Refinement in patient selection to reduce treatment-related mortality from autologous stem cell transplantation in amyloidosis

Bone Marrow Transplant. 2013 Apr;48(4):557-61. doi: 10.1038/bmt.2012.170. Epub 2012 Sep 10.

Abstract

This study sought to develop selection guidelines to determine the eligibility for SCT of patients with light-chain amyloidosis. Patients with biopsy-confirmed lightchain amyloidosis who underwent SCT between 8 March 1996 and 31 December 2011 were reviewed in two cohorts by date of transplantation: between 8 March 1996 and 30 June 2009 (n=410) and between 1 July 2009 and 31 December 2011 (n=89). Also evaluated were patients who died before post-transplant day 100 to determine the features predictive of early death. After 1 July 2009, fewer transplant recipients had Mayo stage III cardiac involvement. Mortality before post-transplant day 100 was 10.5% (43/410) in the earlier group and 1.1% (1/89) in the later group. In the earlier group, one-quarter of transplant recipients with N-terminal pro-brain natriuretic peptide (NT-proBNP) >5000 pg/mL died by 10.3 months. When serum troponin T was >0.06 ng/mL, 25% died at 3.7 months. The Mayo staging system is predictive for OS but not useful for selecting transplant recipients. Patients with serum troponin T >0.06 ng/mL or NT-proBNP >5000 pg/mL (not on dialysis) should not be considered candidates for SCT because of early mortality.

Publication types

  • Clinical Trial

MeSH terms

  • Amyloidosis* / blood
  • Amyloidosis* / mortality
  • Amyloidosis* / pathology
  • Amyloidosis* / therapy
  • Disease-Free Survival
  • Female
  • Follow-Up Studies
  • Heart Diseases / blood
  • Heart Diseases / etiology
  • Heart Diseases / mortality
  • Heart Diseases / pathology
  • Humans
  • Male
  • Middle Aged
  • Natriuretic Peptide, Brain / blood*
  • Patient Selection*
  • Retrospective Studies
  • Stem Cell Transplantation*
  • Survival Rate
  • Time Factors
  • Transplantation, Autologous
  • Troponin T / blood*

Substances

  • Troponin T
  • Natriuretic Peptide, Brain