Bortezomib-based induction followed by stem cell transplantation in light chain amyloidosis: results of the multicenter HOVON 104 trial

  • Monique C Minnema
  • Kazem Nasserinejad
  • Bouke Hazenberg
  • Ute Hegenbart
  • Philip Vlummens
  • Paula F Ypma
  • Nicolaus Kröger
  • Ka Lung Wu
  • Marie Jose Kersten
  • M Ron Schaafsma
  • Sandra Croockewit
  • Esther de Waal
  • Sonja Zweegman
  • Lidwien Tick
  • Annemieke Broijl
  • Harry Koene
  • Gerard Bos
  • Pieter Sonneveld
  • Stefan Schönland

Abstract

This prospective, multicenter, phase II study investigated the use of four cycles of bortezomib-dexamethasone induction treatment, followed by high-dose melphalan and autologous stem cell transplantation (SCT) in patients with newly diagnosed light chain amyloidosis. The aim of the study was to improve the hematologic complete remission (CR) rate 6 months after SCT from 30% to 50%. Fifty patients were enrolled and 72% had two or more organs involved. The overall hematologic response rate after induction treatment was 80% including 20% CR and 38% very good partial remissions (VGPR). Fifteen patients did not proceed to SCT for various reasons but mostly treatment-related toxicity and disease-related organ damage and death (2 patients). Thirty-one patients received melphalan 200 mg/m2 and four patients a reduced dose because of renal function impairment. There were no deaths related to the transplantation procedure. Hematologic responses improved at 6 months after SCT to 86% with 46% CR and 26% VGPR. However, due to the high treatment discontinuation rate before transplantation the primary endpoint of the study was not met and the CR rate in the intention-to-treat analysis was 32%. Organ responses continued to improve after SCT. We confirm the high efficacy of bortezomib-dexamethasone treatment in patients with AL amyloidosis. However, because of both treatment-related toxicity and disease characteristics, 30% of the patients could not proceed to SCT after induction treatment. (Trial registered at Dutch Trial Register identifier NTR3220).

Bibliographical data

Original languageEnglish
ISSN0390-6078
DOIs
Publication statusPublished - 11.2019
PubMed 30923094