Electronic Patient Reported Outcome (ePRO) measures in patients with Soft Tissue Sarcoma (STS) receiving palliative treatment

The PazoQoL prospective, randomized, controlled, multicenter study was designed to continuously assess global health related quality of life (HRQoL) during treatment with pazopanib or physician-preferred chemotherapy over a 9-week period. The questionnaires were completed by the patients at home wit...

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Hauptverfasser: Hofer, Silvia (VerfasserIn) , Hentschel, Leopold (VerfasserIn) , Richter, Stephan (VerfasserIn) , Blum, Veronika (VerfasserIn) , Kramer, Michael (VerfasserIn) , Kasper, Bernd (VerfasserIn) , Riese, Christoph (VerfasserIn) , Schuler, Markus K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 February 2023
In: Cancers
Year: 2023, Jahrgang: 15, Heft: 4, Pages: 1-8
ISSN:2072-6694
DOI:10.3390/cancers15041233
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/cancers15041233
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2072-6694/15/4/1233
Volltext
Verfasserangaben:Silvia Hofer, Leopold Hentschel, Stephan Richter, Veronika Blum, Michael Kramer, Bernd Kasper, Christoph Riese and Markus K. Schuler

MARC

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520 |a The PazoQoL prospective, randomized, controlled, multicenter study was designed to continuously assess global health related quality of life (HRQoL) during treatment with pazopanib or physician-preferred chemotherapy over a 9-week period. The questionnaires were completed by the patients at home with great reliability during this time period. Continuous electronic patient reported outcome (ePRO) enabled early detection of the onset of deterioration and timely initiation of countermeasures. The Cancer Therapy Satisfaction Questionnaire (CTSQ) showed high interindividual variability and decline over a 9-week period, whereas the Time Trade-off (TTO) proved to be an efficient method for assessing individual benefit from cancer therapy. In our cohort, the TTO clearly demonstrated that the prolongation of life and the side effect profile of continued therapy were not as satisfactory as expected by patients when starting a new therapy. Although the study had to be stopped early due to the pandemic, our findings could translate into clinical practice without much effort and outside of a trial. 
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