The aim of the non-interventional study is to prospectively collect and analyze data on the geriatric assessment of patients undergoing systemic 1st line therapy with trabectedin with focus on patients who have been assessed by the treating physician as being unsuited to receive standard chemotherapy with anthracyclines and / or ifosfamide. Trabectedin will be used according to the local SmPC. Modification of the treatment schedule should follow the standard medical practice at the discretion of the treating physician and is not part of this Observational Plan.
Study Type
OBSERVATIONAL
Enrollment
72
This is a NIS. No intervention.
Klinikum Klagenfurt am Wörthersee
Klagenfurt, Austria
Medizinische Universität Wien
Vienna, Austria
HELIOS Klinikum Bad Saarow
Bad Saarow, Germany
HELIOS Klinikum Berlin Buch
Berlin, Germany
Klinikum Spandau
Berlin, Germany
Universitätsklinikum Carl Gustav Carus der TU Dresden
Dresden, Germany
Universitätsklinikum Heidelberg
Heidelberg, Germany
University of Heidelberg Mannheim University Medical Center Interdisciplinary Tumor Center, Sarcoma Unit
Mannheim, Germany
Klinikum Nürnberg Nord
Nuremberg, Germany
Universitätsklinikum Ulm
Ulm, Germany
...and 2 more locations
Overall survival
Overall survival for each patient will be followed until the end of the study that is defined by 12 months after inclusion of the last patient.
Time frame: 12 month after LPFV
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