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Usefulness of spleen volume measured by computed tomography for predicting clinical outcome in primary myelofibrosis

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dc.contributor.authorSong, Moo-Kon-
dc.contributor.authorChung, Joo-Seop-
dc.contributor.authorLim, Sung-Nam-
dc.contributor.authorLee, Gyeong-won-
dc.contributor.authorLee, Sang-Min-
dc.contributor.authorLee, Nam-Kyung-
dc.contributor.authorChoi, Jae-Cheol-
dc.contributor.authorOh, So-Yeon-
dc.date.accessioned2022-07-15T05:37:49Z-
dc.date.available2022-07-15T05:37:49Z-
dc.date.created2021-05-12-
dc.date.issued2016-10-
dc.identifier.issn0925-5710-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153869-
dc.description.abstractAlthough splenomegaly is major characteristic of primary myelofibrosis (PMF), splenomegaly has been devalued due to a less reliable method based on physical examination (PEx). We evaluated whether spleen volume (SV) on CT would accurately predict clinical outcomes in PMF. A total of 188 patients were enrolled. SV was quantitated by the automatic volume software. In ROC curve, the SV predicted prognosis more accurately than spleen length by PEx (p < 0.001). The ideal cut-off value was 378.1 cm3 for SV, which was divided into high- and low-volume status. Patients with low SV status had superior leukemia-free survival and overall survival compared to high SV status (p < 0.001, p < 0.001) In the Cox analysis, old age ≥65 years (p = 0.004, p = 0.001), low Hemoglobin <10.0 g/dL (p = 0.023, p = 0.021), high WBC counts ≥25 × 109/L (p = 0.003, p = 0.006), peripheral blasts ≥1 % (p = 0.029, p = 0.020), unfavorable cytogenetic abnormalities (p = 0.025, p = 0.028), and high SV status (p = 0.004, p = 0.003) were independently associated with survivals. SV measured by CT was important for predicting survival in patients with PMF.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER JAPAN KK-
dc.titleUsefulness of spleen volume measured by computed tomography for predicting clinical outcome in primary myelofibrosis-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Moo-Kon-
dc.identifier.doi10.1007/s12185-016-2050-y-
dc.identifier.scopusid2-s2.0-84976334740-
dc.identifier.wosid000385153200011-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF HEMATOLOGY, v.104, no.4, pp.476 - 484-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF HEMATOLOGY-
dc.citation.titleINTERNATIONAL JOURNAL OF HEMATOLOGY-
dc.citation.volume104-
dc.citation.number4-
dc.citation.startPage476-
dc.citation.endPage484-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaHematology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.subject.keywordPlusAGNOGENIC MYELOID METAPLASIA-
dc.subject.keywordPlusCYTOGENETIC-RISK CATEGORIZATION-
dc.subject.keywordPlusINTERNATIONAL WORKING GROUP-
dc.subject.keywordPlusPROGNOSTIC SCORING SYSTEM-
dc.subject.keywordPlusWORLD-HEALTH-ORGANIZATION-
dc.subject.keywordPlusESSENTIAL THROMBOCYTHEMIA-
dc.subject.keywordPlusIDIOPATHIC MYELOFIBROSIS-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordAuthorPrimary myelofibrosis-
dc.subject.keywordAuthorSplenomegaly-
dc.subject.keywordAuthorComputed tomography-
dc.subject.keywordAuthorSplenic volume-
dc.subject.keywordAuthorOverall survival-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs12185-016-2050-y-
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