Physician
Agoston Guyla Szabo
Department of Medicine, Lillebaelt Hospital, Vejle
Projekt styring | ||
Projekt status | Active | |
Data indsamlingsdatoer | ||
Start | 01.06.2020 | |
Slut | 01.06.2026 | |
The aim of this study is to assess the safety and efficacy of Venetoclax in a reduced dosis of 400 mg daily in combination with dexamethasone in patients with relapsed or refractory multiple myeloma who have translocation t(11;14). This is an open label, phase II, multicenter study that will be conducted in Denmark.
Venetoclax-dexamethasone, although currently not an approved regimen in MM, seems to be a safe and effective treatment option in patients with relapsed and refractory MM, especially in patients who are positive for t(11;14). The aim of this phase II trial is to provide results about the safety and efficacy of this regimen specifically in the subgroup of patients with t(11:14). One of the objectives of this study is to assess the humoral immunodeficiency of subjects and to minimize the risk of pneumonia by anti-pneumococcal vaccination and infection prophylaxis.
Adults with relapsed or refractory multiple myeloma with t(11;14)
Primary end-point
• Overall response rate
Secondary end-points
• Progression-free survival
• Clinical benefit rate
• Time to next treatment
• Overall survival
• Time to response
• Duration of response
• Safety and tolerability
• Discontinuation rate
• Quality of life
• Number of serious adverse events due to infections
• Duration of hospital admissions due to infections
Exploratory end-points
• Estimation of humoral immunodeficiency of subjects at baseline by measuring serum anti-pneumococcal polysaccharide IgG, IgA, IgM antibodies
• Assessment of the relation of humoral immunodeficiency to infections
• Assessment of pneumococcal vaccination response and its relation to infections
• Estimation of Bcl-2 overexpression by immunohistochemistry Assessment of the relation of Bcl-2 overexpression to the efficacy of the study treatment
Department of Hematology, Odense University Hospital
Department of Haematology, Zealand Hospital, Roskilde