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dc.contributor.author문영철*
dc.date.accessioned2022-02-22T16:31:25Z-
dc.date.available2022-02-22T16:31:25Z-
dc.date.issued2021*
dc.identifier.issn2044-5385*
dc.identifier.otherOAK-30700*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/260670-
dc.description.abstractIn multiple myeloma (MM), a high number of focal lesions (FL) detected using positron emission tomography/computed tomography (PET/CT) was found to be associated with adverse prognosis. To design a new risk stratification system that combines the Revised International Staging System (R-ISS) with FL, we analyzed the data of 380 patients with newly diagnosed MM (NDMM) who underwent F-18-fluorodeoxyglucose (F-18-FDG) PET/CT upon diagnosis. The K-adaptive partitioning algorithm was adopted to define subgroups with homogeneous survival. The combined R-ISS with PET/CT classified NDMM patients into four groups: R-ISS/PET stage I (n = 31; R-ISS I with FL <= 3), stage II (n = 156; R-ISS I with FL > 3 and R-ISS II with FL <= 3), stage III (n = 162; R-ISS II with FL > 3 and R-ISS III with FL <= 3), and stage IV (n = 31; R-ISS III with FL > 3). The 2-year overall survival rates for stages I, II, III, and IV were 96.7%, 89.8%, 74.7%, and 50.3%. The 2-year progression-free survival rates were 84.1%, 64.7%, 40.8%, and 17.1%, respectively. The new R-ISS/PET was successfully validated in an external cohort. This new system had a remarkable prognostic power for estimating the survival outcomes of patients with NDMM. This system helps discriminate patients with a good prognosis from those with a poor prognosis more precisely.*
dc.languageEnglish*
dc.publisherSPRINGERNATURE*
dc.titleDevelopment of a new risk stratification system for patients with newly diagnosed multiple myeloma using R-ISS and F-18-FDG PET/CT*
dc.typeArticle*
dc.relation.issue12*
dc.relation.volume11*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.journaltitleBLOOD CANCER JOURNAL*
dc.identifier.doi10.1038/s41408-021-00577-2*
dc.identifier.wosidWOS:000724755600002*
dc.identifier.scopusid2-s2.0-85120408632*
dc.author.googleCho, Hee Jeong*
dc.author.googleJung, Sung-Hoon*
dc.author.googleJo, Jae-Cheol*
dc.author.googleLee, Yoo Jin*
dc.author.googleYoon, Sang Eun*
dc.author.googlePark, Sung-Soo*
dc.author.googleKim, Do Young*
dc.author.googleShin, Ho-Jin*
dc.author.googleMun, Yeung-Chul*
dc.author.googleYi, Jun Ho*
dc.author.googleKim, Hyo Jung*
dc.author.googleKim, Da Jung*
dc.author.googleLee, Ho Sup*
dc.author.googleBae, Sung Hwa*
dc.author.googleHong, Chae Moon*
dc.author.googleJeong, Shin Young*
dc.author.googleMin, Jung-Joon*
dc.author.googleSohn, Sang Kyun*
dc.author.googleMin, Chang-Ki*
dc.author.googleKim, Kihyun*
dc.author.googleLee, Je-Jung*
dc.author.googleMoon, Joon Ho|Korean Multiple Myeloma Workin*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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의과대학 > 의학과 > Journal papers
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