Complications of Autologous Stem Cell Transplantation in Multiple Myeloma: Results from the CALM Study

  • Anna Waszczuk-Gajda
  • Olaf Penack
  • Giulia Sbianchi
  • Linda Koster
  • Didier Blaise
  • Péter Reményi
  • Nigel Russell
  • Per Ljungman
  • Marek Trneny
  • Jiri Mayer
  • Simona Iacobelli
  • Guido Kobbe
  • Christof Scheid
  • Jane Apperley
  • Cyrille Touzeau
  • Stig Lenhoff
  • Esa Jantunen
  • Achilles Anagnostopoulos
  • Laura Paris
  • Paul Browne
  • Catherine Thieblemont
  • Nicolaas Schaap
  • Jorge Sierra
  • Ibrahim Yakoub-Agha
  • Laurent Garderet
  • Jan Styczynski
  • Helene Schoemans
  • Ivan Moiseev
  • Rafael F Duarte
  • Zinaida Peric
  • Silvia Montoto
  • Anja van Biezen
  • Malgorzata Mikulska
  • Mahmoud Aljurf
  • Tapani Ruutu
  • Nicolaus Kröger
  • Curly Morris
  • Christian Koenecke
  • Stefan Schoenland
  • Grzegorz W Basak

Abstract

Background: The main goal of this post hoc analysis of the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study was to evaluate the rate of short- and long-term infectious and non-infectious complications occurring after ASCT in patients with multiple myeloma (MM). Methods: The analysis included all patients with MM from the CALM study who underwent ≥1 ASCT. The primary endpoint of the analysis was to determine the rate of infectious and non-infectious complications after ASCT and to compare them in three time periods: 0−100 days, 101 days−1 year, and >1 year after the first transplant. Results: The analysis included a total of 3552 patients followed up for a median of 56.7 months (range 0.4−108.1). Complication rates decreased with the time from ASCT with 24.85 cases per 100 patient-years from day 0 to 100 days after the transplant, and <2.31 cases per 100 patient-years from the 101st day. At 100 days after ASC T, 45.7% of patients had complications, with infectious events being twice as frequent as non-infectious complications. Bacterial infections (6.5 cases per 100 patient-years, 95% CI: 6.1−7.0) and gastrointestinal complications (4.7 cases per 100 patient-years, 95% CI: 4.3−5.1) were the most common early events. The pattern of complications changed with time from ASCT. The presence of complications after ASCT was not associated with overall survival. Conclusions: Our data provide a solid basis for comparing ASCT-related complications to those caused by emerging treatments in multiple myeloma, such as CAR T-cell therapy and other immunotherapies.

Bibliografische Daten

OriginalspracheEnglisch
Aufsatznummer3541
ISSN2077-0383
DOIs
StatusVeröffentlicht - 20.06.2022
PubMed 35743620