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

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Waszczuk-Gajda, A. | Penack, O. | Sbianchi, G. | Koster, L. | Blaise, Didier | Reményi, P. | Russell, N. | Ljungman, P. | Trneny, M. | Mayer, J. | Iacobelli, S. | Kobbe, G. | Scheid, C. | Apperley, J. | Touzeau, Cyrille | Lenhoff, S. | Jantunen, E. | Anagnostopoulos, A. | Paris, L. | Browne, P. | Thieblemont, Catherine | Schaap, N. | Sierra, J. | Yakoub-Agha, Ibrahim | Garderet, Laurent | Styczynski, J. | Schoemans, H. | Moiseev, I. | Duarte, R. F. | Peric, Z. | Montoto, S. | van Biezen, A. | Mikulska, M. | Aljurf, M. | Ruutu, T. | Kröger, N. | Morris, C. | Koenecke, C. | Schoenland, S. | Basak, G. W.

Edité par CCSD ; MDPI -

International audience. 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.

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