Ibrutinib-naïve chronic lymphocytic leukemia lacks Bruton tyrosine kinase mutations associated with treatment resistance
Ibrutinib-naïve chronic lymphocytic leukemia lacks Bruton tyrosine kinase mutations associated with treatment resistance
To the editor: The Bruton tyrosine kinase (BTK) inhibitor ibrutinib blocks B-cell receptor signaling via covalent binding of the BTK C481 residue.[1][1] Although ibrutinib induces durable remissions in relapsed/refractory chronic lymphocytic leukemia (CLL), a fraction of patients treated with this
Adenine, DNA Mutational Analysis, 610, Protein-Tyrosine Kinases, Leukemia, Lymphocytic, Chronic, B-Cell, Polymerase Chain Reaction, Cohort Studies, Pyrimidines, Piperidines, Drug Resistance, Neoplasm, 616, Mutation, Agammaglobulinaemia Tyrosine Kinase, Humans, Pyrazoles, Alleles
Adenine, DNA Mutational Analysis, 610, Protein-Tyrosine Kinases, Leukemia, Lymphocytic, Chronic, B-Cell, Polymerase Chain Reaction, Cohort Studies, Pyrimidines, Piperidines, Drug Resistance, Neoplasm, 616, Mutation, Agammaglobulinaemia Tyrosine Kinase, Humans, Pyrazoles, Alleles
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