The effects of mutational profiles on phenotypic presentation of myeloproliferative neoplasm subtypes in Bosnia: 18 year follow-up

摘要

The identification of mutually exclusive somatic mutations shared among myeloproliferative neoplasm (MPN) subtypes has provided a powerful tool for studying disease evolution. Clinical features, gene mutations, and survival over 18 years were analyzed in MPN patients. One hundred thirty-eight MPN patients were subcategorized according to MPN subtypes: essential thrombocythemia (ET, n = 41), polycythemia vera (PV, n = 56), primary myelofibrosis (PMF, n = 10), and MPN unclassified (MPN-U, n = 31). Patient characteristics included clinical parameters, overall survival (OS), and mutational status of the Janus kinase 2 ( ), calreticulin ( ), and myeloproliferative leukemia virus oncogene ( ) genes. We compared hematologic and clinical features of -ET vs. CALR-mutated ET vs. -PV patients. -patients had higher values of erythrocytes, hemoglobin, and hematocrit compared to -mutated patients ( < 0.05). The mutant allele burden in -PV and -ET patients directly correlated with erythrocyte, hemoglobin, and hematocrit values, but it inversely correlated with platelet count. Thus, mutant allele burden was an indicator of the clinical phenotype in -MPN patients. OS was not affected by the mutational status. In general, mutated , , and genes left specific hematological signatures.