Volume 43, Issue S3 e337_70094
SUPPLEMENT ABSTRACTS
Free Access

337 | ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA: AN ANALYSIS FROM THE EBMT LYMPHOMA WORKING PARTY

I. Age Kos

I. Age Kos

Hematology, Oncology and Hematology, University of Saarland, Internal Medicine I, Homburg, Germany

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M. Fekom

M. Fekom

European Society for Blood and Marrow Transplantation, Paris, France

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A. Ossami Saidy

A. Ossami Saidy

Department of Hematology, Oncology and Tumor Immunology, Helios Klinik Berlin-Buch, Berlin, Germany

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R. Duléry

R. Duléry

Hôpital Saint-Antoine, Assistance Publique – Hôpitaux de Paris (AP-HP), Paris, France, Department of Clinical Hematology and Cellular Therapy, Sorbonne University, Paris, France

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C. Thieblemont

C. Thieblemont

Assistance Publique & Hôpitaux de Paris (APHP), Hôpital Saint-Louis, Université de Paris, Hémato-oncologie, Paris, France

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K. Christofyllakis

K. Christofyllakis

Hematology, Oncology and Hematology, University of Saarland, Internal Medicine I, Homburg, Germany

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S. Lenhoff

S. Lenhoff

Skanes University HHospital, Lund, Sweden

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A. Sanchez-Salinas

A. Sanchez-Salinas

Hospital Universitario Virgen de la Arrixaca, Murcia, Spain

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N. Kröger

N. Kröger

University Hospital Eppendorf, Hamburg, Germany

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R. Schroers

R. Schroers

ZSIS Universitaetsklinikum Knappschaftskrankenhaus Bochum GmbH, Bochum, Germany

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G. Illerhaus

G. Illerhaus

Klinikum Stuttgart, Stuttgart, Germany

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O. Hermine

O. Hermine

Hopital Necker Adults, Paris, France

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H. Sengeloev

H. Sengeloev

Rigshospitalet, Herlev, Denmark

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B. Wahlin

B. Wahlin

Karolinska University Hospital, Stockholm, Sweden

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E. Angelucci

E. Angelucci

IRCCS Ospedale Policlinico San Martino, Genova, Italy

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A. Laurence

A. Laurence

University College London Hospital, London, UK

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M. Itäla-Remes

M. Itäla-Remes

Turku University Hospital, Turku, Finland

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P. Chevallier

P. Chevallier

CHU Nantes, Nantes, France

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A. Peniket

A. Peniket

Oxford Radcliffe, Oxford, UK

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L. Bacon

L. Bacon

Department of Haematology, St James's Hospital, Dublin, Ireland

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G. Kobbe

G. Kobbe

Heinrich Heine Universitaet, Duesseldorf, Germany

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A. U. Ural

A. U. Ural

Ankara Bayindir Hospital, Ankara, Turkey

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P. Dreger

P. Dreger

University of Heidelberg, Heidelberg, Germany

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M. J. Pascual Cascon

M. J. Pascual Cascon

Hospital Regional de Málaga, Málaga, Spain

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T. Mika

T. Mika

ZSIS Universitaetsklinikum Knappschaftskrankenhaus Bochum GmbH, Bochum, Germany

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E. Tholouli

E. Tholouli

Manchester Royal Infirmary, Manchester, UK

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A. De Becker

A. De Becker

Universitair Ziekenhuis Brussel, Brussels, Belgium

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M. T. Rubio

M. T. Rubio

CHRU Nancy, Vandoeuvre les Nancy, France

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F. Baron

F. Baron

University of Liege, Liege, Belgium

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L. López Corral

L. López Corral

Hospital Clínico, Salamanca, Spain

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A. Nagler

A. Nagler

Chaim Sheba Medical Center, Tel-Hashomer, Israel

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M. Bornhäuser

M. Bornhäuser

Universitaetsklinikum Dresden, Dresden, Germany

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R. Zeiser

R. Zeiser

University Hospital of Freiburg, Freiburg, Germany

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D. Pastore

D. Pastore

Perrino Hospital, Brindisi, Italy

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L. Gabellier

L. Gabellier

Service d’Hématologie Clinique, CHU de Montpellier, Montpellier, France

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O. G. Sevindik

O. G. Sevindik

Demiroglu Bilim University Istanbul Florence Nightingale Hospital, Instanbul, Turkey

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B. Glass

B. Glass

Department of Hematology, Oncology and Tumor Immunology, Helios Klinik Berlin-Buch, Berlin, Germany

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L. Thurner

L. Thurner

Hematology, Oncology and Hematology, University of Saarland, Internal Medicine I, Homburg, Germany

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A. Bazarbachi

A. Bazarbachi

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

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First published: 16 June 2025

Introduction: Despite a high proportion of patients with primary central nervous system lymphoma (PCNSL) achieving complete remission (CR) following first-line treatment, relapses still occur in about 50% of patients. The prognosis in the relapsed/refractory (R/R) setting remains poor, and therapeutic options, including salvage chemotherapies, radiotherapy, CAR-T-cell or experimental combinations of small molecules like BTKi and IMIDs are limited and partly not approved. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has shown curative potential in various lymphoma subtypes; however, data on its efficacy in PCNSL is limited to a small number of published cases worldwide.

Methods: We conducted a retrospective, registry-based analysis using data from the European Society for Blood and Marrow Transplantation (EBMT), including adult patients diagnosed with PCNSL who underwent allo-HSCT between 2016 and 2022.

Results: A total of 31 patients were included, with a median age of 50 years (range: 22–68) at the time of allo-HSCT. The median follow-up period was 1.5 years (95% CI: 0.9–5.8). Males comprised 58% of the cohort, and 61% of patients had a Karnofsky performance status ≥ 90%. The median time from diagnosis to allo-HSCT was 22 months (range: 4–196). Most patients were heavily pretreated, with 54% having received ≥ 3 prior lines of therapy, 12% having received two, and 35% having received one. Prior to allo-HSCT, 57% of patients were in CR, 23% in partial remission (PR), and 20% had active R/R disease. The most frequently used conditioning regimen was a combination of Busulfan, Fludarabine, and Thiotepa (42%). Post-transplant cyclophosphamide was administered in 40% of patients. Total body irradiation (TBI) based conditioning was used in 23% of cases. Donors were predominantly related (48% matched, 26% haploidentical), while 26% were unrelated. The overall survival (OS) rates at 1 and 2 years were 34.9%. Progression-free survival (PFS) at 1 and 2 years was 30.8%. The relapse incidence (RI) was 39.6% in the first year and did not increase in the second year. Non-relapse mortality was 29.7% at 1 and 2 years. Chronic graft-versus-host disease was observed in 24.9% of patients at both 1 and 2 years. The GvHD-free, relapse-free survival (GRFS) rates were 19.9% at 1 and 2 years.

Conclusion: In this large registry-based cohort of patients with PCNSL undergoing allo-HSCT, our findings indicate that allo-HSCT is an effective treatment in a subset of patients. The stable RI beyond one year may suggest a potential for long-term disease control in approximately one third of transplanted patients.

Research funding declaration: This is an analysis supported by the EBMT Lymphoma Working Party

Keywords: cellular therapies; aggressive B-cell non-Hodgkin lymphoma; extranodal non-Hodgkin lymphoma

No potential sources of conflict of interest.

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