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Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma

This manuscript reviews current advances in the use of radioimmunotherapy (RIT) for the treatment of B-cell non-Hodgkin’s lymphoma (NHL). RIT has been in use for more than 20 years and has progressed significantly with the discovery of new molecular targets, the development of new stable chelates, t...

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Autores principales: Bodet-Milin, Caroline, Ferrer, Ludovic, Pallardy, Amandine, Eugène, Thomas, Rauscher, Aurore, Alain Faivre-Chauvet, Barbet, Jacques, Kraeber-Bodéré, Françoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708100/
https://www.ncbi.nlm.nih.gov/pubmed/23875170
http://dx.doi.org/10.3389/fonc.2013.00177
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author Bodet-Milin, Caroline
Ferrer, Ludovic
Pallardy, Amandine
Eugène, Thomas
Rauscher, Aurore
Alain Faivre-Chauvet,
Barbet, Jacques
Kraeber-Bodéré, Françoise
author_facet Bodet-Milin, Caroline
Ferrer, Ludovic
Pallardy, Amandine
Eugène, Thomas
Rauscher, Aurore
Alain Faivre-Chauvet,
Barbet, Jacques
Kraeber-Bodéré, Françoise
author_sort Bodet-Milin, Caroline
collection PubMed
description This manuscript reviews current advances in the use of radioimmunotherapy (RIT) for the treatment of B-cell non-Hodgkin’s lymphoma (NHL). RIT has been in use for more than 20 years and has progressed significantly with the discovery of new molecular targets, the development of new stable chelates, the humanization of monoclonal antibodies (MAbs), and the use of pretargeting techniques. Today, two products targeting the CD20 antigen are approved: (131)I-tositumomab (Bexxar(®)), and (90)Y-ibritumomab tiuxetan (Zevalin(®)). (131)I-tositumomab is available in the United States, and (90)Y-ibritumumab tiuxetan in Europe, the United States, Asia, and Africa. RIT can be integrated in clinical practice using non-ablative activities for treatment of patients with relapsed or refractory follicular lymphoma (FL) or as consolidation after induction chemotherapy in front-line treatment in FL patients. Despite the lack of phase III studies to clearly define the efficacy of RIT in the management of B lymphoma in the era of rituximab-based therapy, RIT efficacy in NHL has been demonstrated. In relapsing refractory FL and transformed NHL, RIT as a monotherapy induces around 30% complete response with a possibility of durable remissions. RIT consolidation after induction therapy significantly improves the quality of the response. Dose-limiting toxicity of RIT is hematological, depending on bone marrow involvement and prior treatment. Non-hematological toxicity is generally low. Different studies have been published assessing innovative protocols of RIT or new indications, in particular treatment in patients with aggressive lymphomas. High-dose treatment, RIT as consolidation after different therapeutic induction modalities, RIT in first-line treatment or fractionated RIT showed promising results. New MAbs, in particular humanized MAbs, or combinations of naked and radiolabeled MAbs, also appear promising. Personalized dosimetry protocols should be developed to determine injected activity.
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spelling pubmed-37081002013-07-19 Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma Bodet-Milin, Caroline Ferrer, Ludovic Pallardy, Amandine Eugène, Thomas Rauscher, Aurore Alain Faivre-Chauvet, Barbet, Jacques Kraeber-Bodéré, Françoise Front Oncol Oncology This manuscript reviews current advances in the use of radioimmunotherapy (RIT) for the treatment of B-cell non-Hodgkin’s lymphoma (NHL). RIT has been in use for more than 20 years and has progressed significantly with the discovery of new molecular targets, the development of new stable chelates, the humanization of monoclonal antibodies (MAbs), and the use of pretargeting techniques. Today, two products targeting the CD20 antigen are approved: (131)I-tositumomab (Bexxar(®)), and (90)Y-ibritumomab tiuxetan (Zevalin(®)). (131)I-tositumomab is available in the United States, and (90)Y-ibritumumab tiuxetan in Europe, the United States, Asia, and Africa. RIT can be integrated in clinical practice using non-ablative activities for treatment of patients with relapsed or refractory follicular lymphoma (FL) or as consolidation after induction chemotherapy in front-line treatment in FL patients. Despite the lack of phase III studies to clearly define the efficacy of RIT in the management of B lymphoma in the era of rituximab-based therapy, RIT efficacy in NHL has been demonstrated. In relapsing refractory FL and transformed NHL, RIT as a monotherapy induces around 30% complete response with a possibility of durable remissions. RIT consolidation after induction therapy significantly improves the quality of the response. Dose-limiting toxicity of RIT is hematological, depending on bone marrow involvement and prior treatment. Non-hematological toxicity is generally low. Different studies have been published assessing innovative protocols of RIT or new indications, in particular treatment in patients with aggressive lymphomas. High-dose treatment, RIT as consolidation after different therapeutic induction modalities, RIT in first-line treatment or fractionated RIT showed promising results. New MAbs, in particular humanized MAbs, or combinations of naked and radiolabeled MAbs, also appear promising. Personalized dosimetry protocols should be developed to determine injected activity. Frontiers Media S.A. 2013-07-11 /pmc/articles/PMC3708100/ /pubmed/23875170 http://dx.doi.org/10.3389/fonc.2013.00177 Text en Copyright © 2013 Bodet-Milin, Ferrer, Pallardy, Eugène, Rauscher, Faivre-Chauvet, Barbet and Kraeber-Bodéré. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Oncology
Bodet-Milin, Caroline
Ferrer, Ludovic
Pallardy, Amandine
Eugène, Thomas
Rauscher, Aurore
Alain Faivre-Chauvet,
Barbet, Jacques
Kraeber-Bodéré, Françoise
Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title_full Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title_fullStr Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title_full_unstemmed Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title_short Radioimmunotherapy of B-Cell Non-Hodgkin’s Lymphoma
title_sort radioimmunotherapy of b-cell non-hodgkin’s lymphoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708100/
https://www.ncbi.nlm.nih.gov/pubmed/23875170
http://dx.doi.org/10.3389/fonc.2013.00177
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