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Patient's Anastrozole Compliance to Therapy Programme

Terminated
Conditions
Breast Cancer
Interventions
Registration Number
NCT00555867
Lead Sponsor
AstraZeneca
Brief Summary

Approximately 60 specialised clinics and 420 office based gynaecologists or oncologists will participate in this in practice evaluation program (NIS). The clinic and approximately 7 office based physicians will collaborate within their breast centre networks to conduct this program. A breast centre network should be able to recruit in this program approximately 80 patients (approximately 40 patients per year). It is planned to enroll approximately 4674 patients in this NIS (2337 patients per arm). The patient population will include postmenopausal women with hormone-receptor positive primary breast cancer scheduled for upfront adjuvant endocrine treatment with anastrozole according to the current standard medical procedures.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
4923
Inclusion Criteria
  • Histological/cytological confirmed primary diagnosis of early breast cancer
  • Postmenopausal
  • Hormone receptor positive
Exclusion Criteria
  • Patients with severe renal function disorders
  • Patients with moderate or severe disorders of hepatic function
  • Concomitant treatment with drugs known to affect sex hormonal status and tamoxifen

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
1AnastrozoleStandard routine care for breast cancer
2AnastrozoleStandard + Intervention arm: standard routine care for breast cancer and additional information material via post
Primary Outcome Measures
NameTimeMethod
Compliance rate and persistence rateuntil discontinuation of treatment
Secondary Outcome Measures
NameTimeMethod
Time of disease free survivaldate of recurrence or progression of the tumor minus date of primary breast cancer surgery + 1
Demographics and other baseline characteristics as well as information regarding concomitant medication, quality of lifeuntil treatment discontinuation
The percentage number of patients with disease free survivalafter 12 months
Time to treatment discontinuationdate of last intake of anastrozole minus date of first prescription of anastrozole + 1
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