The purpose of this non-interventional study is to collect data on the efficiency and safety of pomalidomide in combination with dexamethasone in the routine application
Study Type
OBSERVATIONAL
Enrollment
151
iOMEDICO AG
Freiburg im Breisgau, Baden-Wurttemberg, Germany
Progression free survival (PFS)
Time frame: 6 years
Overall Response Rate (ORR)
Time frame: 6 years
Time to Treatment Discontinuation (TTD)
Time frame: 6 years
Time to next treatment (TNT)
Time frame: 6 years
adverse reaction profile
Time frame: 3 years
secondary malignancies
long term safety is focused on secondary malignancies
Time frame: 6 years
overall Survival (OS)
Time frame: 6 years
relative dose intensity of pomalidomide and dexamethasone
Time frame: 3 years
assess changes in myeloma-related quality of life
Time frame: 3 years
explore additional supportive therapies
To explore additional supportive therapies used on this patient population (e.g. G-CSF, antibiotics, DVT prophylaxis)
Time frame: 3 years
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