This is a prospective study of the safety and efficacy of nivolumab for the treatment of relapsed or residual haematological malignancies after allogeneic stem cell transplantation (alloSCT). Eligible patients will receive nivolumab at a dose of 3mg/kg intravenously every 2 weeks. The primary objective is to evaluate the incidence, severity and treatment responsiveness of GVHD following nivolumab treatment post-alloSCT.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
14
Human monoclonal antibody targeting programmed death-1 (PD-1) cell surface receptor
Royal Melbourne Hospital
Parkville, Victoria, Australia
Graft versus host disease
Cumulative incidence of graft versus host disease
Time frame: 8 weeks
Graft versus host disease
Cumulative incidence of graft versus host disease
Time frame: 24 weeks
Graft versus host disease
Cumulative incidence of graft versus host disease
Time frame: 48 weeks
Overall response rate
Complete remission and partial remission
Time frame: 8 weeks
Overall response rate
Complete remission and partial remission
Time frame: 16 weeks
Overall response rate
Complete remission and partial remission
Time frame: 24 weeks
Overall response rate
Complete remission and partial remission
Time frame: 48 weeks
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