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Network meta-analysis of targeted therapies for diffuse large B cell lymphoma

BACKGROUND: The purpose of this network meta-analysis of randomized controlled trials (RCTs) was to compare rank targeted therapies for patients with diffuse large B-cell lymphoma (DLBCL). METHODS: The PubMed, EmBase, and Cochrane library electronic databases were systematically searched throughout...

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Autores principales: Wang, Jie, Huang, Jun, Zeng, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733263/
https://www.ncbi.nlm.nih.gov/pubmed/33308179
http://dx.doi.org/10.1186/s12885-020-07715-2
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author Wang, Jie
Huang, Jun
Zeng, Qing
author_facet Wang, Jie
Huang, Jun
Zeng, Qing
author_sort Wang, Jie
collection PubMed
description BACKGROUND: The purpose of this network meta-analysis of randomized controlled trials (RCTs) was to compare rank targeted therapies for patients with diffuse large B-cell lymphoma (DLBCL). METHODS: The PubMed, EmBase, and Cochrane library electronic databases were systematically searched throughout December 2019. Direct and indirect evidence from relevant RCTs was identified for network meta-analysis. The pooled results for grade 3 or greater adverse events between targeted therapies and chemotherapy were calculated using a random-effects model. RESULTS: A total of 18 RCTs enrolling 8207 DLBCL patients were selected for the final meta-analysis. The results of the network analysis indicated that the addition of dacetuzumab (74.8%) to rituximab-based regimens or lenalidomide (77.1%) was associated with better therapeutic effects on overall survival, whereas dacetuzumab (80.4%) or bortezomib (70.8%) added to rituximab was most likely to improve events-free survival. Moreover, lenalidomide (93.8%) and I-tositumomab (77.2%) were associated with higher overall response rates. Finally, patients receiving targeted therapies were associated with an increased risk of diarrhea (RR: 2.63; 95%CI: 1.18–5.86; P = 0.019), and thrombocytopenia (RR: 1.41; 95%CI: 1.05–1.90; P = 0.023). CONCLUSIONS: This study provides the best treatment strategy for DLBCL patients in terms of overall survival, events-free survival, and overall response rate. The findings of this study require validation with further large-scale RCTs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-020-07715-2.
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spelling pubmed-77332632020-12-14 Network meta-analysis of targeted therapies for diffuse large B cell lymphoma Wang, Jie Huang, Jun Zeng, Qing BMC Cancer Research Article BACKGROUND: The purpose of this network meta-analysis of randomized controlled trials (RCTs) was to compare rank targeted therapies for patients with diffuse large B-cell lymphoma (DLBCL). METHODS: The PubMed, EmBase, and Cochrane library electronic databases were systematically searched throughout December 2019. Direct and indirect evidence from relevant RCTs was identified for network meta-analysis. The pooled results for grade 3 or greater adverse events between targeted therapies and chemotherapy were calculated using a random-effects model. RESULTS: A total of 18 RCTs enrolling 8207 DLBCL patients were selected for the final meta-analysis. The results of the network analysis indicated that the addition of dacetuzumab (74.8%) to rituximab-based regimens or lenalidomide (77.1%) was associated with better therapeutic effects on overall survival, whereas dacetuzumab (80.4%) or bortezomib (70.8%) added to rituximab was most likely to improve events-free survival. Moreover, lenalidomide (93.8%) and I-tositumomab (77.2%) were associated with higher overall response rates. Finally, patients receiving targeted therapies were associated with an increased risk of diarrhea (RR: 2.63; 95%CI: 1.18–5.86; P = 0.019), and thrombocytopenia (RR: 1.41; 95%CI: 1.05–1.90; P = 0.023). CONCLUSIONS: This study provides the best treatment strategy for DLBCL patients in terms of overall survival, events-free survival, and overall response rate. The findings of this study require validation with further large-scale RCTs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-020-07715-2. BioMed Central 2020-12-11 /pmc/articles/PMC7733263/ /pubmed/33308179 http://dx.doi.org/10.1186/s12885-020-07715-2 Text en © The Author(s) 2020 Open AccessThis 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 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wang, Jie
Huang, Jun
Zeng, Qing
Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title_full Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title_fullStr Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title_full_unstemmed Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title_short Network meta-analysis of targeted therapies for diffuse large B cell lymphoma
title_sort network meta-analysis of targeted therapies for diffuse large b cell lymphoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733263/
https://www.ncbi.nlm.nih.gov/pubmed/33308179
http://dx.doi.org/10.1186/s12885-020-07715-2
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