Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2012 Feb 23;119(8):1821-30.
doi: 10.1182/blood-2011-10-380774. Epub 2011 Dec 30.

How I treat childhood CML

Affiliations
Case Reports

How I treat childhood CML

Jeffrey R Andolina et al. Blood. .

Abstract

Chronic myeloid leukemia (CML) is composed of 3% of pediatric leukemias, making evidence-based recommendations difficult. Imatinib has revolutionized the treatment for adult CML by eliminating allogeneic stem cell transplantation for almost all patients in chronic phase. Shown effective in pediatric CML, imatinib and successive tyrosine kinase inhibitors (TKI) have provided more therapeutic options. Because stem cell transplantation has been better tolerated in children and adolescents, the decision to treat by either TKI or transplantation is controversial. We present a recent case of a 12-month-old boy diagnosed with BCR-ABL(+) CML to highlight the controversies in treatment recommendations. We review the pediatric stem cell transplantation outcomes as well as the pediatric experience with imatinib and other TKIs. Finally, we compare the side effects as well as costs associated with allogeneic stem cell transplantation versus TKI therapy. We recommend that frontline therapy for pediatric CML in chronic phase is TKI therapy without transplantation. Patients in accelerated or blast crisis or who fail to reach landmarks on TKIs either because of intolerance or resistance should pursue stem cell transplantation. Although we recommend adopting adult clinical experience to guide therapeutic decision making, the issues of infant CML, drug formulation, pharmacokinetics, and adolescent compliance merit clinical investigation.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Flowchart for the management of pediatric CML.

Similar articles

Cited by

References

    1. Petridou ET, Sergentanis TN, Panagopoulou P, et al. In vitro fertilization and risk of childhood leukemia in Greece and Sweden. [published online ahead of print, May 25, 2011]. Pediar Blood Cancer. doi: 10.1002/pbc.23194. - DOI - PubMed
    1. Ries LAG SM, Gurney JG, Linet M, Tamra T, Young JL, Bunin GR, editors. Bethesda, MD: National Cancer Institute, SEER Program; 1999. Cancer Incidence and Survival Among Children and Adolescents: United States SEER Program 1975-1995 (NIH publication no. 99-4649).
    1. Homans AC, Young PC, Dickerman JD, Land ML. Adult-type CML in childhood: case report and review. Am J Pediatr Hematol Oncol. 1984;6(2):220–224. - PubMed
    1. Castro-Malaspina H, Schaison G, Briere J, et al. Philadelphia chromosome-positive chronic myelocytic leukemia in children: survival and prognostic factors. Cancer. 1983;52(4):721–727. - PubMed
    1. Millot F, Traore P, Guilhot J, et al. Clinical and biological features at diagnosis in 40 children with chronic myeloid leukemia. Pediatrics. 2005;116(1):140–143. - PubMed

Publication types

MeSH terms