EVI1 expression predicts outcome in higher-risk myelodysplastic syndrome patients

Abstract

The clinical impact of ecotropic viral integration site 1 (EVI1) expression status in myelodysplastic syndromes (MDS) is poorly defined. Here, we investigate the expression of EVI1 and its associated clinical and cytogenetic characteristics in 398 MDS patients. High EVI1 levels (EVI1^high) were found more frequently in Higher-risk MDS patients. Other cytogenetic abnormalities over-represented among EVI1^high cases included complex karyotype, del(5q), monosomy 7, and 12q-compared with EVI1^low MDS. No specific gene mutation was found different between EVI1^high and EVI1^low patients, except for a high proportion of TP53 mutation in the EVI1^high group. For EVI^high patients, mean number of gene mutations was higher than that in EVI1^low patients. No definite correlation was found between EVI1 expression and MDS prognosis. However, for Higher-risk MDS patients, EVI1^high patients have poorer survival rate compared with EVI1^low patients. Moreover, EVI1^high was an adverse prognostic marker for MDS with excess blasts subtype. The addition of EVI1 could deteriorate the survival of MDS patients with chromosome 3 abnormalities, del(5q-) or monosomy 7. Taken together, EVI1 overexpression is a poor prognostic marker for higher-risk MDS group and could be included in risk stratification for MDS patients.

Keywords:

• EVI1
• higher-risk
• myelodysplastic syndrome
• prognostic

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments ethical standards.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at http://dx.doi.org/10.1080/10428194.2018.1459615.

Additional information

Funding

The research was funded by National Natural Science Foundation of China (81670102), Natural Science Foundation of Tianjin (16JCYBJC25200), and SKLEH-Pilot Research Grant (ZK16-03).