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


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 01 2019
Historique:
received: 06 06 2018
revised: 26 07 2018
accepted: 13 08 2018
pubmed: 24 10 2018
medline: 12 10 2019
entrez: 24 10 2018
Statut: ppublish

Résumé

The treatment of patients with Hodgkin lymphoma (HL) who develop disease progression after undergoing allogeneic stem cell transplantation (allo-SCT) remains challenging. 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. 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<.001), approximately 34% of the original BV cohort were alive and in CR at the time of last follow-up versus 18% in the group that did not receive BV (P=.003). The use of BV before donor lymphocyte infusion was found to be associated with the highest probability of being alive and in CR (40%) at the time of last follow-up. Salvage BV appeared to have no effect on chronic graft-versus-host disease or 1-year overall survival from the time of disease recurrence after allo-SCT (76% vs 67%). BV is a safe and effective salvage therapy for patients with HL who develop disease recurrence or progression after undergoing allo-SCT, even after prior exposure to BV.

Sections du résumé

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<.001), approximately 34% of the original BV cohort were alive and in CR at the time of last follow-up versus 18% in the group that did not receive BV (P=.003). The use of BV before donor lymphocyte infusion was found to be associated with the highest probability of being alive and in CR (40%) at the time of last follow-up. Salvage BV appeared to have no effect on chronic graft-versus-host disease or 1-year overall survival from the time of disease recurrence after allo-SCT (76% vs 67%).
CONCLUSIONS
BV is a safe and effective salvage therapy for patients with HL who develop disease recurrence or progression after undergoing allo-SCT, even after prior exposure to BV.

Identifiants

pubmed: 30351488
doi: 10.1002/cncr.31755
doi:

Substances chimiques

Immunoconjugates 0
Brentuximab Vedotin 7XL5ISS668

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-98

Informations de copyright

© 2018 American Cancer Society.

Auteurs

Ali Bazarbachi (A)

Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.

Ariane Boumendil (A)

European Society for Blood and Marrow Transplantation Lymphoma Working Party Paris Office, Saint-Antoine Hospital, Paris, France.

Hervé Finel (H)

European Society for Blood and Marrow Transplantation Lymphoma Working Party Paris Office, Saint-Antoine Hospital, Paris, France.

Mohamad Mohty (M)

Department of Hematology and Cell Therapy, Saint Antoine Hospital, Sorbonne University, Paris, France.

Luca Castagna (L)

Department of Hematology and Oncology, Humanitas Clinic Institute, Rozzano Milan, Italy.

Didier Blaise (D)

Department of Hematology, Paoli Calmettes Institute, Marseille, France.

Karl S Peggs (KS)

Department of Hematology, University College London Hospital, London, United Kingdom.

Boris Afanasyev (B)

Department of Hematology, First State Pavlov Medical University of St. Petersburg, St. Petersburg, Russia.

J L Diez-Martin (JL)

Department of Hematology, Gregorio Maranon Hospital, Madrid, Spain.

Paolo Corradini (P)

Department of Hematology, IRCCS National Cancer Institute, University of Milan, Milan, Italy.

David Michonneau (D)

Department of Hematology and Stem Cell Transplant, St. Louis Hospital, Paris, France.

Stephen Robinson (S)

Department of Hematology and Oncology, University Hospital Bristol, Bristol, United Kingdom.

Gonzalo Gutiérrez García (G)

Department of Hematology and Oncology, Hospital Clinic, Barcelona, Spain.

Francesca Bonifazi (F)

Department of Hematology and Medical Oncology, Hematology Department "Seragnoli," S. Orsola-Malpighi University Hospital, Bologna, Italy.

Ibrahim Yakoub-Agha (I)

Department of Hematology, Lille Regional Hospital Center, LIRIC INSERM U995, Lille University, Lille, France.

Zafer Gülbas (Z)

Department of Hematologic Oncology and Bone Marrow Transplantation, Anadolu Medical Center Hospital, Kocaeli, Turkey.

Adrian Bloor (A)

Department of Hematology and Stem Cell Transplant, Christie NHS Foundation Trust, Manchester, United Kingdom.

Jeremy Delage (J)

Department of Clinical Hematology, Lapeyronie Regional Hospital Center, Montpellier, France.

Albert Esquirol (A)

Department of Hematology, Santa Creu i Sant Pau Hospital, Barcelona, Spain.

Ram Malladi (R)

Department of Hematology, Queen Elizabeth Hospital, Birmingham, United Kingdom.

Christof Scheid (C)

Department of Internal Medicine, University of Cologne, Cologne, Germany.

Jean El-Cheikh (J)

Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.

Hervé Ghesquières (H)

Department of Hematology, South Lyon Medical Center, Lyon, France.

Silvia Montoto (S)

Department of Haemato-oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.

Peter Dreger (P)

Department of Medicine V, University of Heidelberg, Heidelberg, Germany.

Anna Sureda (A)

Department of Haematology, Catala Oncology Institute, Barcelona, Spain.

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