The aim of the current study is to evaluate the safety and efficacy of low dose treosulfan based conditioning regimen in HSCT in Nijmegen breakage syndrome
Nijmegen breakage syndrome (NBS) is a DNA repair disorder. The only curative option for combine immunodeficiency in NBS is allogeneic hematopoietic stem cell transplantation (HSCT). Standard myeloablative conditioning regimens in DNA repair disorders lead to increased morbidity and mortality after HSCT. Low doses of alkylators are used to reduce toxicity rates, which, however, increase the risks of mixed chimerism and graft failure. The data of treosulfan usage in NBS are sparse. To evaluate the safety and efficacy of low dose treosulfan based conditioning regimen in NBS, treosulfan 21g/m2 in combination with fludarabine 150mg/mg, cyclophosphamide 40mg/kg, thymoglobulin (Genzyme) 5mg/kg and rituximab 100mg/m2 will be used from day -6 to -1 day, followed by stem cell infusion. The primary endpoint is event-free survival, where graft failure, death, and malignancies are considered as events.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Treosulfan 21mg/m2 (days -6, -5, -4)
HSCT department
Moscow, Russia
RECRUITINGEvent-free survival
Events: graft failure, death, malignancies
Time frame: 3 years after HSCT
Overall survival
Time frame: 3 years after HSCT
Cumulative incidence of engraftment
Time frame: 100 days
Cumulative incidence of graft failure
Time frame: 3 years
Cumulative incidence of viral infections
Time frame: 1 year
Cumulative incidence of acute graft versus host disease
Time frame: 1 year
Cumulative incidence of chronic graft versus host disease
Time frame: 3 years
Incidence of early organ toxicity
Time frame: 100 days
Cumulative incidence of transplant related mortality
Time frame: 3 years
Incidence of long-term toxicity
malignancies, non-malignant complications
Time frame: 3 years
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