Incidence of Second Primary Malignancies after Autologous Transplantation for Multiple Myeloma in the Era of Novel Agents

The advent of novel agents for multiple myeloma (MM) is cause for a re-examination of the incidence of second primary malignancies (SPM5). We examined the SPM rate in MM patients who were enrolled in the prospective observational CALM (Collaboration to Collect Autologous Transplant outcome in Lymphoma and Myeloma) study. Between 2008 and 2012, 3204 patients with MM underwent a first autologous hematopoietic stem cell transplantation. Plerixafor was used as a mobilizing agent for patients with poor (or potentially poor) stem cell mobilization as defined by the respective centers. A total of 135... Mehr ...

Verfasser: Didier Blaise
Soledad González Muñiz
Jane F. Apperley
Nicolaus Kröger
Péter Reményi
Nicolaas Schaap
Firoozeh Sahebi
Stig Lenhoff
Ibrahim Yakoub-Agha
Marta Krejčí
Nigel H. Russell
Giulia Sbianchi
Marek Trneny
Guido Kobbe
Wieslaw Wiktor-Jedrzejczak
Cecilia Isaksson
Christof Scheid
Stefan Schönland
Laurent Garderet
Curly Morris
Per Ljungman
Paul Browne
Linda Koster
Simona Iacobelli
James F. Sanchez
Keith Wilson
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Schlagwörter: Netherlands / Knowmad Institut / Transplantation / Hematology
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26811681
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://www.openaccessrepository.it/record/83071

The advent of novel agents for multiple myeloma (MM) is cause for a re-examination of the incidence of second primary malignancies (SPM5). We examined the SPM rate in MM patients who were enrolled in the prospective observational CALM (Collaboration to Collect Autologous Transplant outcome in Lymphoma and Myeloma) study. Between 2008 and 2012, 3204 patients with MM underwent a first autologous hematopoietic stem cell transplantation. Plerixafor was used as a mobilizing agent for patients with poor (or potentially poor) stem cell mobilization as defined by the respective centers. A total of 135 patients developed SPM5, with a cumulative incidence of 5.3% (95% confidence interval, 4.4 to 6.3) at 72 months. Ninety-four patients developed solid tumors, 30 developed hematologic malignancies, and 11 developed an SPM of an unknown type. The cumulative incidence of known hematologic and solid malignancies were 1.4% and 3.6%, respectively, at 72 months. In a univariate analysis, use of radiotherapy, type of induction regimen, hematopoietic stem cell dose, poor mobilizer status, plerixafor use, and sex did not influence the cumulative incidence of SPMs. Only age over 65 years was statistically associated with an increased incidence. Overall, the incidence of SPMs was comparable to earlier estimations of SPMs in MM. (C) 2018 American Society for Blood and Marrow Transplantation.