The purpose of this study is to follow safety and quality of life outcomes on patients switching from tamoxifen therapy to aromatase inhibitor therapy.
Group of patients using the same aromatase inhibitor
Study Type
OBSERVATIONAL
Enrollment
344
non-interventional study
Pfizer Investigational Site
Adana, Turkey (Türkiye)
Pfizer Investigational Site
Ankara, Turkey (Türkiye)
Pfizer Investigational Site
To evaluate the quality of life of patients with early stage postmenopausal breast cancer using aromatase inhibitor following 2-3 years of tamoxifen treatment (switch)
Time frame: 2 years
To evaluate patients with early stage postmenopausal breast cancer using aromatase inhibitor following 2-3 years of tamoxifen treatment (switch) in terms of side effects
Time frame: 2 years
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Ankara, Turkey (Türkiye)
Pfizer Investigational Site
Ankara, Turkey (Türkiye)
Pfizer Investigational Site
Bursa, Turkey (Türkiye)
Pfizer Investigational Site
Denizli, Turkey (Türkiye)
Pfizer Investigational Site
Edirne, Turkey (Türkiye)
Pfizer Investigational Site
Erzurum, Turkey (Türkiye)
Pfizer Investigational Site
Gaziantep, Turkey (Türkiye)
Pfizer Investigational Site
Istanbul, Turkey (Türkiye)
...and 6 more locations