Abstract
Chronic myeloid leukemia (CML) is not a common pathology in childhood, representing 2-3% of leukemia in children and adolescents with an incidence of 0.6 to 1.2 / million children / year that increases with the age.
The clinical characteristics are different in this population, compared to adults, tending to present
more aggressive characteristics (greater white blood cell count, greater spleen size in proportion to body
size, higher frequency of advanced stages in diagnosis); show a distribution of BCR-ABL1 breakpoints
that resemble adult acute lymphoblastic leukemia with positive Philadelphia chromosome, and have a higher proportion of mutated cancer driver genes.
With the appearance of tyrosine kinase inhibitors (ITK), the prognosis of this disease has changed, with a life expectancy in adult patients almost identical to that of a healthy population of the same age.
There is no protocol in Argentina aimed exclusively at pediatric patients. Nor do we have an dequate registry in our country, and each professional follows the guidelines of different adult patient guides.
The objective of this work is to initiate a national registry with data of our patients and in this way evaluate the characteristics of this population, allowing in the future the creation of guidelines for the diagnosis, management, treatment and monitoring of these patients.
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