Outcome in patients with diffuse large B-cell lymphoma who relapse after autologous stem cell transplantation and receive active therapy. A retrospective analysis of the Lymphoma Working Party of the European Society for Blood and Marrow Transplantation (EBMT).


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
02 2020
Historique:
received: 27 02 2019
accepted: 09 08 2019
revised: 22 07 2019
pubmed: 22 9 2019
medline: 22 6 2021
entrez: 22 9 2019
Statut: ppublish

Résumé

Autologous hematopoietic stem cell transplantation (auto-HSCT) is the standard of care for patients with diffuse large B-cell lymphoma (DLBCL) who relapse/progress after first line chemoimmunotherapy. Long-term outcome of those who relapse after transplant is poor. We present the results of a retrospective study of 256 adult patients reported to the EBMT registry with DLBCL who relapsed after auto-HSCT performed between 2003 and 2013, and who received active salvage strategies. One hundred and fifty-four (60%) were male; median age was 53 years. Median time to relapse was 7 months, 65% relapsed during the first year. Overall response rate after salvage therapy was 46%. Median follow-up after first salvage therapy was 40 months (IQR 23-63 months). Overall survival (OS) at 3 years was 27% (95% CI 22-33). OS at 3 years of patients relapsing longer than 1 year after auto-HSCT was 41% (95% CI 31-53) compared with 20% (95% CI 14-24) in those who relapsed in less than 1 year. Eighty-two patients (32%) had a second HSCT, an allogeneic HSCT (allo-HSCT) in 69 cases, at a median time of 6.5 months after relapse. OS at 3 years after allo-HSCT was 36% (95% CI 25-51). In conclusion, the prognosis of patients with DLBCL that relapse after auto-HSCT is dismal. Patients who relapse in less than 1 year remain an unmet need, and should be considered for CAR T cell therapy or clinical trials. Patients who relapse after 1 year can be rescued with salvage therapies and a second HSCT. These results provide a benchmark to compare data of new prospective studies.

Identifiants

pubmed: 31541205
doi: 10.1038/s41409-019-0650-x
pii: 10.1038/s41409-019-0650-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

393-399

Références

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Auteurs

E González-Barca (E)

Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain. e.gonzalez@iconcologia.net.

A Boumendil (A)

EBMT Paris Study Office, Paris, France.

D Blaise (D)

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

M Trněný (M)

1st Charles University General Hospital, Prague, Czech Republic.

T Masszi (T)

St. István and St. Laszlo Hospital, Budapest, Hungary.

H Finel (H)

EBMT Paris Study Office, Paris, France.

M G Michieli (MG)

Centro di Riferimento Oncologico, Aviano, Italy.

J T Bittenbring (JT)

University of Saarland, Homburg, Germany.

G Gritti (G)

Papa Giovanni XXIII Hospital, Bergamo, Italy.

J A Snowden (JA)

Sheffield Teaching Hospitals, Sheffield, UK.

M Bishton (M)

Department of Hematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.

B Bruno (B)

Department of Molecular Biotechnology and Health Sciences, AOU Città della Salute e della Scienza, University of Torino, Torino, Italy.

S González de Villambrosia (SG)

Department of Hematology, Hospital Universitario Marqués de Valdecilla, Santander, Spain.

A Janikova (A)

Department of Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.

X Leleu (X)

Service D'Hématologie Et Thérapie Cellulaire, Hopital de La Milétrie, Poitiers, France.

A Anagnostopoulos (A)

Hematology Department & HCT Unit, G. Papanikolaou Hospital, Thessaloniki, Greece.

X Poiré (X)

Section of Hematology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

M Crysandt (M)

Department of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, University Hospital RWTH Aachen University, Aachen, Germany.

Z N Özkurt (ZN)

Gazi University Faculty of Medicine, Ankara, Turkey.

E Vandenberghe (E)

St James Hospital and Trinity College Dublin, Dublin, Ireland.

M Itälä-Remes (M)

Turku University Hospital, Stem Cell Transplantation Unit, Turku, Finland.

J Y Cahn (JY)

Department of Hematology, Hopital A. Michallon, Grenoble, FRA, France.

E Jantunen (E)

University of Eastern Finland/Institute of Clinical Medicine/Internal Medicine, Kuopio, Finland.
Department of Medicine, Kuopio University Hospital, Kuopio, Finland.
Siunsote-North Carelia Hospital District, Joensuu, Finland.

W Schroyens (W)

University of Antwerp, Antwerp University Hospital, Dept. of Hematology, Antwerp, Belgium.

J Maertens (J)

Department of Hematology, University Hospital Gasthuisberg, Dept. of Hematology, Leuven, Belgium.

A Esquirol (A)

Hospital de la Santa Creu i Sant Pau, Clinical Hematology Service, Barcelona, Spain.

P Dreger (P)

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

S Montoto (S)

Haemato-Oncology Department, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

A Sureda (A)

Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain.

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