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Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis

Bortezomib-based regimens are widely used as induction therapy for multiple myeloma (MM). Unlike lenalidomide, the role of bortezomib in consolidation and maintenance therapy for MM is less clear. We performed a meta-analysis to evaluate the impact of bortezomib-based consolidation and maintenance t...

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Autores principales: Zhang, Shijia, Kulkarni, Amit A., Xu, Beibei, Chu, Haitao, Kourelis, Taxiarchis, Go, Ronald S., Wang, Michael L., Bachanova, Veronika, Wang, Yucai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060191/
https://www.ncbi.nlm.nih.gov/pubmed/32144237
http://dx.doi.org/10.1038/s41408-020-0298-1
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author Zhang, Shijia
Kulkarni, Amit A.
Xu, Beibei
Chu, Haitao
Kourelis, Taxiarchis
Go, Ronald S.
Wang, Michael L.
Bachanova, Veronika
Wang, Yucai
author_facet Zhang, Shijia
Kulkarni, Amit A.
Xu, Beibei
Chu, Haitao
Kourelis, Taxiarchis
Go, Ronald S.
Wang, Michael L.
Bachanova, Veronika
Wang, Yucai
author_sort Zhang, Shijia
collection PubMed
description Bortezomib-based regimens are widely used as induction therapy for multiple myeloma (MM). Unlike lenalidomide, the role of bortezomib in consolidation and maintenance therapy for MM is less clear. We performed a meta-analysis to evaluate the impact of bortezomib-based consolidation and maintenance therapy on survival outcomes and adverse events. PubMed, Web of Science, Embase databases, and major conference proceedings were searched for randomized controlled trials (RCTs) of bortezomib-based regimens as consolidation or maintenance therapy for MM. Ten RCTs enrolling 3147 patients were included in the meta-analysis. Bortezomib-based regimens were compared with regimens without bortezomib or observation. The meta-analysis suggested that bortezomib-based maintenance therapy improved progression-free survival (PFS; hazard ratio [HR] = 0.72, 95% CI 0.55–0.95, P = 0.02) and overall survival (OS; HR = 0.71, 95% CI 0.58–0.87, P = 0.001). Bortezomib-based consolidation therapy improved PFS (HR = 0.77, 95% CI 0.68–0.88, P < 0.001) but not OS (HR = 0.98, 95% CI 0.78–1.24, P = 0.87). Bortezomib-based consolidation/maintenance therapy led to a trend toward increased risk of grade ≥ 3 neurologic symptoms, gastrointestinal symptoms, and fatigue. More research is warranted to further assess the role of bortezomib-based consolidation and maintenance therapy for multiple myeloma.
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spelling pubmed-70601912020-03-19 Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis Zhang, Shijia Kulkarni, Amit A. Xu, Beibei Chu, Haitao Kourelis, Taxiarchis Go, Ronald S. Wang, Michael L. Bachanova, Veronika Wang, Yucai Blood Cancer J Article Bortezomib-based regimens are widely used as induction therapy for multiple myeloma (MM). Unlike lenalidomide, the role of bortezomib in consolidation and maintenance therapy for MM is less clear. We performed a meta-analysis to evaluate the impact of bortezomib-based consolidation and maintenance therapy on survival outcomes and adverse events. PubMed, Web of Science, Embase databases, and major conference proceedings were searched for randomized controlled trials (RCTs) of bortezomib-based regimens as consolidation or maintenance therapy for MM. Ten RCTs enrolling 3147 patients were included in the meta-analysis. Bortezomib-based regimens were compared with regimens without bortezomib or observation. The meta-analysis suggested that bortezomib-based maintenance therapy improved progression-free survival (PFS; hazard ratio [HR] = 0.72, 95% CI 0.55–0.95, P = 0.02) and overall survival (OS; HR = 0.71, 95% CI 0.58–0.87, P = 0.001). Bortezomib-based consolidation therapy improved PFS (HR = 0.77, 95% CI 0.68–0.88, P < 0.001) but not OS (HR = 0.98, 95% CI 0.78–1.24, P = 0.87). Bortezomib-based consolidation/maintenance therapy led to a trend toward increased risk of grade ≥ 3 neurologic symptoms, gastrointestinal symptoms, and fatigue. More research is warranted to further assess the role of bortezomib-based consolidation and maintenance therapy for multiple myeloma. Nature Publishing Group UK 2020-03-06 /pmc/articles/PMC7060191/ /pubmed/32144237 http://dx.doi.org/10.1038/s41408-020-0298-1 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
Zhang, Shijia
Kulkarni, Amit A.
Xu, Beibei
Chu, Haitao
Kourelis, Taxiarchis
Go, Ronald S.
Wang, Michael L.
Bachanova, Veronika
Wang, Yucai
Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title_full Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title_fullStr Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title_full_unstemmed Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title_short Bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
title_sort bortezomib-based consolidation or maintenance therapy for multiple myeloma: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060191/
https://www.ncbi.nlm.nih.gov/pubmed/32144237
http://dx.doi.org/10.1038/s41408-020-0298-1
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