Brentuximab vedotin is associated with improved progression-free survival after allogeneic transplantation for Hodgkin lymphoma

Biol Blood Marrow Transplant. 2014 Nov;20(11):1864-8. doi: 10.1016/j.bbmt.2014.06.037. Epub 2014 Jul 5.

Abstract

We previously reported that brentuximab vedotin (BV) enabled successful reduced-intensity allogeneic hematopoietic cell transplantation (RIC-alloHCT) in patients with relapsed Hodgkin lymphoma, after a median follow-up of 14.4 months. We now provide an updated report on 21 patients who were treated from 2009 to 2012 with BV before RIC-alloHCT with a uniform fludarabine/melphalan conditioning regimen and donor source after a median follow-up of 29.9 months. We have also retrospectively compared the patient characteristics and outcomes of these BV-pretreated patients to 23 patients who received fludarabine/melphalan RIC-alloHCT without prior BV, in the time period before the drug was available (2003 to 2009). Patients who were treated with BV before RIC-alloHCT had a lower median hematopoietic cell transplantation-specific comorbidity index and a reduced number of peri-transplantation toxicities. There were also improvements in 2-year progression-free survival (59.3% versus 26.1%) and cumulative incidence of relapse/progression (23.8% versus 56.5%).

Keywords: Allogeneic transplantation; Brentuximab vedotin; Hodgkin lymphoma; Reduced-intensity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brentuximab Vedotin
  • Disease-Free Survival
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Hodgkin Disease / drug therapy
  • Hodgkin Disease / therapy*
  • Humans
  • Immunoconjugates / therapeutic use*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Transplantation Conditioning
  • Young Adult

Substances

  • Immunoconjugates
  • Brentuximab Vedotin