Abstract |
Hematopoietic stem cell transplant (HSCT) is the only curative treatment modality for Wiskott-Aldrich syndrome. Haploidentical HSCT with posttransplant cyclophosphamide (PTCy) is an upcoming option in children with nonmalignant conditions. However, only few cases have been reported for Wiskott-Aldrich syndrome HSCT with PTCy approach. Here we report a 4-year-old boy, treated successfully by haploidentical HSCT with myeloablative conditioning ( busulfan, fludarabine, and thiotepa) and PTCy. Posttransplant chimerism was fully donor. Of 13 cases (current case and other 12 published cases) 10 are alive and disease free after haploidentical HSCT with PTCy. Haploidentical HSCT with PTCy using myeloablative conditioning is feasible and safe.
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Authors | Anil Sharma, Neha Rastogi, Rohit Kapoor, Goutomi Chatterjee, Satya P Yadav |
Journal | Journal of pediatric hematology/oncology
(J Pediatr Hematol Oncol)
Vol. 43
Issue 2
Pg. e230-e233
(03 01 2021)
ISSN: 1536-3678 [Electronic] United States |
PMID | 32459721
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved. |
Chemical References |
- Myeloablative Agonists
- Cyclophosphamide
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Topics |
- Child, Preschool
- Combined Modality Therapy
- Cyclophosphamide
(therapeutic use)
- Hematopoietic Stem Cell Transplantation
(methods)
- Humans
- Male
- Myeloablative Agonists
(therapeutic use)
- Prognosis
- Tissue Donors
- Transplantation Conditioning
(methods)
- Transplantation, Haploidentical
(methods)
- Wiskott-Aldrich Syndrome
(pathology, therapy)
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