Abstract
We studied non-driver mutations in 62 subjects with myeloproliferative neoplasm (MPN)-associated myelofibrosis upon diagnosis, including 45 subjects with primary myelofibrosis (PMF) and 17 with post-polycythemia vera or post-essential thrombocythemia myelofibrosis (post-PV/ET MF). Fifty-eight subjects had ≥1 non-driver mutation upon diagnosis. Mutations in mRNA splicing genes, especially in U2AF1, were significantly more frequent in PMF than in post-PV/ET MF (33 vs. 6%; P = 0.015). There were also striking differences in clonal architecture. These data indicate different genomic spectrums between PMF and post-PV/ET MF.
Original language | English (US) |
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Article number | 99 |
Journal | Journal of Hematology and Oncology |
Volume | 10 |
Issue number | 1 |
DOIs | |
State | Published - May 2 2017 |
Externally published | Yes |
Keywords
- Myeloproliferative neoplasm-associated myelofibrosis
- Non-driver mutation
- Targeted gene sequencing
ASJC Scopus subject areas
- Molecular Biology
- Hematology
- Oncology
- Cancer Research