10 Papers
15 Citations
Xu Li is an academic researcher from Peking Union Medical College. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 1, co-authored 3 publications.
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Papers
Clinical analysis of 64 patients with lung-cancer-associated hypercalcemia
TL;DR: After correction, moderate and severe elevations of hypercalcemia and abnormal elevation of alkaline phosphatase levels were shown to be significant factors shortening patients' survival time.
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TP53 and LRP1B Co-Wild Predicts Improved Survival for Patients with LUSC Receiving Anti-PD-L1 Immunotherapy
Jiangyong Yu,Zaiwen Fan,Zhi Rui Zhou,Ping Zhang,Jing Bai,Xu Li,Min Tang,N. Fan,Xiao-nan Wu,Xin Nie,Xiaoyan Chen,Di Ma,Xi Chen,Liang Cui,Xuefeng Xia,Ling Yang,Xin Yi,Lin Li +17 more
TL;DR: TP53/LRP1B co-wild LUSC conferred an elevated response rate in anti-PD-L1 therapy and improved survival, which was associated with a chromosome-stable phenotype and an activated immune microenvironment.
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Prognostic and predictive impact of molecular tumor burden index in non-small cell lung cancer patients.
Fan Yang,Min Tang,Liang Cui,Jing Bai,Jiangyong Yu,Jiayi Gao,Xin Nie,Xu Li,Xue-ming Xia,Xin Yi,Ping Zhang,Lin Li +11 more
TL;DR: This study aimed to investigate the feasibility of molecular tumor burden index in circulating tumor DNA (ctDNA) as a predictor for immunotherapy in patients with NSCLC.
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[Clinical Research on Albumin-bound Paclitaxel-based Therapy in Advanced Lung Cancer].
TL;DR: In this paper, albumin-bound paclitaxel was shown to be effective and well tolerated in the treatment of advanced lung cancer including all histological subtypes, and the most common adverse reactions were hematologic toxicities and were all manageable.
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Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
Feifan Xiao,Bingbing Wu,Chenbin Dong,Guoqiang Cheng,Yun Cao,Laishuan Wang,Xinran Dong,Yulan Lu,Lin Yang,Liping Chen,Long Li,Xinnian Pan,Qiufen Wei,Deyi Zhuang,Dong-shen Chen,Zhaoqing Yin,Qi Ni,Ren-chao Liu,Suzhen Xu,Gang Liu,Ping Zhang,Yanyan Qian,Xu Li,Xiaomin Peng,Yao Wang,Huijun Wang,Wenhao Zhou +26 more
TL;DR: A high incidence of genetic causes in critically ill neonates with CADs is identified, with a combination of single-nucleotide variations and CNVs among the genetic causes of CAD.
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