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Isatuximab: A Review of Its Use in Multiple Myeloma
Isatuximab (Sarclisa(®); isatuximab-irfc in the USA) is an anti-CD38 monoclonal antibody (mAb) approved for use in the treatment of adults with multiple myeloma (MM): in combination with pomalidomide and dexamethasone for those with relapsed and refractory MM (RRMM) who have received ≥ 2 prior thera...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497289/ https://www.ncbi.nlm.nih.gov/pubmed/34351561 http://dx.doi.org/10.1007/s11523-021-00827-0 |
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author | Frampton, James E. |
author_facet | Frampton, James E. |
author_sort | Frampton, James E. |
collection | PubMed |
description | Isatuximab (Sarclisa(®); isatuximab-irfc in the USA) is an anti-CD38 monoclonal antibody (mAb) approved for use in the treatment of adults with multiple myeloma (MM): in combination with pomalidomide and dexamethasone for those with relapsed and refractory MM (RRMM) who have received ≥ 2 prior therapies, including lenalidomide and a proteasome inhibitor; and in combination with carfilzomib and dexamethasone for those with relapsed MM who have received ≥ 1 prior therapy. In phase III studies, the addition of isatuximab to pomalidomide and dexamethasone significantly prolonged progression-free survival (PFS) and improved the depth of tumour response in patients with RRMM, as did the addition of isatuximab to carfilzomib and dexamethasone in patients with relapsed or refractory MM. Health-related quality of life was maintained when isatuximab was combined with these other therapies. Isatuximab-based combination therapies were generally well tolerated and demonstrated a manageable safety profile with no new safety signals. Although mature overall survival data are awaited, available evidence indicates that the combinations of isatuximab with pomalidomide and dexamethasone and isatuximab with carfilzomib and dexamethasone are important additional treatment options for RRMM and relapsed MM, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11523-021-00827-0. |
format | Online Article Text |
id | pubmed-8497289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84972892021-10-19 Isatuximab: A Review of Its Use in Multiple Myeloma Frampton, James E. Target Oncol Adis Drug Evaluation Isatuximab (Sarclisa(®); isatuximab-irfc in the USA) is an anti-CD38 monoclonal antibody (mAb) approved for use in the treatment of adults with multiple myeloma (MM): in combination with pomalidomide and dexamethasone for those with relapsed and refractory MM (RRMM) who have received ≥ 2 prior therapies, including lenalidomide and a proteasome inhibitor; and in combination with carfilzomib and dexamethasone for those with relapsed MM who have received ≥ 1 prior therapy. In phase III studies, the addition of isatuximab to pomalidomide and dexamethasone significantly prolonged progression-free survival (PFS) and improved the depth of tumour response in patients with RRMM, as did the addition of isatuximab to carfilzomib and dexamethasone in patients with relapsed or refractory MM. Health-related quality of life was maintained when isatuximab was combined with these other therapies. Isatuximab-based combination therapies were generally well tolerated and demonstrated a manageable safety profile with no new safety signals. Although mature overall survival data are awaited, available evidence indicates that the combinations of isatuximab with pomalidomide and dexamethasone and isatuximab with carfilzomib and dexamethasone are important additional treatment options for RRMM and relapsed MM, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11523-021-00827-0. Springer International Publishing 2021-08-05 2021 /pmc/articles/PMC8497289/ /pubmed/34351561 http://dx.doi.org/10.1007/s11523-021-00827-0 Text en © Springer Nature 2021, corrected publication 2021 https://creativecommons.org/licenses/by-nc/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Adis Drug Evaluation Frampton, James E. Isatuximab: A Review of Its Use in Multiple Myeloma |
title | Isatuximab: A Review of Its Use in Multiple Myeloma |
title_full | Isatuximab: A Review of Its Use in Multiple Myeloma |
title_fullStr | Isatuximab: A Review of Its Use in Multiple Myeloma |
title_full_unstemmed | Isatuximab: A Review of Its Use in Multiple Myeloma |
title_short | Isatuximab: A Review of Its Use in Multiple Myeloma |
title_sort | isatuximab: a review of its use in multiple myeloma |
topic | Adis Drug Evaluation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497289/ https://www.ncbi.nlm.nih.gov/pubmed/34351561 http://dx.doi.org/10.1007/s11523-021-00827-0 |
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