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Blood, 15 September 2004, Vol. 104, No. 6, pp. 1881-1887.
Prepublished online as a Blood First Edition Paper on March 25, 2004; DOI 10.1182/blood-2004-01-0390.
Previous Article | Next Article 
Submitted February 2, 2004
Accepted March 10, 2004
Prognostication of Survival using Cardiac Troponins and N-terminal pro-Brain Natriuretic Peptide in Patients with Primary Systemic Amyloidosis Undergoing Peripheral Blood Stem Cell Transplant
Angela Dispenzieri*, Morie A Gertz, Robert A Kyle, Martha Q Lacy, Mary F Burritt, Terry M Therneau, Joseph P McConnell, Mark R Litzow, Dennis A Gastineau, Ayalew Tefferi, David J Inwards, Ivana N Micallef, Stephen M Ansell, Luis F Porrata, Michelle A Elliott, William J Hogan, S V Rajkumar, Rafael Fonseca, Philip R Greipp, Thomas E Witzig, John A Lust, Steven R Zeldenrust, Denise S Snow, Susan R Hayman, Christopher G McGregor, and Allan S Jaffe
Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA
Clinical Biochemistry and Immunology, Mayo Clinic, Rochester, MN, USA
Biostatistics, Mayo Clinic, Rochester, MN, USA
Laboratory Genetics, Mayo Clinic, Rochester, MN, USA
Surgery, Mayo Clinic, Rochester, MN, USA
Cardiovascular Diseases and Internal Medicine, Mayo Clinic, Rochester, MN, USA; Laboratory Genetics, Mayo Clinic, Rochester, MN, USA
* Corresponding author; email: dispenzieri.angela{at}mayo.edu.
Primary systemic amyloidosis (AL) is a fatal plasma cell disorder. Pilot data suggest survival is better in patients undergoing peripheral blood stem cell transplant (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 transplant setting. We now test whether cardiac troponins (cTnT and cTnI) and N-terminal pro-brain natriuretic peptide (NT-proBNP) are prognostic in transplant patients. Ninety-eight patients with AL undergoing PBSCT had serum cardiac biomarkers measured (cTnT, 98; cTnI, 65; and NT-proBNP, 63 patients). Elevated levels of cTnT, cTnI, NT-proBNP were present in 14%, 43%, and 48%, respectively. At 20 months median follow-up, median survival has not been reached for patients with values below the thresholds and is 26.1, 66.1 and 66.1 months if above. 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 Stage I, II, and III, respectively, lower stage for stage than a previously reported cohort of patients not undergoing transplant. Levels of circulating biomarkers may be the most powerful tools for staging patients with AL undergoing PBSCT.

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