Prognostication of survival using cardiac troponins and N-terminal pro-brain natriuretic peptide in patients with primary systemic amyloidosis undergoing peripheral blood stem cell transplantation
Author:
Dispenzieri Angela1, Gertz Morie A.1, Kyle Robert A.1, Lacy Martha Q.1, Burritt Mary F.1, Therneau Terry M.1, McConnell Joseph P.1, Litzow Mark R.1, Gastineau Dennis A.1, Tefferi Ayalew1, Inwards David J.1, Micallef Ivana N.1, Ansell Stephen M.1, Porrata Luis F.1, Elliott Michelle A.1, Hogan William J.1, Rajkumar S. Vincent1, Fonseca Rafael1, Greipp Philip R.1, Witzig Thomas E.1, Lust John A.1, Zeldenrust Steven R.1, Snow Denise S.1, Hayman Susan R.1, McGregor Christopher G. A.1, Jaffe Allan S.1
Affiliation:
1. From the Division of Hematology and Internal Medicine, the Division of Biostatistics, the Division of Cardiovascular Diseases and Internal Medicine, the Division of Laboratory Genetics, the Department of Surgery, and the Division of Clinical Biochemistry and Immunology, Mayo Clinic, Rochester, MN.
Abstract
Abstract
Primary systemic amyloidosis (AL) is a fatal plasma cell disorder. Pilot data suggest survival is better in patients undergoing peripheral blood stem cell transplantation (PBSCT), but the selection process makes the apparent benefit suspect. We have reported that circulating cardiac biomarkers are the best predictors of survival outside of the transplantation setting. We now test whether cardiac troponins (cTnT and cTnI) and N-terminal pro-brain natriuretic peptide (NT-proBNP) are prognostic in transplant recipients. In 98 patients with AL undergoing PBSCT, serum cardiac biomarkers were measured (cTnT, 98 patients; cTnI, 65 patients; and NT-proBNP, 63 patients). Elevated levels of cTnT, cTnI, and NT-proBNP were present in 14%, 43%, and 48% of patients, respectively. At 20 months median follow-up, median survival has not been reached for patients with values below the thresholds; in patients with values above the thresholds, median survival is 26.1 months, 66.1 months, and 66.1 months, respectively. Our previously reported risk systems incorporating these markers were also prognostic, notably the cTnT/NT-proBNP staging. Using this system, 49%, 38%, and 13% of patients were in stage I, stage II, and stage III, respectively. Determining levels of circulating biomarkers may be the most powerful tool for staging patients with AL undergoing PBSCT.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Reference40 articles.
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