Patient's Anastrozole Compliance to Therapy Programme
- 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
- Histological/cytological confirmed primary diagnosis of early breast cancer
- Postmenopausal
- Hormone receptor positive
- 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
Group Intervention Description 1 Anastrozole Standard routine care for breast cancer 2 Anastrozole Standard + Intervention arm: standard routine care for breast cancer and additional information material via post
- Primary Outcome Measures
Name Time Method Compliance rate and persistence rate until discontinuation of treatment
- Secondary Outcome Measures
Name Time Method Time of disease free survival date 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 life until treatment discontinuation The percentage number of patients with disease free survival after 12 months Time to treatment discontinuation date of last intake of anastrozole minus date of first prescription of anastrozole + 1