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Combination of clofarabine, cyclophosphamide, and etoposide for relapsed or refractory childhood and adolescent acute myeloid leukemia.
- Source :
-
Pediatric hematology and oncology [Pediatr Hematol Oncol] 2017 May; Vol. 34 (4), pp. 187-198. Date of Electronic Publication: 2017 Oct 17. - Publication Year :
- 2017
-
Abstract
- Relapsed/refractory acute myeloid leukemia (AML) has an extremely poor prognosis. We describe 17 children and adolescents with relapsed/refractory AML who received clofarabine, cyclophosphamide, and etoposide. Seven patients (41%) responded: 4 with a complete response (CR); 1 with CR with incomplete platelet recovery; and 2 with a partial response. Additionally, 4 developed hypocellular marrow without evidence of leukemia; 5 patients had resistant disease; and 1 suffered early toxic death. After further therapy including transplantation, 4 patients (24%) are alive without evidence of disease at a median of 60 months. This anthracycline-free regimen may be studied for relapsed or refractory AML, but due to the high risk of marrow aplasia reduced doses of clofarabine and cyclophosphamide should be used.
- Subjects :
- Adenine Nucleotides administration & dosage
Adenine Nucleotides adverse effects
Adolescent
Adult
Allografts
Antineoplastic Combined Chemotherapy Protocols adverse effects
Arabinonucleosides administration & dosage
Arabinonucleosides adverse effects
Child
Child, Preschool
Clofarabine
Cyclophosphamide administration & dosage
Cyclophosphamide adverse effects
Disease-Free Survival
Etoposide administration & dosage
Etoposide adverse effects
Female
Follow-Up Studies
Hematopoietic Stem Cell Transplantation
Humans
Infant
Male
Survival Rate
Antineoplastic Combined Chemotherapy Protocols administration & dosage
Leukemia, Myeloid, Acute mortality
Leukemia, Myeloid, Acute therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1521-0669
- Volume :
- 34
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Pediatric hematology and oncology
- Publication Type :
- Academic Journal
- Accession number :
- 29039989
- Full Text :
- https://doi.org/10.1080/08880018.2017.1360970