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Chronic Myeloid Leukemia with e19a2BCR-ABL1Transcripts and Marked Thrombocytosis: The Role of Molecular Monitoring
Author(s) -
Stephen E. Langabeer,
Sarah L. McCarron,
Johanna Kelly,
Janusz Krawczyk,
Suzanne McPherson,
Kanthi Perera,
Philip Murphy
Publication year - 2012
Publication title -
case reports in hematology
Language(s) - English
Resource type - Journals
eISSN - 2090-6560
pISSN - 2090-6579
DOI - 10.1155/2012/458716
Subject(s) - thrombocytosis , myeloid leukemia , medicine , tyrosine kinase , tyrosine kinase inhibitor , breakpoint cluster region , cancer research , oncology , immunology , platelet , receptor , cancer
While most patients with chronic myeloid leukemia (CML) express either e13a2 or e14a2 BCR-ABL1 transcripts, a significant minority expresses variant transcripts, of which e19a2 is the most common. Although considered to have a relatively favourable outcome, reported responses to tyrosine kinase inhibitor (TKI) therapy are variable with molecular monitoring in CML patients with e19a2 BCR-ABL1 transcripts rarely reported. A case of e19a2 BCR-ABL1 CML with marked thrombocytosis is described in which the value of molecular monitoring is emphasised during treatment interruptions, dose reductions, and changes. This case serves to demonstrate the requirement for prospective real-time quantitative PCR (RQ-PCR) assays for patients with variant BCR-ABL1 transcript types and standardisation of such assays to enable modern patient management.

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