A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer

Abstract The association between genetic variations and immunotherapy benefit has been widely recognized, while such evidence in gastrointestinal cancer remains limited. We analyzed the genomic profile of 227 immunotherapeutic gastrointestinal cancer patients treated with immunotherapy, from the Mem...

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Autores principales: Xi Jiao, Xin Wei, Shuang Li, Chang Liu, Huan Chen, Jifang Gong, Jian Li, Xiaotian Zhang, Xicheng Wang, Zhi Peng, Changsong Qi, Zhenghang Wang, Yujiao Wang, Yanni Wang, Na Zhuo, Henghui Zhang, Zhihao Lu, Lin Shen
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/af919b7c4d764432868744aa0e66f40a
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spelling oai:doaj.org-article:af919b7c4d764432868744aa0e66f40a2021-12-02T14:41:51ZA genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer10.1038/s41698-021-00172-52397-768Xhttps://doaj.org/article/af919b7c4d764432868744aa0e66f40a2021-05-01T00:00:00Zhttps://doi.org/10.1038/s41698-021-00172-5https://doaj.org/toc/2397-768XAbstract The association between genetic variations and immunotherapy benefit has been widely recognized, while such evidence in gastrointestinal cancer remains limited. We analyzed the genomic profile of 227 immunotherapeutic gastrointestinal cancer patients treated with immunotherapy, from the Memorial Sloan Kettering (MSK) Cancer Center cohort. A gastrointestinal immune prognostic signature (GIPS) was constructed using LASSO Cox regression. Based on this signature, patients were classified into two subgroups with distinctive prognoses (p < 0.001). The prognostic value of the GIPS was consistently validated in the Janjigian and Pender cohort (N = 54) and Peking University Cancer Hospital cohort (N = 92). Multivariate analysis revealed that the GIPS was an independent prognostic biomarker. Notably, the GIPS-high tumor was indicative of a T-cell-inflamed phenotype and immune activation. The findings demonstrated that GIPS was a powerful predictor of immunotherapeutic survival in gastrointestinal cancer and may serve as a potential biomarker guiding immunotherapy treatment decisions.Xi JiaoXin WeiShuang LiChang LiuHuan ChenJifang GongJian LiXiaotian ZhangXicheng WangZhi PengChangsong QiZhenghang WangYujiao WangYanni WangNa ZhuoHenghui ZhangZhihao LuLin ShenNature PortfolioarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Precision Oncology, Vol 5, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Xi Jiao
Xin Wei
Shuang Li
Chang Liu
Huan Chen
Jifang Gong
Jian Li
Xiaotian Zhang
Xicheng Wang
Zhi Peng
Changsong Qi
Zhenghang Wang
Yujiao Wang
Yanni Wang
Na Zhuo
Henghui Zhang
Zhihao Lu
Lin Shen
A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
description Abstract The association between genetic variations and immunotherapy benefit has been widely recognized, while such evidence in gastrointestinal cancer remains limited. We analyzed the genomic profile of 227 immunotherapeutic gastrointestinal cancer patients treated with immunotherapy, from the Memorial Sloan Kettering (MSK) Cancer Center cohort. A gastrointestinal immune prognostic signature (GIPS) was constructed using LASSO Cox regression. Based on this signature, patients were classified into two subgroups with distinctive prognoses (p < 0.001). The prognostic value of the GIPS was consistently validated in the Janjigian and Pender cohort (N = 54) and Peking University Cancer Hospital cohort (N = 92). Multivariate analysis revealed that the GIPS was an independent prognostic biomarker. Notably, the GIPS-high tumor was indicative of a T-cell-inflamed phenotype and immune activation. The findings demonstrated that GIPS was a powerful predictor of immunotherapeutic survival in gastrointestinal cancer and may serve as a potential biomarker guiding immunotherapy treatment decisions.
format article
author Xi Jiao
Xin Wei
Shuang Li
Chang Liu
Huan Chen
Jifang Gong
Jian Li
Xiaotian Zhang
Xicheng Wang
Zhi Peng
Changsong Qi
Zhenghang Wang
Yujiao Wang
Yanni Wang
Na Zhuo
Henghui Zhang
Zhihao Lu
Lin Shen
author_facet Xi Jiao
Xin Wei
Shuang Li
Chang Liu
Huan Chen
Jifang Gong
Jian Li
Xiaotian Zhang
Xicheng Wang
Zhi Peng
Changsong Qi
Zhenghang Wang
Yujiao Wang
Yanni Wang
Na Zhuo
Henghui Zhang
Zhihao Lu
Lin Shen
author_sort Xi Jiao
title A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
title_short A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
title_full A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
title_fullStr A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
title_full_unstemmed A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
title_sort genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/af919b7c4d764432868744aa0e66f40a
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