The objective of this study is to compare hematological toxicity, costs, health-related quality of Life (HR-QOL) and outcomes observed in real life in the Belgian Non-Hodgkin Lymphoma (NHL) population receiving 90Y-Zevalin, with model-predicted data at reimbursement on the basis of a clinical trial in heavily pre-treated NHL.
Study Type
OBSERVATIONAL
Enrollment
30
Zevalin was administered according to the directives in the approved package leaflet.
Unnamed facility
Many Locations, Belgium
The medical resources consumed due to hematological adverse events that occurred following treatment with 90Y-Zevalin treatment
Time frame: one year after inclusion
the health related quality of life prior to and following treatment (using EQ-5D and FACT-LYM)
Time frame: baseline: before 1st administration, 8 days after baseline, 1, 2 & 3 months after baseline
the clinical outcomes (survival status, response status), TTNT (time to next treatment)
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.