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The median age at HCT was 35 years (range, 18.1\u201068.6 years), and the median length of follow\u2010up was 7.1 years after HCT (range, 1\u201024.3 years).<\/jats:p><\/jats:sec><jats:sec><jats:title>RESULTS.<\/jats:title><jats:p>Sixty patients with CKD were identified, resulting in a cumulative incidence of 4.4% at 5 years (autologous HCT, 3.8%; matched\u2010sibling HCT, 4.5%; unrelated donor HCT, 10%; <jats:italic>P<\/jats:italic> = .09 compared with autologous HCT). Older age at HCT (relative risk [RR] per 5\u2010year increment, 1.33; 95% confidence interval [CI], 1.2\u20101.5), exposure to cyclosporine without tacrolimus (RR, 1.90; 95% CI, 1.1\u20103.4) or with tacrolimus (RR, 4.59; 95% CI, 1.8\u201011.5), and a primary diagnosis of multiple myeloma (RR, 2.51; 95% CI, 1.1\u20105.6) were associated with an increased risk of delayed CKD.<\/jats:p><\/jats:sec><jats:sec><jats:title>CONCLUSIONS.<\/jats:title><jats:p>In this study, the authors identified a subpopulation of patients who underwent HCT and remained at increased risk for CKD. The current findings set the stage for appropriate long\u2010term follow\u2010up of vulnerable patients. Cancer 2008. \u00a9 2008 American Cancer Society.<\/jats:p><\/jats:sec>","DOI":"10.1002\/cncr.23773","type":"journal-article","created":{"date-parts":[[2008,8,14]],"date-time":"2008-08-14T18:08:23Z","timestamp":1218737303000},"page":"1580-1587","source":"Crossref","is-referenced-by-count":69,"title":["Incidence and predictors of delayed chronic kidney disease in long\u2010term survivors of hematopoietic cell 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