Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Xue, Chao, Wang, Xin, Zhang, Lingyan, Qu, Qingyuan, Zhang, Qian, Jiang, Yujie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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
_version_ 1783588374226927616
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
work_keys_str_mv AT xuechao ibrutinibinbcelllymphomasinglefightermightbeenough
AT wangxin ibrutinibinbcelllymphomasinglefightermightbeenough
AT zhanglingyan ibrutinibinbcelllymphomasinglefightermightbeenough
AT quqingyuan ibrutinibinbcelllymphomasinglefightermightbeenough
AT zhangqian ibrutinibinbcelllymphomasinglefightermightbeenough
AT jiangyujie ibrutinibinbcelllymphomasinglefightermightbeenough