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Ibrutinib in B-cell lymphoma: single fighter might be enough?
BACKGROUND: In recent years, the B cell receptor (BCR) signaling pathway has become a “hot point” because it plays a critical role in B-cell proliferation and function. Bruton’s tyrosine kinase (BTK) is overexpressed in many subtypes of B-cell lymphoma as a downstream kinase in the BCR signaling pat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523373/ https://www.ncbi.nlm.nih.gov/pubmed/33005100 http://dx.doi.org/10.1186/s12935-020-01518-y |
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author | Xue, Chao Wang, Xin Zhang, Lingyan Qu, Qingyuan Zhang, Qian Jiang, Yujie |
author_facet | Xue, Chao Wang, Xin Zhang, Lingyan Qu, Qingyuan Zhang, Qian Jiang, Yujie |
author_sort | Xue, Chao |
collection | PubMed |
description | BACKGROUND: In recent years, the B cell receptor (BCR) signaling pathway has become a “hot point” because it plays a critical role in B-cell proliferation and function. Bruton’s tyrosine kinase (BTK) is overexpressed in many subtypes of B-cell lymphoma as a downstream kinase in the BCR signaling pathway. Ibrutinib, the first generation of BTK inhibitor, has shown excellent antitumor activity in both indolent and aggressive B-cell lymphoma. MAIN BODY: Ibrutinib monotherapy has been confirmed to be effective with a high response rate (RR) and well-tolerated in many B-cell lymphoma subgroups. To achieve much deeper and faster remission, combination strategies contained ibrutinib were conducted to evaluate their synergistic anti-tumor effect. CONCLUSIONS: For patients with indolent B-cell lymphoma, most of them respond well with ibrutinib monotherapy. Combination strategies contained ibrutinib might be a better choice to achieve deeper and faster remission in the treatment of aggressive subtypes of B-cell lymphoma. Further investigations on the long-term efficacy and safety of the ibrutinib will provide novel strategies for individualized treatment of B-cell lymphoma. |
format | Online Article Text |
id | pubmed-7523373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75233732020-09-30 Ibrutinib in B-cell lymphoma: single fighter might be enough? Xue, Chao Wang, Xin Zhang, Lingyan Qu, Qingyuan Zhang, Qian Jiang, Yujie Cancer Cell Int Review BACKGROUND: In recent years, the B cell receptor (BCR) signaling pathway has become a “hot point” because it plays a critical role in B-cell proliferation and function. Bruton’s tyrosine kinase (BTK) is overexpressed in many subtypes of B-cell lymphoma as a downstream kinase in the BCR signaling pathway. Ibrutinib, the first generation of BTK inhibitor, has shown excellent antitumor activity in both indolent and aggressive B-cell lymphoma. MAIN BODY: Ibrutinib monotherapy has been confirmed to be effective with a high response rate (RR) and well-tolerated in many B-cell lymphoma subgroups. To achieve much deeper and faster remission, combination strategies contained ibrutinib were conducted to evaluate their synergistic anti-tumor effect. CONCLUSIONS: For patients with indolent B-cell lymphoma, most of them respond well with ibrutinib monotherapy. Combination strategies contained ibrutinib might be a better choice to achieve deeper and faster remission in the treatment of aggressive subtypes of B-cell lymphoma. Further investigations on the long-term efficacy and safety of the ibrutinib will provide novel strategies for individualized treatment of B-cell lymphoma. BioMed Central 2020-09-29 /pmc/articles/PMC7523373/ /pubmed/33005100 http://dx.doi.org/10.1186/s12935-020-01518-y 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 | Review Xue, Chao Wang, Xin Zhang, Lingyan Qu, Qingyuan Zhang, Qian Jiang, Yujie Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title |
Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title_full |
Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title_fullStr |
Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title_full_unstemmed |
Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title_short |
Ibrutinib in B-cell lymphoma: single fighter might be enough? |
title_sort | ibrutinib in b-cell lymphoma: single fighter might be enough? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523373/ https://www.ncbi.nlm.nih.gov/pubmed/33005100 http://dx.doi.org/10.1186/s12935-020-01518-y |
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