Abstract
BACKGROUND: The clinical significance of protein tyrosine phosphatase nonreceptor type 11 mutation (PTPN11(mut) ) in acute myeloid leukemia (AML) is underestimated. METHODS: We collected the data of AML patients with mutated PTPN11 and wild-type PTPN11 (PTPN11(wt) ) treated at our hospital and analyzed their clinical characteristics and prognosis. RESULTS: Fifty-nine PTPN11(mut) and 124 PTPN11(wt) AML patients were included. PTPN11(mut) was more common in myelomonocytic and monocytic leukemia, and was more likely to co-mutate with KRAS, KMT2C, NRAS, U2AF1, NOTCH1, IKZF1, and USH2A mutations than PTPN11(wt) . The overall survival for AML patients with PTPN11(mut) was significantly shorter than that for those with PTPN11(wt) (p = 0.03). The negative impact of PTPN11(mut) on overall survival was pronounced in the "favorable" and "intermediate" groups of ELN2017 risk stratification, as well as in the wild-type NPM1 group (p = 0.01, p = 0.01, and p = 0.04). CONCLUSION: PTPN11(mut) is associated with distinct clinical and molecular characteristics, and adverse prognosis in AML patients.