Myeloproliferative neoplasms treated with hydroxyurea, pegylated interferon alpha-2A or ruxolitinib: clinicohematologic responses, quality-of-life changes and safety in the real-world setting

HEMATOLOGY(2020)

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Abstract
Introduction:Real-world data of responses, quality-of-life (QOL) changes and adverse events in patients with myeloproliferative neoplasms (MPN) on conventional therapy (hydroxyurea +/- anagrelide), pegylated interferon alpha-2A (PEG-IFN alpha-2A) or ruxolitinib are limited. Methods:We prospectively studied MPN patients receiving conventional therapy, PEG-IFN alpha-2A or ruxolitinib. Next-generation sequencing of 69 myeloid-related genes was performed. Clinicohematologic responses, adverse events, and QOL (determined by the Myeloproliferative Neoplasm Symptom Assessment Form Total Symptom Score, MPN-SAF TSS) were evaluated. Results:Seventy men and fifty-five women with polycythemia vera (PV) (N = 23), essential thrombocythemia (ET) (N = 56) and myelofibrosis (MF) (N = 46) were studied for a median of 36 (range: 19-42) months. In PV, responses were comparable for different modalities.CREBBPmutations were associated with inferior responses. In ET, PEG-IFN alpha-2A resulted in superior clinicohematologic complete responses (CHCR) (P = 0.045). In MF, superior overall response rates (ORR) were associated with ruxolintib (P = 0.018) andJAK2V617F mutation (P = 0.04). For the whole cohort, ruxolitinib led to rapid and sustained reduction in spleen size within the first 6 months, and significant improvement of QOL as reflected by reduction in MPN-SAF TSS (P < 0.001). Adverse events of grades 1-2 were observed in 44%, 62% and 20% of patients receiving conventional therapy, PEG-IFN alpha-2A and ruxolitinib respectively; and of grade 3-4 in 7% and 9% of patients receiving PEG-IFN alpha-2A and ruxolitinib. Conclusions:Conventional therapy, PEG-IFN alpha-2A and ruxolitinib induced responses in all MPN subtypes. PEG-IFN alpha-2A led to superior CHCR in ET; whereas ruxolitinib resulted in superior ORR in MF, and significant reduction in spleen size and improvement in QOL.
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Key words
Myeloproliferative neoplasms,polycythemia vera,essential thrombocythemia,primary myelofibrosis,hydroxyurea,anagrelide,interferon,ruxolitinib
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