For patients receiving Faslodex 500 mg, to compare the effectiveness in terms of Time to Progression (TTP) as a function of the line of treatment (i.e. 1st vs. 2nd vs. 3rd line). For all patients, to collect and explore real-life data on the epidemiology and management of Pseudomyxoma Peritonea (PMP) patients with HR+ advanced breast cancer (ABC) treated with Faslodex 500 mg or exemestane.
Study Type
OBSERVATIONAL
Enrollment
570
Evaluation of the effectiveness of Faslodex 500 mg in terms of time to progression (TTP) of disease.
Time frame: Period from inclusion up to 9 months (average time period )
Disease management data
The analysis will be adjusted for the main prognostic factors, such as visceral metastases, age, receptor status etc
Time frame: Period from inclusion up to 9 months (average time period )
Real-life data on patient outcomes by line of treatment (i.e. 1st vs. 2nd vs. 3rd line).
Including overall survival (OS), progression-free survival (PFS),time to progression (TTP), response rate (RR) and clinical benefit rate (CBR)
Time frame: Every 3 months
Real-life pharmacoeconomic data and use of health care resources.
According to lines of treatment and other patient related factors (such as age, co-morbidities etc.), including primary care visits, hospital stays and other resource
Time frame: Every 3 months
Health-related quality of life (HRQoL) in patients undergoing treatment with Faslodex 500 mg or exemestane.
Health-related quality of life will be assessed with a patient-based instrument (eg, EQ5D).
Time frame: Every 3 months
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Research Site
Aachen, Germany
Research Site
Ahaus, Germany
Research Site
Amberg, Germany
Research Site
Aschaffenburg, Germany
Research Site
Aschersleben, Germany
Research Site
Bad Nauheim, Germany
Research Site
Bad Segeberg, Germany
Research Site
Bamberg, Germany
Research Site
Bergisch Gladbach, Germany
Research Site
Berlin, Germany
...and 82 more locations