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Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy
In AL amyloidosis complete response (aCR) is defined as negative serum and urine immunofixation with normalized free light chain ratio (FLCR). However, achievement of low levels of involved FLC (iFLC) or difference between iFLC and uninvolved FLC (dFLC) are also relevant endpoints for treatment. We...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463008/ https://www.ncbi.nlm.nih.gov/pubmed/32873771 http://dx.doi.org/10.1038/s41408-020-00355-6 |
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author | Milani, Paolo Basset, Marco Nuvolone, Mario Benigna, Francesca Rodigari, Lara Lavatelli, Francesca Foli, Andrea Merlini, Giampaolo Palladini, Giovanni |
author_facet | Milani, Paolo Basset, Marco Nuvolone, Mario Benigna, Francesca Rodigari, Lara Lavatelli, Francesca Foli, Andrea Merlini, Giampaolo Palladini, Giovanni |
author_sort | Milani, Paolo |
collection | PubMed |
description | In AL amyloidosis complete response (aCR) is defined as negative serum and urine immunofixation with normalized free light chain ratio (FLCR). However, achievement of low levels of involved FLC (iFLC) or difference between iFLC and uninvolved FLC (dFLC) are also relevant endpoints for treatment. We divided 434 consecutive patients with AL amyloidosis into five groups according to response 6 months after treatment initiation: aCR, iFLC <20 mg/L, normalized-iFLC, dFLC <10 mg/L, and normalized FLC ratio. Overall survival (OS) was similar (median not reached) in patients in aCR and in those who reached iFLC <20 mg/L, while it was inferior in all other groups (medians ranging from 79 to 91 months). Time to next therapy or death (TNTD) was longer in subjects attaining aCR (median 69 months) than in subjects reaching any FLC endpoint (medians ranging from 18 to 39 months). The ability of discriminating patients who survived more than 2 years among all responders was greater for current definition of aCR compared to combination of negative serum and urine immunofixation with any low-FLC endpoint. Complete response predicts best outcomes in AL amyloidosis and should be the goal of therapy if tolerability allows. |
format | Online Article Text |
id | pubmed-7463008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74630082020-09-11 Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy Milani, Paolo Basset, Marco Nuvolone, Mario Benigna, Francesca Rodigari, Lara Lavatelli, Francesca Foli, Andrea Merlini, Giampaolo Palladini, Giovanni Blood Cancer J Article In AL amyloidosis complete response (aCR) is defined as negative serum and urine immunofixation with normalized free light chain ratio (FLCR). However, achievement of low levels of involved FLC (iFLC) or difference between iFLC and uninvolved FLC (dFLC) are also relevant endpoints for treatment. We divided 434 consecutive patients with AL amyloidosis into five groups according to response 6 months after treatment initiation: aCR, iFLC <20 mg/L, normalized-iFLC, dFLC <10 mg/L, and normalized FLC ratio. Overall survival (OS) was similar (median not reached) in patients in aCR and in those who reached iFLC <20 mg/L, while it was inferior in all other groups (medians ranging from 79 to 91 months). Time to next therapy or death (TNTD) was longer in subjects attaining aCR (median 69 months) than in subjects reaching any FLC endpoint (medians ranging from 18 to 39 months). The ability of discriminating patients who survived more than 2 years among all responders was greater for current definition of aCR compared to combination of negative serum and urine immunofixation with any low-FLC endpoint. Complete response predicts best outcomes in AL amyloidosis and should be the goal of therapy if tolerability allows. Nature Publishing Group UK 2020-09-01 /pmc/articles/PMC7463008/ /pubmed/32873771 http://dx.doi.org/10.1038/s41408-020-00355-6 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Milani, Paolo Basset, Marco Nuvolone, Mario Benigna, Francesca Rodigari, Lara Lavatelli, Francesca Foli, Andrea Merlini, Giampaolo Palladini, Giovanni Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title | Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title_full | Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title_fullStr | Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title_full_unstemmed | Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title_short | Indicators of profound hematologic response in AL amyloidosis: complete response remains the goal of therapy |
title_sort | indicators of profound hematologic response in al amyloidosis: complete response remains the goal of therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463008/ https://www.ncbi.nlm.nih.gov/pubmed/32873771 http://dx.doi.org/10.1038/s41408-020-00355-6 |
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