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TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients

Primary testicular lymphoma (PTL), often appearing as focal masses in the scrotum and epididymides, is the most frequent testicular tumor in aged men. Although MYD88 and CD79B mutations were the most common genetic alterations observed, the gene mutation landscape of PTL remains poorly defined. In t...

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Autores principales: Wang, Xinfeng, Xu, Xiaoyu, Cai, Wenzhi, Bao, Haiyan, Huang, Hongming, Liu, Yifei, Yang, Xi, Ruan, Changgeng, Wu, Depei, Shen, Hongjie, Chen, Suning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164167/
https://www.ncbi.nlm.nih.gov/pubmed/32322395
http://dx.doi.org/10.1186/s40364-020-00189-1
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author Wang, Xinfeng
Xu, Xiaoyu
Cai, Wenzhi
Bao, Haiyan
Huang, Hongming
Liu, Yifei
Yang, Xi
Ruan, Changgeng
Wu, Depei
Shen, Hongjie
Chen, Suning
author_facet Wang, Xinfeng
Xu, Xiaoyu
Cai, Wenzhi
Bao, Haiyan
Huang, Hongming
Liu, Yifei
Yang, Xi
Ruan, Changgeng
Wu, Depei
Shen, Hongjie
Chen, Suning
author_sort Wang, Xinfeng
collection PubMed
description Primary testicular lymphoma (PTL), often appearing as focal masses in the scrotum and epididymides, is the most frequent testicular tumor in aged men. Although MYD88 and CD79B mutations were the most common genetic alterations observed, the gene mutation landscape of PTL remains poorly defined. In this study, we identified 1326 mutations involving 311 genes or regions in 90 PTL patients through next-generation sequencing (NGS). PTL patients with the TBL1XR1 mutation, irrespective of treatment therapy, had an inferior overall survival (OS) than TBL1XR1 WT (wild type) patients (p = 0.045). Moreover, patients with this mutation, treated with a CHOP regimen (CTX 750 mg/m(2) iv, d1,8 ADM 50 mg/m(2) iv, d1 VCR 1.4 mg/m(2) iv, d1 PDN 100 mg/m(2) po d1–5), had a poorer OS (p = 0.019). In addition, such patients were prone to have a more intensive infiltration of tumors (p = 0.025, x(2) = 4.890). Thus, we speculated that patients with a TBL1XR1 mutation have poorer prognosis, partly due to greater invasion and infiltration of tumors. Our results suggest that the TBL1XR1 mutation can be used as an indicator to predict the prognosis of PTL and can be employed as a promising new target for treatment of PTL in the future.
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spelling pubmed-71641672020-04-22 TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients Wang, Xinfeng Xu, Xiaoyu Cai, Wenzhi Bao, Haiyan Huang, Hongming Liu, Yifei Yang, Xi Ruan, Changgeng Wu, Depei Shen, Hongjie Chen, Suning Biomark Res Letter to the Editor Primary testicular lymphoma (PTL), often appearing as focal masses in the scrotum and epididymides, is the most frequent testicular tumor in aged men. Although MYD88 and CD79B mutations were the most common genetic alterations observed, the gene mutation landscape of PTL remains poorly defined. In this study, we identified 1326 mutations involving 311 genes or regions in 90 PTL patients through next-generation sequencing (NGS). PTL patients with the TBL1XR1 mutation, irrespective of treatment therapy, had an inferior overall survival (OS) than TBL1XR1 WT (wild type) patients (p = 0.045). Moreover, patients with this mutation, treated with a CHOP regimen (CTX 750 mg/m(2) iv, d1,8 ADM 50 mg/m(2) iv, d1 VCR 1.4 mg/m(2) iv, d1 PDN 100 mg/m(2) po d1–5), had a poorer OS (p = 0.019). In addition, such patients were prone to have a more intensive infiltration of tumors (p = 0.025, x(2) = 4.890). Thus, we speculated that patients with a TBL1XR1 mutation have poorer prognosis, partly due to greater invasion and infiltration of tumors. Our results suggest that the TBL1XR1 mutation can be used as an indicator to predict the prognosis of PTL and can be employed as a promising new target for treatment of PTL in the future. BioMed Central 2020-04-17 /pmc/articles/PMC7164167/ /pubmed/32322395 http://dx.doi.org/10.1186/s40364-020-00189-1 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 Letter to the Editor
Wang, Xinfeng
Xu, Xiaoyu
Cai, Wenzhi
Bao, Haiyan
Huang, Hongming
Liu, Yifei
Yang, Xi
Ruan, Changgeng
Wu, Depei
Shen, Hongjie
Chen, Suning
TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title_full TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title_fullStr TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title_full_unstemmed TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title_short TBL1XR1 mutation predicts poor outcome in primary testicular diffuse large B-cell lymphoma patients
title_sort tbl1xr1 mutation predicts poor outcome in primary testicular diffuse large b-cell lymphoma patients
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164167/
https://www.ncbi.nlm.nih.gov/pubmed/32322395
http://dx.doi.org/10.1186/s40364-020-00189-1
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