Planned study population consists of approximately 240 adult patients with HER2-positive mBC receiving anti-HER2 therapy in 12 oncological centers (in each center it is expected to recruit about 20 patients) in different regions in order to provide representative study sample. Patients will be included consecutively from the least recent diagnosis (within defined time period). Planned retrospective follow-up period for 1 patient is a period starting from the date of mBC diagnosis until end study or until patient's death, whichever occurs first. End of study will be at least 12 months after the latest date of mBC diagnosis to ensure all patients have the opportunity to contribute at least 12 months of data.
Study Type
OBSERVATIONAL
Enrollment
240
'Regional Cancer Centre' Uralsk
Oral, Kazakhstan, Kazakhstan
Medical Centre of the Marat Ospanov West Kazakhstan Medical University, Aktobe
Aktobe, Kazakhstan
'Kazakh Research Institute of Oncology and Radiology (KAZNIOR)'
Almaty, Kazakhstan
Almaty Cancer Centre
Almaty, Kazakhstan
'Multidisciplinary Medical Centre' of the Astana City Administration
Astana, Kazakhstan
National Cancer Research Centre, Astana
Astana, Kazakhstan
'Karaganda General Hospital No. 3' of the Karaganda Region Health Department
Karaganda, Kazakhstan
'General Regional Hospital' of the municipal state institution 'Health Department of the Akimat of North Kazakhstan Region' Petropavlovsk
Petropavl, Kazakhstan
'Centre for Nuclear Medicine and Oncology' Abai Regional Health Authority Semey
Semey, Kazakhstan
'Shymkent City General Hospital with Oncology Centre' under the Shymkent City Health Department
Shymkent, Kazakhstan
...and 2 more locations
(1) To assess median PFS and PFS rate in patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
To describe the clinical and demographic characteristics of patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
(2) To describe the diagnostic algorithms and therapeutic tactics in patients with HER2-positive mBC in routine practice in Kazakhstan
Time frame: up to 2 years
(3) To describe the treatment approach in patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
(4) To assess the efficacy of anticancer treatment in patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
(5) To describe the reasons for anticancer therapy discontinuation in patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
(6) To assess the number of therapy lines of anticancer treatment in patients with HER2-positive mBC receiving anti-HER2 therapy (except for trastuzumab deruxtecan) in routine practice in Kazakhstan
Time frame: up to 2 years
AstraZeneca Clinical Study Information Center
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