{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,4]],"date-time":"2026-06-04T13:52:22Z","timestamp":1780581142774,"version":"3.54.1"},"reference-count":26,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2018,1,17]],"date-time":"2018-01-17T00:00:00Z","timestamp":1516147200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100000054","name":"National Cancer Institute","doi-asserted-by":"publisher","award":["CA016672"],"award-info":[{"award-number":["CA016672"]}],"id":[{"id":"10.13039\/100000054","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European J of Haematology"],"published-print":{"date-parts":[[2018,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Severe thrombocytopenia (platelets &lt;50\u00a0\u00d7\u00a010<jats:sup>9<\/jats:sup>\/L) is associated with very poor outcome of patients with myelofibrosis (<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>). As patients with primary myelofibrosis (<jats:styled-content style=\"fixed-case\">PMF<\/jats:styled-content>) differ from patients with postessential thrombocythemia (<jats:styled-content style=\"fixed-case\">PET<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>) and postpolycythemia vera myelofibrosis (<jats:styled-content style=\"fixed-case\">PPV<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>), we aimed to evaluate the significance of low platelets among these patients. We present clinical characteristics and outcome of patients with either <jats:styled-content style=\"fixed-case\">PMF<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> PPV<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>, or <jats:styled-content style=\"fixed-case\">PET<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>, and thrombocytopenia who presented to our institution between 1984 and 2015. Of 1269 patients (877 <jats:styled-content style=\"fixed-case\">PMF<\/jats:styled-content>, 212 <jats:styled-content style=\"fixed-case\">PPV<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>, 180 <jats:styled-content style=\"fixed-case\">PET<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>), 11% and 14% had platelets either &lt;50\u00a0\u00d7\u00a010<jats:sup>9<\/jats:sup>\/L or between 50\u2010100\u00a0\u00d7\u00a010<jats:sup>9<\/jats:sup>\/L, respectively. Patients with platelets &lt;50\u00a0\u00d7\u00a010<jats:sup>9<\/jats:sup>\/L were most anemic and transfusion dependent, had highest blast count and unfavorable karyotype. In general, their overall and leukemia\u2010free survival was the shortest with median time of 15 and 13\u00a0months, respectively; with incidence of acute leukemia almost twice as high as in the remaining patients (6.9 vs 3.6 cases per 100 person\u2010years). Nevertheless, this observation remains mostly significant for patients with <jats:styled-content style=\"fixed-case\">PMF<\/jats:styled-content>, as those with <jats:styled-content style=\"fixed-case\">PEV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">PVT<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> have already significantly inferior prognosis with platelets &lt;100\u00a0\u00d7\u00a010<jats:sup>9<\/jats:sup>\/L.<\/jats:p>","DOI":"10.1111\/ejh.13005","type":"journal-article","created":{"date-parts":[[2017,12,11]],"date-time":"2017-12-11T07:46:49Z","timestamp":1512978409000},"page":"257-263","source":"Crossref","is-referenced-by-count":56,"title":["Significance of thrombocytopenia in patients with primary and postessential thrombocythemia\/polycythemia vera myelofibrosis"],"prefix":"10.1111","volume":"100","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6624-4196","authenticated-orcid":false,"given":"Lucia","family":"Masarova","sequence":"first","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4669-0233","authenticated-orcid":false,"given":"Ahmad","family":"Alhuraiji","sequence":"additional","affiliation":[{"name":"Kuwait Cancer Control Center  Shuwaikh Kuwait"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Prithviraj","family":"Bose","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naval","family":"Daver","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naveen","family":"Pemmaraju","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jorge","family":"Cortes","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sherry","family":"Pierce","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hagop","family":"Kantarjian","sequence":"additional","affiliation":[{"name":"Department of Leukemia University of Texas MD Anderson Cancer Center  Houston TX 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