The objective of this study is to investigate the effectiveness of Atezolizumab with a primary focus on the overall survival (OS) rate at 2 years and secondary focuses on quality of life (QoL) and the sequence of treatment in mUC patients. Furthermore, this study aims at collecting data on safety of Atezolizumab and on the reason for cisplatin-ineligibility
Study Type
OBSERVATIONAL
Enrollment
22
Atezolizumab is administered via IV 1200 mg every 3 weeks
Overall Survival Rate (OS rate)
Time frame: 2 years
Median Overall Survival (OS)
Time frame: Initiation of study treatment until death or end of study, approximately 4 years
Median Progression Free Survival (PFS)
Time frame: Initiation of study treatment to first measured disease progression, through end of study (approximately 4 years)
Percentage of participants with adverse events
Time frame: Up to approximately 4 years
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Praxis Dr.med. Wolfgang Hölzer
Berlin, Germany
Urologie Schlosscarree
Braunschweig, Germany
Urologische Praxis Dr. Krieger
Chemnitz, Germany
Zeisigwaldkliniken Bethanien
Chemnitz, Germany
St. Georg Klinikum Eisenach GmbH
Eisenach, Germany
St. Franziskus-Hospital; Malteser Krankenhaus; Medizinische Klinik I
Flensburg, Germany
Klinikum Frankfurt Höchst GmbH; Klinik Innere Medizin 3 - Hämatologie, Onkologie, Palliativmedizin
Frankfurt am Main, Germany
Dres.Jochen Wilke und Harald Wagner
Fürth, Germany
Krankenhaus Martha-Maria Halle-Dölau, Klinik für Urologie
Halle, Germany
Urologische Praxis Michael Steinacker
Halle, Germany
...and 22 more locations