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Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma
OBJECTIVES: Chimeric antigen receptor T cells (CARTs) against CD19 antigen represent an effective therapy for relapsed/refractory diffuse large B‐cell lymphoma (rrDLBCL). There is no diagnostic test able to predict which patients with residual disease will relapse from those that will reach a delaye...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176123/ https://www.ncbi.nlm.nih.gov/pubmed/35846093 http://dx.doi.org/10.1002/jha2.131 |
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author | Maluquer, Clara Bellosillo, Beatriz Mussetti, Alberto Domingo‐Domènech, Eva Parody, Rocío Fernández‐Ibarrondo, Lierni Velasco, Roser Moreno‐González, Gabriel Sanz, Gabriela Cortés, Montserrat Sureda, Anna |
author_facet | Maluquer, Clara Bellosillo, Beatriz Mussetti, Alberto Domingo‐Domènech, Eva Parody, Rocío Fernández‐Ibarrondo, Lierni Velasco, Roser Moreno‐González, Gabriel Sanz, Gabriela Cortés, Montserrat Sureda, Anna |
author_sort | Maluquer, Clara |
collection | PubMed |
description | OBJECTIVES: Chimeric antigen receptor T cells (CARTs) against CD19 antigen represent an effective therapy for relapsed/refractory diffuse large B‐cell lymphoma (rrDLBCL). There is no diagnostic test able to predict which patients with residual disease will relapse from those that will reach a delayed complete response. Positron emission tomography/computed tomography scan (PET‐CT) is characterized by a significant number of false positive results after immunotherapy. Circulating tumor DNA (ctDNA) may be a good‐useful tool to quantify minimal residual disease and for monitoring disease response. METHODS: We present a patient with DLBCL treated with CART cells in which we tested the combined use of ctDNA and PET‐CT scan. RESULTS: Disease reassessment with PET‐CT scan showed a partial remission (3 weeks) and a very good partial remission (2 months). A clinical progression at 3 months was confirmed with PET‐CT scan. Levels of ctDNA progressively decreased and became undetectable. An initial increase in KMT2D p.E4385G variant allele frequency confirmed disease progression. CONCLUSIONS: Our case shows how the complementary use of ctDNA and PET‐CT scan could be a helpful tool in the clinical management of these patients. |
format | Online Article Text |
id | pubmed-9176123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91761232022-07-14 Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma Maluquer, Clara Bellosillo, Beatriz Mussetti, Alberto Domingo‐Domènech, Eva Parody, Rocío Fernández‐Ibarrondo, Lierni Velasco, Roser Moreno‐González, Gabriel Sanz, Gabriela Cortés, Montserrat Sureda, Anna EJHaem Short Reports OBJECTIVES: Chimeric antigen receptor T cells (CARTs) against CD19 antigen represent an effective therapy for relapsed/refractory diffuse large B‐cell lymphoma (rrDLBCL). There is no diagnostic test able to predict which patients with residual disease will relapse from those that will reach a delayed complete response. Positron emission tomography/computed tomography scan (PET‐CT) is characterized by a significant number of false positive results after immunotherapy. Circulating tumor DNA (ctDNA) may be a good‐useful tool to quantify minimal residual disease and for monitoring disease response. METHODS: We present a patient with DLBCL treated with CART cells in which we tested the combined use of ctDNA and PET‐CT scan. RESULTS: Disease reassessment with PET‐CT scan showed a partial remission (3 weeks) and a very good partial remission (2 months). A clinical progression at 3 months was confirmed with PET‐CT scan. Levels of ctDNA progressively decreased and became undetectable. An initial increase in KMT2D p.E4385G variant allele frequency confirmed disease progression. CONCLUSIONS: Our case shows how the complementary use of ctDNA and PET‐CT scan could be a helpful tool in the clinical management of these patients. John Wiley and Sons Inc. 2020-12-09 /pmc/articles/PMC9176123/ /pubmed/35846093 http://dx.doi.org/10.1002/jha2.131 Text en © 2020 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Reports Maluquer, Clara Bellosillo, Beatriz Mussetti, Alberto Domingo‐Domènech, Eva Parody, Rocío Fernández‐Ibarrondo, Lierni Velasco, Roser Moreno‐González, Gabriel Sanz, Gabriela Cortés, Montserrat Sureda, Anna Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title | Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title_full | Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title_fullStr | Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title_full_unstemmed | Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title_short | Liquid biopsy for disease monitoring after anti‐CD19 chimeric antigen receptor T cell in diffuse large B‐cell lymphoma |
title_sort | liquid biopsy for disease monitoring after anti‐cd19 chimeric antigen receptor t cell in diffuse large b‐cell lymphoma |
topic | Short Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176123/ https://www.ncbi.nlm.nih.gov/pubmed/35846093 http://dx.doi.org/10.1002/jha2.131 |
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