Cargando…

A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study

Background: Although neoadjuvant chemotherapy (NAC) has become the standard treatment option for muscle invasive bladder carcinoma (MIBC), its application is still limited because of the lack of biomarkers for NAC prediction. Methods: We conducted a territory multicenter real-world study to summariz...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Huihuang, Hu, Jiao, Zu, Xiongbing, Chen, Minfeng, Chen, Jinbo, Zou, Yihua, Deng, Ruoping, Qin, Gang, Li, Wenze, Tang, Jiansheng, Deng, Dingshan, Liu, Jinhui, Cheng, Chunliang, Cui, Yu, Ou, Zhenyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667090/
https://www.ncbi.nlm.nih.gov/pubmed/36406127
http://dx.doi.org/10.3389/fgene.2022.1047481
_version_ 1784831653379571712
author Li, Huihuang
Hu, Jiao
Zu, Xiongbing
Chen, Minfeng
Chen, Jinbo
Zou, Yihua
Deng, Ruoping
Qin, Gang
Li, Wenze
Tang, Jiansheng
Deng, Dingshan
Liu, Jinhui
Cheng, Chunliang
Cui, Yu
Ou, Zhenyu
author_facet Li, Huihuang
Hu, Jiao
Zu, Xiongbing
Chen, Minfeng
Chen, Jinbo
Zou, Yihua
Deng, Ruoping
Qin, Gang
Li, Wenze
Tang, Jiansheng
Deng, Dingshan
Liu, Jinhui
Cheng, Chunliang
Cui, Yu
Ou, Zhenyu
author_sort Li, Huihuang
collection PubMed
description Background: Although neoadjuvant chemotherapy (NAC) has become the standard treatment option for muscle invasive bladder carcinoma (MIBC), its application is still limited because of the lack of biomarkers for NAC prediction. Methods: We conducted a territory multicenter real-world study to summarize NAC practice in China and its associated clinicopathologic variables with NAC response. Then, we developed and validated a robust gene-based signature for accurate NAC prediction using weighted correlation network analysis (WGCNA), the least absolute shrinkage and selector operation (LASSO) algorithm, a multivariable binary logistic regression model, and immunohistochemistry (IHC). Results: In total, we collected 69 consecutive MIBC patients treated with NAC from four clinical centers. The application of NAC in the real world was relatively safe, with only two grade Ⅳ and seven grade Ⅲ AEs and no treatment-related deaths being reported. Among these patients, 16 patients gave up surgery after NAC, leaving 53 patients for further analysis. We divided them into pathological response and non-response groups and found that there were more patients with a higher grade and stage in the non-response group. Patients with a pathological response could benefit from a significant overall survival (OS) improvement. In addition, univariate and multivariate logistic analyses indicated that tumor grade and clinical T stage were both independent factors for predicting NAC response. Importantly, we developed and validated a five-gene-based risk score for extremely high predictive accuracy for NAC response. Conclusion: NAC was relatively safe and could significantly improve OS for MIBC patients in the real-world practice. Our five-gene-based risk score could guide personalized therapy and promote the application of NAC.
format Online
Article
Text
id pubmed-9667090
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-96670902022-11-17 A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study Li, Huihuang Hu, Jiao Zu, Xiongbing Chen, Minfeng Chen, Jinbo Zou, Yihua Deng, Ruoping Qin, Gang Li, Wenze Tang, Jiansheng Deng, Dingshan Liu, Jinhui Cheng, Chunliang Cui, Yu Ou, Zhenyu Front Genet Genetics Background: Although neoadjuvant chemotherapy (NAC) has become the standard treatment option for muscle invasive bladder carcinoma (MIBC), its application is still limited because of the lack of biomarkers for NAC prediction. Methods: We conducted a territory multicenter real-world study to summarize NAC practice in China and its associated clinicopathologic variables with NAC response. Then, we developed and validated a robust gene-based signature for accurate NAC prediction using weighted correlation network analysis (WGCNA), the least absolute shrinkage and selector operation (LASSO) algorithm, a multivariable binary logistic regression model, and immunohistochemistry (IHC). Results: In total, we collected 69 consecutive MIBC patients treated with NAC from four clinical centers. The application of NAC in the real world was relatively safe, with only two grade Ⅳ and seven grade Ⅲ AEs and no treatment-related deaths being reported. Among these patients, 16 patients gave up surgery after NAC, leaving 53 patients for further analysis. We divided them into pathological response and non-response groups and found that there were more patients with a higher grade and stage in the non-response group. Patients with a pathological response could benefit from a significant overall survival (OS) improvement. In addition, univariate and multivariate logistic analyses indicated that tumor grade and clinical T stage were both independent factors for predicting NAC response. Importantly, we developed and validated a five-gene-based risk score for extremely high predictive accuracy for NAC response. Conclusion: NAC was relatively safe and could significantly improve OS for MIBC patients in the real-world practice. Our five-gene-based risk score could guide personalized therapy and promote the application of NAC. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9667090/ /pubmed/36406127 http://dx.doi.org/10.3389/fgene.2022.1047481 Text en Copyright © 2022 Li, Hu, Zu, Chen, Chen, Zou, Deng, Qin, Li, Tang, Deng, Liu, Cheng, Cui and Ou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Li, Huihuang
Hu, Jiao
Zu, Xiongbing
Chen, Minfeng
Chen, Jinbo
Zou, Yihua
Deng, Ruoping
Qin, Gang
Li, Wenze
Tang, Jiansheng
Deng, Dingshan
Liu, Jinhui
Cheng, Chunliang
Cui, Yu
Ou, Zhenyu
A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title_full A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title_fullStr A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title_full_unstemmed A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title_short A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study
title_sort novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: results from a territory multicenter real-world study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667090/
https://www.ncbi.nlm.nih.gov/pubmed/36406127
http://dx.doi.org/10.3389/fgene.2022.1047481
work_keys_str_mv AT lihuihuang anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT hujiao anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT zuxiongbing anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chenminfeng anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chenjinbo anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT zouyihua anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT dengruoping anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT qingang anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT liwenze anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT tangjiansheng anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT dengdingshan anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT liujinhui anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chengchunliang anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT cuiyu anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT ouzhenyu anovelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT lihuihuang novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT hujiao novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT zuxiongbing novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chenminfeng novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chenjinbo novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT zouyihua novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT dengruoping novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT qingang novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT liwenze novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT tangjiansheng novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT dengdingshan novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT liujinhui novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT chengchunliang novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT cuiyu novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy
AT ouzhenyu novelsignaturetopredicttheneoadjuvantchemotherapyresponseofbladdercarcinomaresultsfromaterritorymulticenterrealworldstudy