Long-term survival outcomes of reduced-intensity allogeneic or autologous transplantation in relapsed grade 3 follicular lymphoma

  • Evgeny Klyuchnikov
  • U Bacher
  • K Woo Ahn
  • J Carreras
  • Nicolaus-Martin Kröger
  • P N Hari
  • G H Ku
  • E Ayala
  • A I Chen
  • Y-B Chen
  • J B Cohen
  • C O Freytes
  • R P Gale
  • R T Kamble
  • M A Kharfan-Dabaja
  • H M Lazarus
  • R Martino
  • A Mussetti
  • B N Savani
  • H C Schouten
  • S Z Usmani
  • P H Wiernik
  • B Wirk
  • S M Smith
  • A Sureda
  • M Hamadani

Abstract

Grade 3 follicular lymphoma (FL) has aggressive clinical behavior. To evaluate the optimal first transplantation approach in relapsed/refractory grade 3 FL patients, we compared the long-term outcomes after allogeneic (allo-) vs autologous hematopoietic cell transplantation (auto-HCT) in the rituximab era. A total of 197 patients undergoing first reduced-intensity conditioning (RIC) allo-HCT or first auto-HCT during 2000-2012 were included. Rituximab-naive patients were excluded. Allo-HCT recipients were younger, more heavily pretreated and had a longer interval between diagnosis and HCT. The 5-year probabilities of non-relapse mortality (NRM), relapse/progression, PFS and overall survival (OS) for auto-HCT vs allo-HCT groups were 4% vs 27% (P<0.001), 61% vs 20% (P<0.001), 36% vs 51% (P=0.07) and 59% vs 54% (P=0.7), respectively. On multivariate analysis, auto-HCT was associated with reduced risk of NRM (relative risk (RR)=0.20; P=0.001). Within the first 11 months post HCT, auto- and allo-HCT had similar risks of relapse/progression and PFS. Beyond 11 months, auto-HCT was associated with higher risk of relapse/progression (RR=21.3; P=0.003) and inferior PFS (RR=3.2; P=0.005). In the first 24 months post HCT, auto-HCT was associated with improved OS (RR=0.42; P=0.005), but in long-time survivors (beyond 24 months) it was associated with inferior OS (RR=3.6; P=0.04). RIC allo-HCT as the first transplant approach can provide improved PFS and OS, in long-term survivors.Bone Marrow Transplantation advance online publication, 5 October 2015; doi:10.1038/bmt.2015.223.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0268-3369
DOIs
StatusVeröffentlicht - 05.10.2015
PubMed 26437062