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Targeted busulfan and fludarabine-based conditioning for bone marrow transplantation in chronic granulomatous disease

Chronic granulomatous disease (CGD) is a primary immunodeficiency disease caused by impaired phagocytic function. Hematopoietic stem cell transplantation (HSCT) is a definitive cure for CGD; however, the use of HSCT is limited because of associated problems, including transplantation-related mortali...

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Detalles Bibliográficos
Autores principales: Ju, Hee Young, Kang, Hyoung Jin, Hong, Che Ry, Lee, Ji Won, Kim, Hyery, Song, Sang Hoon, Yu, Kyung-Sang, Jang, In-Jin, Park, June Dong, Park, Kyung Duk, Shin, Hee Young, Kim, Joong-Gon, Ahn, Hyo Seop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5177714/
https://www.ncbi.nlm.nih.gov/pubmed/28018447
http://dx.doi.org/10.3345/kjp.2016.59.11.S57
Descripción
Sumario:Chronic granulomatous disease (CGD) is a primary immunodeficiency disease caused by impaired phagocytic function. Hematopoietic stem cell transplantation (HSCT) is a definitive cure for CGD; however, the use of HSCT is limited because of associated problems, including transplantation-related mortality and engraftment failure. We report a case of a patient with CGD who underwent successful HSCT following a targeted busulfan and fludarabine reduced-toxicity myeloablative conditioning. Intravenous busulfan was administered once daily for 4 consecutive days (days –8 to –5), and the target area under the curve was 75,000 µg·hr/L. Fludarabine (40 mg/m(2)) was administered once daily for 6 consecutive days from days –8 to –3. Antithymocyte globulin (2.5 mg/kg/day) was administered from days –4 to –2. The patient underwent successful engraftment and did not have any severe toxicity related to the transplantation. Conditioning with a targeted busulfan and fludarabine regimen could provide a better outcome for HSCT in CGD, with close regulation of the busulfan dose.