6
03

In context

Breast Neoplasms

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.

Browse Breast Neoplasms studies →

Lead sponsor

Western Sydney Local Health District is the lead sponsor of 35 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
121 participants (actual)

Study arms

  • Experimental
    Tamoxifen

    Dose escalation of tamoxifen in patients with low endoxifen levels

    Drug: Tamoxifen

Interventions

  • DrugTamoxifen

    Dose escalation

06

What researchers measure

Primary outcomes

  1. 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

  2. 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

  3. Correlate tamoxifen and its metabolites concentration with tamoxifen side effects

    Time frame: dose escalation over 40 weeks

07

Study locations

2 sites
  • St George Hospital
    Sydney, New South Wales, Australia
  • Westmead Cancer Care Centre
    Westmead, New South Wales 2145, Australia
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01075802
Lead sponsor
Western Sydney Local Health District
Collaborators
St George Hospital, Australia
Responsible party
Howard Gurney (A/Prof Howard Gurney, Western Sydney Local Health District) — Principal investigator
First posted
Feb 25, 2010
Start date
Mar 2010
Primary completion
Oct 2012
Completion
Dec 2012
Last update
May 6, 2013

Study contacts

Howard Gurney, MBBS,FRACP
principal investigator · South West Sydney Local Health District

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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