Back to Search Start Over

Brentuximab vedotin for recurrent Hodgkin lymphoma after allogeneic hematopoietic stem cell transplantation: A report from the EBMT Lymphoma Working Party

Authors :
Adrian Bloor
Stephen D. Robinson
Peter Dreger
Ram Malladi
Gonzalo Gutierrez Garcia
Silvia Montoto
Albert Esquirol
Hervé Ghesquières
Didier Blaise
Zafer Gulbas
Boris V. Afanasyev
Herve Finel
Karl S. Peggs
Mohamad Mohty
Ariane Boumendil
David Michonneau
Francesca Bonifazi
Jean El-Cheikh
Jeremy Delage
Ibrahim Yakoub-Agha
Anna Sureda
Christof Scheid
Ali Bazarbachi
Paolo Corradini
Luca Castagna
J. L. Diez-Martin
Source :
Cancer. 125:90-98
Publication Year :
2018
Publisher :
Wiley, 2018.

Abstract

BACKGROUND: The treatment of patients with Hodgkin lymphoma (HL) who develop disease progression after undergoing allogeneic stem cell transplantation (allo‐SCT) remains challenging. METHODS: The authors assessed outcomes in 184 adult patients with HL who developed disease recurrence or progression after a matched related or unrelated allo‐SCT at European Society for Blood and Marrow Transplantation–participating centers between 2010 and 2014. RESULTS: Eighty patients who received brentuximab vedotin (BV) salvage therapy were compared with 104 patients who did not. Patients in the BV group were younger (median age of 30 years vs 34 years) and were more likely to receive pretransplant BV (65% vs 46%) or posttransplant donor lymphocyte infusion (66% vs 33%). The 2 groups otherwise were comparable. Patients in the BV group received a median of 6 doses of posttransplant BV, resulting in a complete remission rate of 29%, a partial response rate of 45%, and a stable disease rate of 26%. Response to BV after allo‐SCT did not appear to be affected by receipt of pretransplant BV. Despite a longer median follow‐up for surviving patients in the BV group (33 months vs 23 months; P

Details

ISSN :
0008543X
Volume :
125
Database :
OpenAIRE
Journal :
Cancer
Accession number :
edsair.doi...........e568285f12ff805cdf808734fafc6b23
Full Text :
https://doi.org/10.1002/cncr.31755