This is a non-interventional, multi-country, multi-centre, multicohort, primary data collection study, designed to assess patients' reported satisfaction with Atezolizumab Subcutenous (SC) treatment and Health-related Quality of Life (HRQoL), as well as the effectiveness and safety of Atezolizumab SC in participants treated for selected approved indications in routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
700
Atezolizumab will be administered at the discretion of the treating physician and independently of participation in this study.
Landesklinikum Krems
Krems, Austria
RECRUITINGOrdensklinikum Linz Elisabethinen
Linz, Austria
RECRUITINGKrankenhaus Nord - Klinik Floridsdorf
Vienna, Austria
RECRUITINGKlinikum Wels-Grieskirchen
Wels, Austria
Therapy Administration Satisfaction Questionnaire Subcutaneous (TASQ-SC) Score
Time frame: At Cycle 2 and Cycle 3 (each cycle duration/length is 3 weeks)
Overall Survival (OS)
Time frame: Index date up to approximately 3.5 years
OS at 2 Years
Time frame: After Index date up to 2 years
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQ-C30) Score
Time frame: Baseline or Index date
Percentage of Participants With Adverse Events
Time frame: Up to approximately 3.5 years
Reference Study ID Number: MO45893 https://forpatients.roche.com/
CONTACT
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AZ Sint Lucas (Sint Lucas)
Ghent, Belgium
RECRUITINGCHU HELORA - Hôpital de la Louvière - Site Jolimont
Haine-Saint-Paul, Belgium
RECRUITINGCHU UCL Mont-Godinne
Mont-godinne, Belgium
RECRUITINGMultiprofile Hospital for Active Treatment Uni Hospital
Panagyurishte, Bulgaria
RECRUITINGComplex Oncological Center-Ruse EOOD
Rousse, Bulgaria
RECRUITINGTokuda Hospital
Sofia, Bulgaria
RECRUITING...and 76 more locations