Juvenile myelomonocytic leukemia.

Charlotte Marie Niemeyer, Christian Kratz
Author Information
  1. Charlotte Marie Niemeyer: Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, University of Freiburg, Mathildenstrasse 1, 79106 Freiburg, Germany. Niemeyer@kikli.ukl.uni-freiburg.de

Abstract

Juvenile myelomonocytic leukemia is an aggressive neoplasia of early childhood. Only allogeneic stem cell transplantation (SCT) offers long-term cure. In the absence of an HLA-matched family donor, early SCT from an unrelated donor is the treatment of choice for most children. With clear evidence of a graft-versus-leukemia effect and a high post-transplant relapse rate, the outcome of SCT depends, in part, on the management of immunosuppression during the procedure. The impact of pretransplant cytoreductive treatment, such as intensive chemotherapy, splenectomy, or 13-cis retinoic acid, is unclear. Hypersensitivity for granulocyte-macrophage colony-stimulating factor and pathologic activation of the Ras/MAPK pathway play an important role in the pathophysiology of juvenile myelomonocytic leukemia and provide the opportunity for several novel therapeutic approaches.

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MeSH Term

Child, Preschool
Chromosome Disorders
Gene Expression Regulation, Leukemic
Graft vs Leukemia Effect
Granulocyte-Macrophage Colony-Stimulating Factor
Histocompatibility
Humans
Infant
Leukemia, Myelomonocytic, Chronic
Leukocyte Count
Recurrence
Stem Cell Transplantation

Chemicals

Granulocyte-Macrophage Colony-Stimulating Factor

Word Cloud

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