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Allogeneic hematopoietic cell transplantation in chemotherapy-induced aplasia in children with high-risk acute myeloid leukemia or myelodysplasia
- Source :
- Pediatric Blood & Cancer. 66:e27481
- Publication Year :
- 2018
- Publisher :
- Wiley, 2018.
-
Abstract
- Relapse remains the most common cause of treatment failure after hematopoietic cell transplantation for acute myeloid leukemia. Inability to achieve hematologic complete remission has been a barrier to transplant for patients with refractory disease. We describe six children with refractory myeloid disease undergoing transplant in chemotherapy-induced aplasia, as a strategy to facilitate curative therapy in refractory patients. Clofarabine- or high-dose cytarabine-based chemotherapy regimens were used to achieve marrow aplasia, followed by reduced-intensity conditioning and allogeneic transplant before hematologic recovery. Long-term disease control was achieved in five, with one transplant-related mortality, suggesting the feasibility of this approach.
- Subjects :
- Male
Oncology
medicine.medical_specialty
Transplantation Conditioning
Myeloid
Adolescent
medicine.medical_treatment
Graft vs Host Disease
Red-Cell Aplasia, Pure
03 medical and health sciences
0302 clinical medicine
Refractory
hemic and lymphatic diseases
Internal medicine
Antineoplastic Combined Chemotherapy Protocols
medicine
Humans
Transplantation, Homologous
Clofarabine
Child
Retrospective Studies
Chemotherapy
business.industry
Cytarabine
Hematopoietic Stem Cell Transplantation
Myeloid leukemia
Hematology
Aplasia
Prognosis
medicine.disease
Transplantation
Leukemia, Myeloid, Acute
medicine.anatomical_structure
Child, Preschool
Myelodysplastic Syndromes
030220 oncology & carcinogenesis
Pediatrics, Perinatology and Child Health
Female
Neoplasm Recurrence, Local
business
Vidarabine
Follow-Up Studies
030215 immunology
medicine.drug
Subjects
Details
- ISSN :
- 15455009
- Volume :
- 66
- Database :
- OpenAIRE
- Journal :
- Pediatric Blood & Cancer
- Accession number :
- edsair.doi.dedup.....a7b6f484a3cc3be354e324703d2275ff
- Full Text :
- https://doi.org/10.1002/pbc.27481