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Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network

Adoptive cellular therapy using chimeric antigen receptor T-cell (CART) therapy is currently being evaluated in patients with relapsed / refractory multiple myeloma (MM). The majority of CAR-T cell programs now being tested in clinical trials are targeting B-cell maturation antigen. Several recent p...

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Autores principales: Moreau, Philippe, Sonneveld, Pieter, Boccadoro, Mario, Cook, Gordon, Mateos, Ma Victoria, Nahi, Hareth, Goldschmidt, Hartmut, Dimopoulos, Meletios A., Lucio, Paulo, Bladé, Joan, Delforge, Michel, Hajek, Roman, Ludwig, Heinz, Facon, Thierry, Miguel, Jesus F. San, Einsele, Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959167/
https://www.ncbi.nlm.nih.gov/pubmed/31439675
http://dx.doi.org/10.3324/haematol.2019.224204
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author Moreau, Philippe
Sonneveld, Pieter
Boccadoro, Mario
Cook, Gordon
Mateos, Ma Victoria
Nahi, Hareth
Goldschmidt, Hartmut
Dimopoulos, Meletios A.
Lucio, Paulo
Bladé, Joan
Delforge, Michel
Hajek, Roman
Ludwig, Heinz
Facon, Thierry
Miguel, Jesus F. San
Einsele, Hermann
author_facet Moreau, Philippe
Sonneveld, Pieter
Boccadoro, Mario
Cook, Gordon
Mateos, Ma Victoria
Nahi, Hareth
Goldschmidt, Hartmut
Dimopoulos, Meletios A.
Lucio, Paulo
Bladé, Joan
Delforge, Michel
Hajek, Roman
Ludwig, Heinz
Facon, Thierry
Miguel, Jesus F. San
Einsele, Hermann
author_sort Moreau, Philippe
collection PubMed
description Adoptive cellular therapy using chimeric antigen receptor T-cell (CART) therapy is currently being evaluated in patients with relapsed / refractory multiple myeloma (MM). The majority of CAR-T cell programs now being tested in clinical trials are targeting B-cell maturation antigen. Several recent phase I / II trials show promising preliminary results in patients with MM progressing on proteasome inhibitors, immunomodulatory drugs and monoclonal antibodies targeting CD38. CAR-T cell therapy is a potentially life-threatening strategy that can only be administered in experienced centers. For the moment, CAR-T cell therapy for MM is still experimental, but once this strategy has been approved in relapsed/refractory MM, it will become one of the most important indications for this therapy in Europe and world-wide. This manuscript proposes practical considerations for the use of CAR-T cell therapy in MM, and discusses several important issues for its future development.
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spelling pubmed-69591672020-01-22 Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network Moreau, Philippe Sonneveld, Pieter Boccadoro, Mario Cook, Gordon Mateos, Ma Victoria Nahi, Hareth Goldschmidt, Hartmut Dimopoulos, Meletios A. Lucio, Paulo Bladé, Joan Delforge, Michel Hajek, Roman Ludwig, Heinz Facon, Thierry Miguel, Jesus F. San Einsele, Hermann Haematologica Guideline Article Adoptive cellular therapy using chimeric antigen receptor T-cell (CART) therapy is currently being evaluated in patients with relapsed / refractory multiple myeloma (MM). The majority of CAR-T cell programs now being tested in clinical trials are targeting B-cell maturation antigen. Several recent phase I / II trials show promising preliminary results in patients with MM progressing on proteasome inhibitors, immunomodulatory drugs and monoclonal antibodies targeting CD38. CAR-T cell therapy is a potentially life-threatening strategy that can only be administered in experienced centers. For the moment, CAR-T cell therapy for MM is still experimental, but once this strategy has been approved in relapsed/refractory MM, it will become one of the most important indications for this therapy in Europe and world-wide. This manuscript proposes practical considerations for the use of CAR-T cell therapy in MM, and discusses several important issues for its future development. Ferrata Storti Foundation 2019-12 /pmc/articles/PMC6959167/ /pubmed/31439675 http://dx.doi.org/10.3324/haematol.2019.224204 Text en Copyright© 2019 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Guideline Article
Moreau, Philippe
Sonneveld, Pieter
Boccadoro, Mario
Cook, Gordon
Mateos, Ma Victoria
Nahi, Hareth
Goldschmidt, Hartmut
Dimopoulos, Meletios A.
Lucio, Paulo
Bladé, Joan
Delforge, Michel
Hajek, Roman
Ludwig, Heinz
Facon, Thierry
Miguel, Jesus F. San
Einsele, Hermann
Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title_full Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title_fullStr Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title_full_unstemmed Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title_short Chimeric antigen receptor T-cell therapy for multiple myeloma: a consensus statement from The European Myeloma Network
title_sort chimeric antigen receptor t-cell therapy for multiple myeloma: a consensus statement from the european myeloma network
topic Guideline Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959167/
https://www.ncbi.nlm.nih.gov/pubmed/31439675
http://dx.doi.org/10.3324/haematol.2019.224204
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