Autologous Stem Cell Transplantation in Multiple Myeloma in the Era of Novel Drug Induction: A Retrospective Single-Center Analysis

  • Gabriela B Thoennissen
  • Dennis Görlich
  • Ulrike Bacher
  • Thomas Aufenberg
  • Anne-Christin Hüsken
  • Anna Antonia Hansmeier
  • Georg Evers
  • Jan-Henrik Mikesch
  • Fleur Fritz
  • Carsten Bokemeyer
  • Carsten Müller-Tidow
  • Matthias Stelljes
  • Rolf M Mesters
  • Utz Krug
  • Martin H Kropff
  • Nils H Thoennissen
  • Wolfgang E Berdel

Related Research units

Abstract

Within this retrospective single-center study, we analyzed the survival of 320 multiple myeloma (MM) patients receiving melphalan high-dose chemotherapy (HDCT) and either single (n = 286) or tandem (n = 34) autologous stem cell transplantation (ASCT) from 1996 to 2012. Additionally, the impact of novel induction regimens was assessed. Median follow-up was 67 months, median overall survival (OS) 62 months, median progression-free survival (PFS) 33 months (95% CI 27-39), and treatment-related death (TRD) 3%. Multivariate analysis revealed age ≥60 years (p = 0.03) and stage 3 according to the International Staging System (p = 0.006) as adverse risk factors regarding PFS. Median OS was significantly better in newly diagnosed MM patients receiving induction therapy with novel agents, e.g., bortezomib, thalidomide, or lenalidomide, compared with a traditional regimen (69 vs. 58 months; p = 0.01). More patients achieved at least a very good partial remission in the period from 2005 to 2012 than from 1996 to 2004 (65 vs. 30%; p < 0.001), with a longer median OS in the later period (71 vs. 52 months, p = 0.027). In conclusion, our analysis confirms HDCT-ASCT as an effective therapeutic strategy in an unselected large myeloma patient cohort with a low TRD rate and improved prognosis due to novel induction strategies.

Bibliographical data

Original languageEnglish
ISSN0001-5792
DOIs
Publication statusPublished - 2017
PubMed 28399522