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Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma

Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma (MM) is lacking in the current literature. We evaluated 258 patients with relapsed MM, diagnosed from 2008 to 2015, to investigate the prognostic impact of deep immunoparesis on post‐relapse survival. On qualitative...

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Autores principales: Chakraborty, Rajshekhar, Rybicki, Lisa, Nakashima, Megan O., Dean, Robert M., Faiman, Beth M., Samaras, Christy J., Rosko, Nathaniel, Dysert, Hayley, Valent, Jason, Anwer, Faiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292652/
https://www.ncbi.nlm.nih.gov/pubmed/32108328
http://dx.doi.org/10.1111/bjh.16488
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author Chakraborty, Rajshekhar
Rybicki, Lisa
Nakashima, Megan O.
Dean, Robert M.
Faiman, Beth M.
Samaras, Christy J.
Rosko, Nathaniel
Dysert, Hayley
Valent, Jason
Anwer, Faiz
author_facet Chakraborty, Rajshekhar
Rybicki, Lisa
Nakashima, Megan O.
Dean, Robert M.
Faiman, Beth M.
Samaras, Christy J.
Rosko, Nathaniel
Dysert, Hayley
Valent, Jason
Anwer, Faiz
author_sort Chakraborty, Rajshekhar
collection PubMed
description Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma (MM) is lacking in the current literature. We evaluated 258 patients with relapsed MM, diagnosed from 2008 to 2015, to investigate the prognostic impact of deep immunoparesis on post‐relapse survival. On qualitative immunoparesis assessment, no, partial and full immunoparesis was present in 9%, 30% and 61% of patients, respectively. Quantitative immunoparesis was assessed by computing the average relative difference (ARD) between polyclonal immunoglobulin(s) and corresponding lower normal limit(s), with greater negative values indicating deeper immunoparesis. The median ARD was −39%, with an optimal cut‐off of −50% for overall survival (OS) by recursive partitioning analysis. Deep immunoparesis (ARD ≤–50%) was associated with a higher tumour burden at first relapse compared to none/shallow [ARD >−50%] immunoparesis. The OS (P = 0·007) and progression‐free survival (PFS; P < 0·001) differed significantly between the deep and none/shallow immunoparesis groups. Kaplan–Meier estimates for 3‐year OS were 36% and 46%, and for 2‐year PFS were 17% and 27%, respectively. On multivariable analysis (MVA) for PFS, both qualitative and quantitative immunoparesis retained negative prognostic impact independently. However, only quantitative immunoparesis was independently prognostic for OS on MVA. Depth of immunoparesis in relapsed MM is an important prognostic factor for post‐relapse survival in the era of novel agents and continuous therapy.
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spelling pubmed-92926522022-07-20 Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma Chakraborty, Rajshekhar Rybicki, Lisa Nakashima, Megan O. Dean, Robert M. Faiman, Beth M. Samaras, Christy J. Rosko, Nathaniel Dysert, Hayley Valent, Jason Anwer, Faiz Br J Haematol Haematological Malignancy ‐ Clinical Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma (MM) is lacking in the current literature. We evaluated 258 patients with relapsed MM, diagnosed from 2008 to 2015, to investigate the prognostic impact of deep immunoparesis on post‐relapse survival. On qualitative immunoparesis assessment, no, partial and full immunoparesis was present in 9%, 30% and 61% of patients, respectively. Quantitative immunoparesis was assessed by computing the average relative difference (ARD) between polyclonal immunoglobulin(s) and corresponding lower normal limit(s), with greater negative values indicating deeper immunoparesis. The median ARD was −39%, with an optimal cut‐off of −50% for overall survival (OS) by recursive partitioning analysis. Deep immunoparesis (ARD ≤–50%) was associated with a higher tumour burden at first relapse compared to none/shallow [ARD >−50%] immunoparesis. The OS (P = 0·007) and progression‐free survival (PFS; P < 0·001) differed significantly between the deep and none/shallow immunoparesis groups. Kaplan–Meier estimates for 3‐year OS were 36% and 46%, and for 2‐year PFS were 17% and 27%, respectively. On multivariable analysis (MVA) for PFS, both qualitative and quantitative immunoparesis retained negative prognostic impact independently. However, only quantitative immunoparesis was independently prognostic for OS on MVA. Depth of immunoparesis in relapsed MM is an important prognostic factor for post‐relapse survival in the era of novel agents and continuous therapy. John Wiley and Sons Inc. 2020-02-28 2020-06 /pmc/articles/PMC9292652/ /pubmed/32108328 http://dx.doi.org/10.1111/bjh.16488 Text en © 2020 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Haematological Malignancy ‐ Clinical
Chakraborty, Rajshekhar
Rybicki, Lisa
Nakashima, Megan O.
Dean, Robert M.
Faiman, Beth M.
Samaras, Christy J.
Rosko, Nathaniel
Dysert, Hayley
Valent, Jason
Anwer, Faiz
Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title_full Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title_fullStr Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title_full_unstemmed Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title_short Characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
title_sort characterisation and prognostic impact of immunoparesis in relapsed multiple myeloma
topic Haematological Malignancy ‐ Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292652/
https://www.ncbi.nlm.nih.gov/pubmed/32108328
http://dx.doi.org/10.1111/bjh.16488
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