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Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases
Up to 60% of patients with aggressive B-cell lymphoma who receive chimeric antigen receptor (CAR) T-cell therapy experience treatment failure and subsequently have a poor prognosis. Allogeneic hematopoietic stem cell transplantation (alloHSCT) remains a potentially curative approach for patients in...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481921/ https://www.ncbi.nlm.nih.gov/pubmed/34604075 http://dx.doi.org/10.3389/fonc.2021.737645 |
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author | Gerhardt, Kristin Jentzsch, Madlen Georgi, Thomas Sretenović, Aleksandra Cross, Michael Bach, Enrica Monecke, Astrid Leiblein, Sabine Hoffmann, Sandra Todorović, Milena Bila, Jelena Sabri, Osama Schwind, Sebastian Franke, Georg-Nikolaus Platzbecker, Uwe Vučinić, Vladan |
author_facet | Gerhardt, Kristin Jentzsch, Madlen Georgi, Thomas Sretenović, Aleksandra Cross, Michael Bach, Enrica Monecke, Astrid Leiblein, Sabine Hoffmann, Sandra Todorović, Milena Bila, Jelena Sabri, Osama Schwind, Sebastian Franke, Georg-Nikolaus Platzbecker, Uwe Vučinić, Vladan |
author_sort | Gerhardt, Kristin |
collection | PubMed |
description | Up to 60% of patients with aggressive B-cell lymphoma who receive chimeric antigen receptor (CAR) T-cell therapy experience treatment failure and subsequently have a poor prognosis. Allogeneic hematopoietic stem cell transplantation (alloHSCT) remains a potentially curative approach for patients in this situation. Induction of a deep response prior to alloHSCT is crucial for long-term outcomes, but the optimal bridging strategy following relapse after CAR T-cell therapy has not yet been established. Polatuzumab vedotin, an antibody drug conjugate targeting CD79b, is a novel treatment option for use in combination with rituximab and bendamustine (Pola-BR) in relapsed or refractory disease. Patients: We report two heavily pretreated patients with primary refractory diffuse large B-cell lymphoma (DLBCL) and primary mediastinal B-cell lymphoma (PMBCL) respectively who relapsed after therapy with CAR T-cells with both nodal and extranodal manifestations of the disease. After application of three courses of Pola-BR both patients achieved a complete metabolic remission. Both patients underwent alloHSCT from a human leukocyte antigen (HLA)-mismatched donor following conditioning with busulfan and fludarabine and are disease free 362 days and 195 days after alloHSCT respectively. We conclude that Pola-BR can be an effective bridging therapy before alloHSCT of patients relapsing after CAR T-cell therapy. Further studies will be necessary to define the depth and durability of remission of this salvage regimen before alloHSCT. |
format | Online Article Text |
id | pubmed-8481921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84819212021-10-01 Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases Gerhardt, Kristin Jentzsch, Madlen Georgi, Thomas Sretenović, Aleksandra Cross, Michael Bach, Enrica Monecke, Astrid Leiblein, Sabine Hoffmann, Sandra Todorović, Milena Bila, Jelena Sabri, Osama Schwind, Sebastian Franke, Georg-Nikolaus Platzbecker, Uwe Vučinić, Vladan Front Oncol Oncology Up to 60% of patients with aggressive B-cell lymphoma who receive chimeric antigen receptor (CAR) T-cell therapy experience treatment failure and subsequently have a poor prognosis. Allogeneic hematopoietic stem cell transplantation (alloHSCT) remains a potentially curative approach for patients in this situation. Induction of a deep response prior to alloHSCT is crucial for long-term outcomes, but the optimal bridging strategy following relapse after CAR T-cell therapy has not yet been established. Polatuzumab vedotin, an antibody drug conjugate targeting CD79b, is a novel treatment option for use in combination with rituximab and bendamustine (Pola-BR) in relapsed or refractory disease. Patients: We report two heavily pretreated patients with primary refractory diffuse large B-cell lymphoma (DLBCL) and primary mediastinal B-cell lymphoma (PMBCL) respectively who relapsed after therapy with CAR T-cells with both nodal and extranodal manifestations of the disease. After application of three courses of Pola-BR both patients achieved a complete metabolic remission. Both patients underwent alloHSCT from a human leukocyte antigen (HLA)-mismatched donor following conditioning with busulfan and fludarabine and are disease free 362 days and 195 days after alloHSCT respectively. We conclude that Pola-BR can be an effective bridging therapy before alloHSCT of patients relapsing after CAR T-cell therapy. Further studies will be necessary to define the depth and durability of remission of this salvage regimen before alloHSCT. Frontiers Media S.A. 2021-09-16 /pmc/articles/PMC8481921/ /pubmed/34604075 http://dx.doi.org/10.3389/fonc.2021.737645 Text en Copyright © 2021 Gerhardt, Jentzsch, Georgi, Sretenović, Cross, Bach, Monecke, Leiblein, Hoffmann, Todorović, Bila, Sabri, Schwind, Franke, Platzbecker and Vučinić https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Gerhardt, Kristin Jentzsch, Madlen Georgi, Thomas Sretenović, Aleksandra Cross, Michael Bach, Enrica Monecke, Astrid Leiblein, Sabine Hoffmann, Sandra Todorović, Milena Bila, Jelena Sabri, Osama Schwind, Sebastian Franke, Georg-Nikolaus Platzbecker, Uwe Vučinić, Vladan Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title | Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title_full | Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title_fullStr | Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title_full_unstemmed | Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title_short | Salvage Therapy With Polatuzumab Vedotin, Bendamustine, and Rituximab Prior to Allogeneic Hematopoietic Transplantation in Patients With Aggressive Lymphomas Relapsing After Therapy With Chimeric Antigen Receptor T-Cells—Report on Two Cases |
title_sort | salvage therapy with polatuzumab vedotin, bendamustine, and rituximab prior to allogeneic hematopoietic transplantation in patients with aggressive lymphomas relapsing after therapy with chimeric antigen receptor t-cells—report on two cases |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481921/ https://www.ncbi.nlm.nih.gov/pubmed/34604075 http://dx.doi.org/10.3389/fonc.2021.737645 |
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