AI Article Synopsis

  • - Chronic myeloid leukemia (CML) is rare in children, but treatment with tyrosine kinase inhibitors (TKI) has shown excellent survival rates, with all patients in the study responding positively within 20 to 68 days of starting treatment.
  • - A review of 15 pediatric patients treated from 1997 to 2022 revealed that 100% of them survived, with significant responses seen within 6 months for some, and a median follow-up of 79 months.
  • - The study suggests that while most patients can maintain remission and continue TKI treatment for several years, some can safely stop the medication without experiencing a relapse, indicating a promising outlook for children with chronic phase CML.

Article Abstract

Chronic myeloid leukemia (CML) is very rare during childhood. Tyrosine kinase inhibitors (TKI) provide very good results in terms of survival. The medical records of 15 chronic phase (CP)-CML patients in a university hospital pediatric hematology department between 1997 and 2022 were reviewed retrospectively. Complete hematological response was documented in all patients between 20 and 68 (median 30) days of treatment. Major molecular response was achieved in seven patients within 6 months. Median follow-up for the study group was 79 (range 3-330) months and overall survival was 100%. Three patients (2 blastic transformation, 1 therapy resistant) underwent bone marrow transplantation (BMT) and one with blastic transformation is scheduled to undergo BMT. TKI were discontinued in three patients after a median of 86 (range 73-177) months. The complete molecular remission maintenance period before discontinuation of TKI was 81 (range 62-122) months. While no molecular relapse was seen before the last follow-up, the median overall follow-up period was 152 (range 131-300) months. In conclusion, recent advances have led to a very good prognosis for children with CP-CML. With TKI treatment, most patients continue their lives without disease progression. Additionally, in selected patients TKI can be discontinued without molecular relapse.

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Source
http://dx.doi.org/10.1007/s12185-022-03497-4DOI Listing

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