Epigenetic combination therapy for children with secondary myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) and concurrent solid tumor relapse Journal Article


Authors: Glasser, C. L.; Lee, A.; Eslin, D.; Marks, L.; Modak, S.; Glade Bender, J. L.
Article Title: Epigenetic combination therapy for children with secondary myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) and concurrent solid tumor relapse
Abstract: Secondary myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) is a rare but devastating complication of solid tumor treatment involving high-dose topoisomerase II inhibitor and alkylator chemotherapy. For relapsed or elderly MDS and AML patients ineligible for hematopoietic stem cell transplantation, epigenetic therapies, including DNA methyltransferase inhibitors and histone deacetylase inhibitors, have been utilized as palliative therapy, offering a well-tolerated approach to disease stabilization, prolonged survival, and quality of life. Literature on the use of epigenetic therapies for both primary and relapsed disease is scarce in the pediatric population. Here, we report 2 pediatric patients with secondary AML and MDS, respectively, due to prior therapy for metastatic solid tumors. Both patients were ineligible for hematopoietic stem cell transplantation due to concurrent solid tumor relapse, but were treated with the epigenetic combination therapy, decitabine and vorinostat, and achieved stabilization of marrow disease, outpatient palliation, and family-reported reasonable quality of life. © Copyright 2017 Wolters Kluwer Health, Inc. All rights reserved.
Keywords: solid tumor; myelodysplastic syndrome; palliative; epigenetic; acute myeloid leukemia
Journal Title: Journal of Pediatric Hematology/Oncology
Volume: 39
Issue: 7
ISSN: 1077-4114
Publisher: Lippincott Williams & Wilkins  
Date Published: 2017-10-01
Start Page: 560
End Page: 564
Language: English
DOI: 10.1097/mph.0000000000000868
PROVIDER: scopus
PUBMED: 28562519
PMCID: PMC5708164
DOI/URL:
Notes: Article -- Export Date: 1 November 2017 -- Source: Scopus
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  1. Shakeel Modak
    249 Modak