Ute Hegenbart
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Autologous stem cell transplantation for AL amyloidosis: a multicenter summary of outcomes 2010–2020
Abstract The role of autologous stem cell transplantation (ASCT) is central in AL amyloidosis and continues to be defined in the era of newer therapies. To evaluate contemporary patient selection, practice patterns, and outcomes, we conducted a retrospective, multicenter study across nine tertiary referral centers, including 1047 patients with AL amyloidosis who underwent ASCT between 2010 and 2020.
Determinants of Long-Term Benefit From High Dose Melphalan With Autologous Stem Cell Transplant in AL Amyloidosis
Filename Description ajh70371-sup-0001-Supinfo.docxWord 2007 document , 313.8 KB Table S1: Baseline characteristics of non-landmarked population. Table S2: Cox regression analyses for predictors of EFS. Table S3: Cox regression analysis for EFS stratified by receipt of HDM a there were 90 events in the no HDM cohort, and 84 events in the HDM cohort. Figure S1: Flowchart of cohort selection. Figure S2: Overall survival and time to progression before and after 12-month landmark analysis.
Blood phosphorylated tau elevation as a biomarker in immunoglobulin light chain and transthyretin amyloidosis
Abstract Elevated blood levels of phosphorylated tau (p-tau) are diagnostic of Alzheimer disease and are associated with the deposition of amyloid-β in the cerebral neuropil. Elevated p-tau levels have also been associated with cerebral deposition of Danish amyloid and prion protein amyloid. Here we analyzed p-tau in serum from four different cohorts of people with the most common types of systemic amyloidosis, transthyretin (ATTR) amyloidosis and immunoglobulin light chain (AL) amyloidosis.
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