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Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients

BACKGROUND: Renal impairment (RI) is associated with poor survival in newly diagnosed multiple myeloma (MM) patients. Renal function recovery has been one of the main therapeutic goals in those patients. METHODS: The records from 393 newly diagnosed MM patients in our hospital between January 2012 a...

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Autores principales: Chen, Xuduan, Luo, Xiaofeng, Zu, Yanping, Issa, Hajji Ally, Li, Linlin, Ye, Hong, Yang, Ting, Hu, Jianda, Wei, Lixin
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/PMC7521223/
https://www.ncbi.nlm.nih.gov/pubmed/32710448
http://dx.doi.org/10.1002/jcla.23416
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author Chen, Xuduan
Luo, Xiaofeng
Zu, Yanping
Issa, Hajji Ally
Li, Linlin
Ye, Hong
Yang, Ting
Hu, Jianda
Wei, Lixin
author_facet Chen, Xuduan
Luo, Xiaofeng
Zu, Yanping
Issa, Hajji Ally
Li, Linlin
Ye, Hong
Yang, Ting
Hu, Jianda
Wei, Lixin
author_sort Chen, Xuduan
collection PubMed
description BACKGROUND: Renal impairment (RI) is associated with poor survival in newly diagnosed multiple myeloma (MM) patients. Renal function recovery has been one of the main therapeutic goals in those patients. METHODS: The records from 393 newly diagnosed MM patients in our hospital between January 2012 and December 2016 were retrospectively analyzed. RI was defined as an eGFR < 40 mL/min according to the novel IMWG criteria. RI patients were categorized based on their renal function at diagnosis: severe RI: eGFR < 30 mL/min, and mild RI: 30 mL/min ≤ eGFR <40 mL/min. We explored whether RI, and particularly severe RI, was an adverse prognostic factor for survival, and investigated the impact of renal function recovery on survival. RESULTS: Severe RI, hemoglobin <100 g/L, LDH ≥ 245 U/L, hyperuricemia, 1q21 amplification, and lack of novel agent treatment were associated with decreased overall survival (OS). Severe RI patients with renal response had a median OS of 27 months compared with 18 months for those patients without renal response (P = .030), but their median OS was still significantly lower than that for patients without severe RI, which was 51 months. In severe RI patients, the overall renal response rate in bortezomib‐based regimens was significantly higher than that in nonbortezomib‐based regimens. CONCLUSION: Our results suggest that severe RI is an adverse prognostic factor for survival in newly diagnosed MM patients, restoration of renal function may improve survival, and bortezomib‐based regimens may be the preferred treatment in patients with severe RI.
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spelling pubmed-75212232020-09-30 Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients Chen, Xuduan Luo, Xiaofeng Zu, Yanping Issa, Hajji Ally Li, Linlin Ye, Hong Yang, Ting Hu, Jianda Wei, Lixin J Clin Lab Anal Research Articles BACKGROUND: Renal impairment (RI) is associated with poor survival in newly diagnosed multiple myeloma (MM) patients. Renal function recovery has been one of the main therapeutic goals in those patients. METHODS: The records from 393 newly diagnosed MM patients in our hospital between January 2012 and December 2016 were retrospectively analyzed. RI was defined as an eGFR < 40 mL/min according to the novel IMWG criteria. RI patients were categorized based on their renal function at diagnosis: severe RI: eGFR < 30 mL/min, and mild RI: 30 mL/min ≤ eGFR <40 mL/min. We explored whether RI, and particularly severe RI, was an adverse prognostic factor for survival, and investigated the impact of renal function recovery on survival. RESULTS: Severe RI, hemoglobin <100 g/L, LDH ≥ 245 U/L, hyperuricemia, 1q21 amplification, and lack of novel agent treatment were associated with decreased overall survival (OS). Severe RI patients with renal response had a median OS of 27 months compared with 18 months for those patients without renal response (P = .030), but their median OS was still significantly lower than that for patients without severe RI, which was 51 months. In severe RI patients, the overall renal response rate in bortezomib‐based regimens was significantly higher than that in nonbortezomib‐based regimens. CONCLUSION: Our results suggest that severe RI is an adverse prognostic factor for survival in newly diagnosed MM patients, restoration of renal function may improve survival, and bortezomib‐based regimens may be the preferred treatment in patients with severe RI. John Wiley and Sons Inc. 2020-07-25 /pmc/articles/PMC7521223/ /pubmed/32710448 http://dx.doi.org/10.1002/jcla.23416 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Chen, Xuduan
Luo, Xiaofeng
Zu, Yanping
Issa, Hajji Ally
Li, Linlin
Ye, Hong
Yang, Ting
Hu, Jianda
Wei, Lixin
Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title_full Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title_fullStr Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title_full_unstemmed Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title_short Severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
title_sort severe renal impairment as an adverse prognostic factor for survival in newly diagnosed multiple myeloma patients
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521223/
https://www.ncbi.nlm.nih.gov/pubmed/32710448
http://dx.doi.org/10.1002/jcla.23416
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