Palbociclib, the first oral CDK4/6 inhibitor, is an approved medicine indicated for the treatment of a kind of advanced/metastatic breast cancer (MBC), called hormone receptors positive (HR+)/ Human epidermal growth factor receptor 2 negative (HER2-) disease. Palbociclib is given orally in combination with hormonal therapies. The purpose of this study is to better understand how Palbociclib combination is used in real-life conditions and its clinical impact compared with hormonal therapy. The study will also evaluate how long patients take the different CDK 4/6 inhibitor drugs and whether using those drugs impacts the use of chemotherapy later. Male and female patients aged 18 years old or more presenting the following conditions will be selected for the study: * HR+/HER2- MBC * First treatment with Palbociclib, hormonal therapy, or other CDK4/6 inhibitors after MBC diagnosis The study will use data without personal identity, which were obtained from medical records in routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
1
CDK4/6 inhibitor
Aromatase inhibitor
CDK4/6 inhibitor
CDK4/6 inhibitor
Pfizer New York
New York, New York, United States
Overall Survival (OS)
Time frame: From start of index line of therapy to death, February 2015 - December 2022 or data cutoff
Real Progression Free Survival (rwPFS)
Time frame: From start of index line of therapy to death or disease progression, February 2015 - December 2022 or data cutoff
Progression Free Survival 2
Time frame: from start of index treatment to disease progression on the 2nd line of therapy or death, February 2015 - December 2022 or data cutoff
Real-World Tumor Response (rwTR)
Time frame: From start of index treatment to tumor response, February 2015 - December 2022 or data cutoff
Duration of treatment
Time frame: from index treatment initiation to end of the treatment, February 2015 - December 2022 or data cutoff
Time to chemotherapy
Time frame: from index treatment initiation to subsequent chemotherapy, February 2015 - December 2022 or data cutoff
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