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Original Articles: Clinical

MPN10 score and survival of molecularly annotated myeloproliferative neoplasm patients

, , , , , , , , , , , , , , & show all
Pages 844-854 | Received 04 May 2017, Accepted 29 Jul 2017, Published online: 22 Aug 2017
 

Abstract

JAK2, CALR, MPL and triple-negative mutational status has a direct impact on symptom severity and disease burden assessed by MPN10 score in myeloproliferative neoplasms (MPNs). Among 93 patients; median MPN10 score was 48 (5–76) in JAK2 mutants versus 25 (4–80) in JAK2 negative (p < .001); 22.5 (4–65) in CALR mutants versus 35 (5–80) in CALR negative (p < .050) and 21 (10–48) in triple negative versus 40 (4–80) in JAK2/CALR/MPL mutants (p < .001). At three years, progression free and overall survival of JAK2-positive versus JAK2-negative patients were 62% versus 100% (p < .001); 85% versus 100% (p = .011) and were 100% versus 78% (p = .067); 100% versus 92% (p = .197) in CALR-positive versus CALR-negative patients and 100% versus 75% (p = .004); 100% versus 90% (p = .015) in triple negative versus mutant patients, respectively. MPN10 score in association with driver gene mutations can be used as a predictor of survival in MPN patients.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at https://doi.org/10.1080/10428194.2017.1365852.

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