Impact of rituximab on treatment outcomes of patients with angioimmunoblastic T-cell lymphoma; a population-based analysis.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
11 2022
Historique:
received: 17 06 2022
revised: 08 09 2022
accepted: 08 09 2022
pubmed: 9 10 2022
medline: 22 11 2022
entrez: 8 10 2022
Statut: ppublish

Résumé

Patients with angioimmunoblastic T-cell lymphoma (AITL) are treated with cyclophosphamide, doxorubicin, vincristine and prednisone with or without etoposide (CHO(E)P). In the majority of cases, Epstein-Barr virus (EBV)-positive B-cells are present in the tumour. There is paucity of research examining the effect of rituximab when added to CHO(E)P. In this nationwide, population-based study, we analysed the impact of rituximab on overall response rate (ORR), progression-free survival (PFS) and overall survival (OS) of patients with AITL. Patients with AITL diagnosed between 2014 and 2020 treated with ≥one cycle of CHO(E)P with or without rituximab were identified in the Netherlands Cancer Registry. Survival follow-up was up to 1st February 2022. Baseline characteristics, best response during first-line treatment and survival were collected. PFS was defined as the time from diagnosis to relapse or to all-cause-death. OS was defined as the time from diagnosis to all-cause-death. Multivariable analysis for the risk of mortality was performed using Cox regression. Out of 335 patients, 146 patients (44%) received R-CHO(E)P. Rituximab was more frequently used in patients with a B-cell infiltrate (71% versus 89%, p < 0·01). The proportion of patients who received autologous stem cell transplantation (ASCT) was similar between CHO(E)P and R-CHO(E)P (27% versus 30%, respectively). The ORR and 2-year PFS for patients who received CHO(E)P and R-CHO(E)P were 71% and 78% (p = 0·01), and 40% and 45% (p = 0·12), respectively. The 5-year OS was 47% and 40% (p = 0·99), respectively. In multivariable analysis, IPI-score 3-5, no B-cell infiltrate and no ASCT were independent prognostic factors for risk of mortality, whereas the use of rituximab was not. Although the addition of rituximab to CHO(E)P improved ORR for patients with AITL, the PFS and OS did not improve.

Sections du résumé

BACKGROUND
Patients with angioimmunoblastic T-cell lymphoma (AITL) are treated with cyclophosphamide, doxorubicin, vincristine and prednisone with or without etoposide (CHO(E)P). In the majority of cases, Epstein-Barr virus (EBV)-positive B-cells are present in the tumour. There is paucity of research examining the effect of rituximab when added to CHO(E)P. In this nationwide, population-based study, we analysed the impact of rituximab on overall response rate (ORR), progression-free survival (PFS) and overall survival (OS) of patients with AITL.
METHODS
Patients with AITL diagnosed between 2014 and 2020 treated with ≥one cycle of CHO(E)P with or without rituximab were identified in the Netherlands Cancer Registry. Survival follow-up was up to 1st February 2022. Baseline characteristics, best response during first-line treatment and survival were collected. PFS was defined as the time from diagnosis to relapse or to all-cause-death. OS was defined as the time from diagnosis to all-cause-death. Multivariable analysis for the risk of mortality was performed using Cox regression.
FINDINGS
Out of 335 patients, 146 patients (44%) received R-CHO(E)P. Rituximab was more frequently used in patients with a B-cell infiltrate (71% versus 89%, p < 0·01). The proportion of patients who received autologous stem cell transplantation (ASCT) was similar between CHO(E)P and R-CHO(E)P (27% versus 30%, respectively). The ORR and 2-year PFS for patients who received CHO(E)P and R-CHO(E)P were 71% and 78% (p = 0·01), and 40% and 45% (p = 0·12), respectively. The 5-year OS was 47% and 40% (p = 0·99), respectively. In multivariable analysis, IPI-score 3-5, no B-cell infiltrate and no ASCT were independent prognostic factors for risk of mortality, whereas the use of rituximab was not.
INTERPRETATION
Although the addition of rituximab to CHO(E)P improved ORR for patients with AITL, the PFS and OS did not improve.

Identifiants

pubmed: 36208568
pii: S0959-8049(22)00743-2
doi: 10.1016/j.ejca.2022.09.008
pii:
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Antibodies, Monoclonal, Murine-Derived 0
Vincristine 5J49Q6B70F
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT
Doxorubicin 80168379AG

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100-109

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Frederik O Meeuwes (FO)

Department of Hematology, Treant Hospital, Emmen, the Netherlands; Department of Hematology, University Medical Center Groningen, Groningen, the Netherlands.

Mirian Brink (M)

Department of Research and Development, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, the Netherlands.

Marjolein W M van der Poel (MWM)

Department of Internal Medicine, Division of Hematology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, the Netherlands.

Marie José Kersten (MJ)

Department of Hematology, Amsterdam University Medical Centers, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, the Netherlands.

Mariëlle Wondergem (M)

Department of Hematology, Amsterdam University Medical Centers, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, the Netherlands.

Pim G N J Mutsaers (PGNJ)

Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.

Lara Böhmer (L)

Department of Hematology, Haga Hospital, The Hague, the Netherlands.

Sherida Woei-A-Jin (S)

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

Otto Visser (O)

Department of Hematology, Isala Hospital, Zwolle, the Netherlands.

Rimke Oostvogels (R)

Department of Hematology, University Medical Center Utrecht, Utrecht, the Netherlands.

Patty M Jansen (PM)

Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.

Arjan Diepstra (A)

Department of Pathology, University Medical Center Groningen, Groningen, the Netherlands.

Tjeerd J F Snijders (TJF)

Department of Hematology, Medisch Spectrum Twente, Enschede, the Netherlands.

Wouter J Plattel (WJ)

Department of Hematology, University Medical Center Groningen, Groningen, the Netherlands.

Gerwin A Huls (GA)

Department of Hematology, University Medical Center Groningen, Groningen, the Netherlands.

Joost S P Vermaat (JSP)

Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.

Marcel Nijland (M)

Department of Hematology, University Medical Center Groningen, Groningen, the Netherlands. Electronic address: m.nijland@umcg.nl.

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Classifications MeSH