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Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy
PURPOSE: Chimeric antigen receptor (CAR)-T cells are a viable treatment option for patients with relapsed or refractory (r/r) aggressive B-cell lymphomas. The prognosis of patients who relapse after CAR-T cell treatment is dismal and factors predicting outcomes need to be identified. Our aim was to...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356653/ https://www.ncbi.nlm.nih.gov/pubmed/36662305 http://dx.doi.org/10.1007/s00432-023-04587-4 |
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author | Georgi, Thomas Walter Kurch, Lars Franke, Georg-Nikolaus Jentzsch, Madlen Schwind, Sebastian Perez-Fernandez, Carmen Petermann, Naima Merz, Maximilian Metzeler, Klaus Borte, Gudrun Hoffmann, Sandra Herling, Marco Denecke, Timm Kluge, Regine Sabri, Osama Platzbecker, Uwe Vučinić, Vladan |
author_facet | Georgi, Thomas Walter Kurch, Lars Franke, Georg-Nikolaus Jentzsch, Madlen Schwind, Sebastian Perez-Fernandez, Carmen Petermann, Naima Merz, Maximilian Metzeler, Klaus Borte, Gudrun Hoffmann, Sandra Herling, Marco Denecke, Timm Kluge, Regine Sabri, Osama Platzbecker, Uwe Vučinić, Vladan |
author_sort | Georgi, Thomas Walter |
collection | PubMed |
description | PURPOSE: Chimeric antigen receptor (CAR)-T cells are a viable treatment option for patients with relapsed or refractory (r/r) aggressive B-cell lymphomas. The prognosis of patients who relapse after CAR-T cell treatment is dismal and factors predicting outcomes need to be identified. Our aim was to assess the value of FDG-PET/CT in terms of predicting patient outcomes. METHODS: Twenty-two patients with r/r B-cell lymphoma who received CAR-T cell treatment with tisagenlecleucel (n = 17) or axicabtagene ciloleucel (n = 5) underwent quantitative FDG-PET/CT before (PET-0) and 1 month after infusion of CAR-T cells (PET-1). PET-1 was classified as complete metabolic response (CMR, Deauville score 1–3) or non-CMR (Deauville score 4–5). RESULTS: At the time of PET-1, 12/22 (55%) patients showed CMR, ten (45%) patients non-CMR. 7/12 (58%) CMR patients relapsed after a median of 223 days, three of them (25%) died. 9/10 (90%) non-CMR patients developed relapse or progressive disease after a median of 91 days, eight of them (80%) died. CMR patients demonstrated a significantly lower median total metabolic tumor volume (TMTV) in PET-0 (1 ml) than non-CMR patients (225 ml). CONCLUSION: Our results confirm the prognostic value of PET-1. 42% of all CMR patients are still in remission 1 year after CAR T-cell treatment. 90% of the non-CMR patients relapsed, indicating the need for early intervention. Higher TMTV before CAR-T cell infusion was associated with lower chances of CMR. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-023-04587-4. |
format | Online Article Text |
id | pubmed-10356653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103566532023-07-21 Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy Georgi, Thomas Walter Kurch, Lars Franke, Georg-Nikolaus Jentzsch, Madlen Schwind, Sebastian Perez-Fernandez, Carmen Petermann, Naima Merz, Maximilian Metzeler, Klaus Borte, Gudrun Hoffmann, Sandra Herling, Marco Denecke, Timm Kluge, Regine Sabri, Osama Platzbecker, Uwe Vučinić, Vladan J Cancer Res Clin Oncol Research PURPOSE: Chimeric antigen receptor (CAR)-T cells are a viable treatment option for patients with relapsed or refractory (r/r) aggressive B-cell lymphomas. The prognosis of patients who relapse after CAR-T cell treatment is dismal and factors predicting outcomes need to be identified. Our aim was to assess the value of FDG-PET/CT in terms of predicting patient outcomes. METHODS: Twenty-two patients with r/r B-cell lymphoma who received CAR-T cell treatment with tisagenlecleucel (n = 17) or axicabtagene ciloleucel (n = 5) underwent quantitative FDG-PET/CT before (PET-0) and 1 month after infusion of CAR-T cells (PET-1). PET-1 was classified as complete metabolic response (CMR, Deauville score 1–3) or non-CMR (Deauville score 4–5). RESULTS: At the time of PET-1, 12/22 (55%) patients showed CMR, ten (45%) patients non-CMR. 7/12 (58%) CMR patients relapsed after a median of 223 days, three of them (25%) died. 9/10 (90%) non-CMR patients developed relapse or progressive disease after a median of 91 days, eight of them (80%) died. CMR patients demonstrated a significantly lower median total metabolic tumor volume (TMTV) in PET-0 (1 ml) than non-CMR patients (225 ml). CONCLUSION: Our results confirm the prognostic value of PET-1. 42% of all CMR patients are still in remission 1 year after CAR T-cell treatment. 90% of the non-CMR patients relapsed, indicating the need for early intervention. Higher TMTV before CAR-T cell infusion was associated with lower chances of CMR. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-023-04587-4. Springer Berlin Heidelberg 2023-01-20 2023 /pmc/articles/PMC10356653/ /pubmed/36662305 http://dx.doi.org/10.1007/s00432-023-04587-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Georgi, Thomas Walter Kurch, Lars Franke, Georg-Nikolaus Jentzsch, Madlen Schwind, Sebastian Perez-Fernandez, Carmen Petermann, Naima Merz, Maximilian Metzeler, Klaus Borte, Gudrun Hoffmann, Sandra Herling, Marco Denecke, Timm Kluge, Regine Sabri, Osama Platzbecker, Uwe Vučinić, Vladan Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title | Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title_full | Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title_fullStr | Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title_full_unstemmed | Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title_short | Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy |
title_sort | prognostic value of baseline and early response fdg-pet/ct in patients with refractory and relapsed aggressive b-cell lymphoma undergoing car-t cell therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356653/ https://www.ncbi.nlm.nih.gov/pubmed/36662305 http://dx.doi.org/10.1007/s00432-023-04587-4 |
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