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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| intervention/treatment | Experimental | Total lymphoid irradiation 4 Gy (days -7, -6) in combination with:
|
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| conditioning with TLI | Other | Total lymphoid irradiation 4 Gy (days -7, -6) in combination with:
|
| Measure | Description | Time Frame |
|---|---|---|
| Overall survival | 2 years post HSCT | |
| event free survival | events - death, graft failure, secondary malignancy, relapse of malignancy | 2 years post HSCT |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative incidence of transplant related mortality | 2 years post HSCT | |
| Cumulative incidence of graft failure | non-engraftment, secondary graft rejection, severe non-reversible bone marrow failure |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dmitry Balashov, MD, PhD | Contact | 84956647078 | Dmitriy.Balashov@fccho-moscow.ru | |
| Alexandra Laberko, MD | Contact | 84956647078 | 6223 |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| HSCT department | Moscow | 117198 | Russia |
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| ID | Term |
|---|---|
| C537592 | Neutropenia, Severe Congenital, Autosomal Recessive 3 |
| D000077428 | GATA2 Deficiency |
| ID | Term |
|---|---|
| D009190 | Myelodysplastic Syndromes |
| D001855 | Bone Marrow Diseases |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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|
| 2 years post HSCT |
| Cumulative incidence of graft versus host disease | 2 years post HSCT |
| number of patients with donor chimerism | 2 years post HSCT |
| Incidence of secondary malignancies | number of patients | 2 years post HSCT |
| Cumulative incidence of engraftment | 100 days post HSCT |
| Incidence of early severe organ toxicity | number of patients | 100 days post HSCT |
| cumulative incidence of infectious complications | infectious complication - CMV, EVB, ADV reactivation | 1 year after HSCT |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |