{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,12]],"date-time":"2026-04-12T12:10:17Z","timestamp":1775995817238,"version":"3.50.1"},"reference-count":27,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2015,4,21]],"date-time":"2015-04-21T00:00:00Z","timestamp":1429574400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European J of Haematology"],"published-print":{"date-parts":[[2016,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Nucleophosmin (<jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic>) mutations in chronic myelomonocytic leukemia (<jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content>) are extremely uncommon, and the clinicopathologic features of these neoplasms are poorly characterized. Over a 10\u2010yr interval, <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutation analysis was performed in 152 <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content> at our institution. <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutations were identified in 8 (5.3%) patients, five men and three women, with a median age of 72\u00a0yr (range, 27\u201387). In all patients, the bone marrow was hypercellular with multilineage dysplasia, monocytosis, and retained maturation supporting a diagnosis of <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content>. <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutation allele burden was &lt;5% in two patients and &gt;10% in six patients. Four (50%) patients, all with &gt;10% <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1,<\/jats:italic> progressed <jats:styled-content style=\"fixed-case\">AML<\/jats:styled-content> with a median interval of 11\u00a0months (range, 1\u201321). Compared with 144 <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content> without <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutations, <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content> patients with <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutation presented with more severe anemia (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.053), higher <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content> monocyte percentage (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.033), and an increased tendency for <jats:styled-content style=\"fixed-case\">AML<\/jats:styled-content> progression (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.088) and an inferior overall survival (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.076). Mutations involving <jats:italic><jats:styled-content style=\"fixed-case\">NRAS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">KRAS<\/jats:styled-content> (2\/7), <jats:styled-content style=\"fixed-case\">TET<\/jats:styled-content>2(2\/5), <jats:styled-content style=\"fixed-case\">ASXL<\/jats:styled-content>1(1\/5,) and <jats:styled-content style=\"fixed-case\">FLT<\/jats:styled-content>3(0\/8)<\/jats:italic> were not significantly different between these two groups. In summary, <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content> with <jats:italic><jats:styled-content style=\"fixed-case\">NPM<\/jats:styled-content>1<\/jats:italic> mutation shows histopathological features of <jats:styled-content style=\"fixed-case\">CMML<\/jats:styled-content>, but patients appear to have a high probability for <jats:styled-content style=\"fixed-case\">AML<\/jats:styled-content> progression and may require aggressive clinical intervention, especially in patients with a high mutation burden.<\/jats:p>","DOI":"10.1111\/ejh.12549","type":"journal-article","created":{"date-parts":[[2015,3,24]],"date-time":"2015-03-24T21:37:46Z","timestamp":1427233066000},"page":"65-71","source":"Crossref","is-referenced-by-count":49,"title":["Chronic myelomonocytic leukemia with nucleophosmin (<i><scp>NPM<\/scp>1<\/i>) mutation"],"prefix":"10.1111","volume":"96","author":[{"given":"Jie","family":"Peng","sequence":"first","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"},{"name":"Department of Hematology Central South University Xiangya Hospital Changsha China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhuang","family":"Zuo","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bin","family":"Fu","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"},{"name":"Department of Hematology Central South University Xiangya Hospital Changsha China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasuhiro","family":"Oki","sequence":"additional","affiliation":[{"name":"Department of Lymphoma\/Myeloma The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Guilin","family":"Tang","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maitrayee","family":"Goswami","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Priyanka","family":"Priyanka","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tariq","family":"Muzzafar","sequence":"additional","affiliation":[{"name":"Department of Hematopathology The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L. 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