Severe congenital neutropenia (SCN) is a group of primary immunodeficiencies caused by distinct gene mutations and characterized by neutrophil maturation impairment, which leads to neutropenia, predisposition to severe bacterial and fungal infections, and myeloid malignancies. Granulocyte-colony stimulation factor is used for pathogenetic therapy, however, no adequate response is seen in some patients. The only curative option for SCN is hematopoietic stem cell transplantation (HSCT). An indication for HSCT in SCN is: no adequate response to G-CSF therapy, or development of malignancies, or found unfavorable mutations of SCN genes, leading to poor response to G-CSF and high risk of malignant transformation. One of the major peculiarities of HSCT in SCN is a high risk of graft failure. That was described in few studies in SCN transplantation and was also observed in our SCN HSCT cohort. We also consider the role of TCRab/CD19 graft depletion, which is routinely used in our center for GVHD prophylaxis in increased risks of graft failure. Another problem often observed in our patients is the relatively high risks of death of infections, developed after graft failure. Due to predominantly early HSCT graft failure development, non-sufficient immuablation is presumed as the main reason for graft failure. Because of the low level of toxicity, associated with TCRab/CD19 depletion usage, this strategy is planned to be used in the current study. To increase an immunoablative potential of conditioning regimen in SCN, total lymphoid irradiation will be studied in combination with myeloablative agents and standardly used serotherapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Total lymphoid irradiation 4 Gy (days -7, -6) in combination with: * Fludarabine 150 mg/m2 (days-6, -5, -4, -3, -2) * Cyclophosphamide 120 mg/kg (days -5, -4, -3) * Thymoglogulin (Genzyme) 5 mg/kg (days -5, -4) * Melphalan 180 mg/m2 (day -2) * Rituximab 100 mg/m2 (day -1) * Hematopoietic stem cell graft infusion after TCRab/CD19 depletion - day 0
HSCT department
Moscow, Russia
Overall survival
Time frame: 2 years post HSCT
event free survival
events - death, graft failure, secondary malignancy, relapse of malignancy
Time frame: 2 years post HSCT
Cumulative incidence of transplant related mortality
Time frame: 2 years post HSCT
Cumulative incidence of graft failure
non-engraftment, secondary graft rejection, severe non-reversible bone marrow failure
Time frame: 2 years post HSCT
Cumulative incidence of graft versus host disease
Time frame: 2 years post HSCT
number of patients with donor chimerism
Time frame: 2 years post HSCT
Incidence of secondary malignancies
number of patients
Time frame: 2 years post HSCT
Cumulative incidence of engraftment
Time frame: 100 days post HSCT
Incidence of early severe organ toxicity
number of patients
Time frame: 100 days post HSCT
cumulative incidence of infectious complications
infectious complication - CMV, EVB, ADV reactivation
Time frame: 1 year after HSCT
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