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dc.contributor.author문영철*
dc.date.accessioned2022-08-12T16:31:10Z-
dc.date.available2022-08-12T16:31:10Z-
dc.date.issued2022*
dc.identifier.issn2152-2650*
dc.identifier.issn2152-2669*
dc.identifier.otherOAK-32185*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/262343-
dc.description.abstractWe evaluated the treatment outcome of ruxolitinib, especially focused on RBC TF and anemia in 123 MF patients in a real-world setting. Approximately one-third showed long-term and severe transfusion dependence, respectively. In addition, the presence of MF-related anemia was a risk factor for predicting RBC TF dependency throughout the ruxolitinib treatment. Given these data, patients with = 2 units of RBC TF over eight weeks at the time of ruxolitinib initiation need more supportive care with awareness of the risk of anemia in actual practice. Introduction/Background: Ruxolitinib is an established treatment for myelofibrosis (MF) that has demonstrated clinical benefit by reducing spleen size and debilitating MF-related symptoms. However, despite the efficacy of ruxolitinib, anemia remains a major adverse event that causes dose modification or discontinuation in real-world practice. Additionally, dependence on red blood cell (RBC) transfusion (TF) is common during treatment; therefore, we explored the outcome of ruxolitinib therapy with a primary focus on RBC TF. Patients/Methods: We retrospectively reviewed the medical records of 123 MF patients treated with ruxolitinib between January 2012 and April 2020 at eight academic centers in Korea. Results: At ruxolitinib initiation, 38 patients (30.9%) underwent >= 2 units of RBC TF over 8 weeks. The most common reason for permanent discontinuation was intolerant anemia (10/63, 15.9%). The most common reasons for temporary interruption were nonhematologic toxicity (26/55, 21.1%), anemia (23/55, 18.7%) and thrombocytopenia (13/55, 10.6%). Among the 123 patients in the study, 57 (46.3%), 42 (34.1%), and 40 patients (32.5%) who were receiving or stopped ruxolitinib therapy had a status of RBC TF dependence, long-term RBC TF dependence, or severe RBC TF dependence, respectively. The presence of = 2 units of RBC transfusion over 8 weeks at ruxolitinib initiation was an independent risk factor for persistent RBC TF dependence. Conclusion: The requirement for RBC TF is commonly encountered during treatment of MF with ruxolitinib, particularly among those with pre-existing = 2 units of RBC TF over 8 weeks. For those patients, overcoming the barrier of maintenance TF is demanding.*
dc.languageEnglish*
dc.publisherCIG MEDIA GROUP, LP*
dc.subjectAnemia*
dc.subjectRed Blood Cell Transfusion*
dc.subjectMyelofibrosis*
dc.subjectRuxolitinib*
dc.subjectTransfusion*
dc.titleReal-World Outcomes of Ruxolitinib in Patients With Myelofibrosis Focusing on Red Blood Cell Transfusion: A Multicenter Study From the MPN Working Party of the Korean Society of Hematology*
dc.typeArticle*
dc.relation.issue10*
dc.relation.volume22*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpageE931*
dc.relation.lastpageE937*
dc.relation.journaltitleCLINICAL LYMPHOMA MYELOMA & LEUKEMIA*
dc.identifier.doi10.1016/j.clml.2022.06.008*
dc.identifier.wosidWOS:000903822700007*
dc.identifier.scopusid2-s2.0-85134617475*
dc.author.googleJung, Eun Hee*
dc.author.googleHong, Junshik*
dc.author.googleKim, Sung-Yong*
dc.author.googlePark, Young*
dc.author.googleYuh, Young Jin*
dc.author.googleMun, Yeung-Chul*
dc.author.googleLee, Won-Sik*
dc.author.googlePark, Sung-Kyu*
dc.author.googleBang, Soo Mee*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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의과대학 > 의학과 > Journal papers
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