Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/15263
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dc.contributor.authorPivkova Veljanovska, Aleksandraen_US
dc.contributor.authorGenadieva-Stavrik, Sonja Gencoen_US
dc.contributor.authorStojanoski, Zlateen_US
dc.contributor.authorChadievski, Lazaren_US
dc.contributor.authorPanovska Stavridis, Irinaen_US
dc.contributor.authorTrajkova, Sanjaen_US
dc.contributor.authorCevreska, Lidijaen_US
dc.contributor.authorGeorgievski, Borcheen_US
dc.date.accessioned2021-10-19T09:30:47Z-
dc.date.available2021-10-19T09:30:47Z-
dc.date.issued2017-05-20-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/15263-
dc.description.abstractBackground: Autologous stem cell transplantation (ASCT) improves survival in patients with myeloma and lymphoma but is associated with morbidity and nonrelapse mortality (NRM). Hematopoietic cell transplant comorbidity index (HCT-CI) was shown to predict risk of NRM and survival after allogeneic transplantation. We tested the utility of HCT-CI as a predictor of NRM and overall survival (OS) in patients undergoing ASCT. Methods: We analyzed outcomes of 220 patients after high-dose melphalan and high –dose anti lymphoma chemotherapy during year 2000 to 2015. Individual comorbidities were prospectively collected at the time of ASCT. The impact of HCT-CI and other potential prognostic factors, including Karnofsky performance score (KPS), on NRM and survival were studied in multivariate Cox regression models. Results: HCT-CI score was 0, 1, 2, 3, and >3 in 42%, 18%, 13%, 13%, and 14% of the study cohort, respectively. Subjects were stratified into 3 risk groups: HCT-CI score of 0 (42%) versus HCT-CI score of 1 to 2 (32%) versus HCT-CI score > 2 (26%). Higher HCT-CI was associated with lower KPS < 90 (33% of subject’s score of 0 versus 50% in HCT-CI score > 2). HCT-CI score > 2 was associated with melphalan dose reduction (22% versus 10% in score 0 cohorts). One-year NRM was low at 2% (95% confidence interval, 1% to 4%). On multivariate analysis, overall survival was inferior in groups with HCT-CI score of 1 to 2 (relative risk, 1.37, [95% confidence interval, 1.01 to 1.87], P = .04) and HCT-CI score > 2 (relative risk, 1.5 [95% confidence interval, 1.09 to 2.08], P = .01). Factors that affect OS in the autologous recipients among lymphoma and myeloma patients were: HCT-CI, Karnofsky score, number of CD34+ cells/kg and time from diagnosis until transplant (p<0.05). Factors that affect TRM/NRM were HCT-CI, ECOG, Karnofsky score and number of hospital days and body weight.(p<0.05). Conclusions: ASCT for MM and lymphoma is associated with low NRM, and death is predominantly related to disease progression. Comorbidity evaluation during autologous transplantation for lymphoproliferative diseases can be a useful tool in predicting transplant outcome. </jats:p>en_US
dc.language.isoenen_US
dc.publisherAmerican Society of Clinical Oncology (ASCO)en_US
dc.relation.ispartofJournal of Clinical Oncologyen_US
dc.titleOutcome after autologous transplantation in the terms of comorbidity for patients with lymphoproliferative diseases: Single center experienceen_US
dc.typeProceeding articleen_US
dc.identifier.doi10.1200/jco.2017.35.15_suppl.e19502-
dc.identifier.urlhttp://ascopubs.org/doi/pdfdirect/10.1200/JCO.2017.35.15_suppl.e19502-
dc.identifier.volume35-
dc.identifier.issue15_suppl-
dc.identifier.fpagee19502-
dc.identifier.lpagee19502-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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