J
Jie Wang
Researcher at Peking University
Publications - 107
Citations - 6855
Jie Wang is an academic researcher from Peking University. The author has contributed to research in topics: Lung cancer & Medicine. The author has an hindex of 27, co-authored 83 publications receiving 6079 citations. Previous affiliations of Jie Wang include Peking Union Medical College.
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Journal ArticleDOI
Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study
Caicun Zhou,Yi-Long Wu,Gongyan Chen,Jifeng Feng,Xiaoqing Liu,Changli Wang,Shucai Zhang,Jie Wang,Songwen Zhou,Shengxiang Ren,Shun Lu,Li Zhang,Chengping Hu,Chunhong Hu,Yi Luo,Lei Chen,Ming Ye,Jian'An Huang,Xiuyi Zhi,Yiping Zhang,Qingyu Xiu,Jun Ma,Changxuan You +22 more
TL;DR: It is suggested that erlotinib is important for first-line treatment of patients with advanced EGFR mutation-positive NSCLC, and was associated with more favourable tolerability than standard chemotherapy.
Journal ArticleDOI
Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients
Xiaohui Ni,Xiaohui Ni,Minglei Zhuo,Zhe Su,Jianchun Duan,Yan Gao,Zhijie Wang,Chenghang Zong,Hua Bai,Alec R. Chapman,Jun Zhao,Liya Xu,Tongtong An,Qi Ma,Yuyan Wang,Meina Wu,Yu Sun,Shuhang Wang,Zhenxiang Li,Xiaodan Yang,Jun Yong,Xiao-Dong Su,Youyong Lu,Fan Bai,X. Sunney Xie,X. Sunney Xie,Jie Wang +26 more
TL;DR: The use of the recently developed multiple annealing and looping-based amplification cycles for whole-genome amplification of single CTCs from lung cancer patients are reported, finding that copy number variations (CNVs), one of the major genomic variations, are specific to cancer types, reproducible from cell to cell, and even from patient to patient.
Journal ArticleDOI
Icotinib versus gefitinib in previously treated advanced non-small-cell lung cancer (ICOGEN): a randomised, double-blind phase 3 non-inferiority trial
Yuankai Shi,Li Zhang,Xiaoqing Liu,Caicun Zhou,Shucai Zhang,Dong Wang,Qiang Li,Shukui Qin,Chunhong Hu,Yiping Zhang,Jianhua Chen,Ying Cheng,Jifeng Feng,Helong Zhang,Yong Song,Yi-Long Wu,Nong Xu,Jianying Zhou,Rongcheng Luo,Chunxue Bai,Ye-ning Jin,Wenchao Liu,Zhaohui Wei,Fenlai Tan,Yinxiang Wang,Lieming Ding,Hong Dai,Shunchang Jiao,Jie Wang,Li Liang,Weimin Zhang,Yan Sun +31 more
TL;DR: Icotinib was non-inferior to gefitinib in terms of progression-free survival and could be a new treatment option for pretreated patients with advanced non-small-cell lung cancer.
Journal ArticleDOI
Gefitinib plus chemotherapy versus placebo plus chemotherapy in EGFR-mutation-positive non-small-cell lung cancer after progression on first-line gefitinib (IMPRESS): a phase 3 randomised trial
Jean-Charles Soria,Yi-Long Wu,Kazuhiko Nakagawa,Sang We Kim,Jin Ji Yang,Myung-Ju Ahn,Jie Wang,James Chih-Hsin Yang,You Lu,Shinji Atagi,Santiago Ponce,Dae Ho Lee,Yunpeng Liu,Kiyotaka Yoh,Jianying Zhou,Xiaojin Shi,Alan Webster,Haiyi Jiang,Tony Mok +18 more
TL;DR: The IMPRESS trial as discussed by the authors evaluated the efficacy and safety of continuing gefitinib combined with chemotherapy versus chemotherapy alone in patients with EGFR-mutation-positive advanced NSCLC with acquired resistance to first-line gefinib.
Journal ArticleDOI
Intercalated combination of chemotherapy and erlotinib for patients with advanced stage non-small-cell lung cancer (FASTACT-2): a randomised, double-blind trial
Yi-Long Wu,Jin Soo Lee,Sumitra Thongprasert,Chong-Jen Yu,Li Zhang,Guia Ladrera,Vichien Srimuninnimit,Virote Sriuranpong,Jennifer Sandoval-Tan,Yunzhong Zhu,Meilin Liao,Caicun Zhou,Hongming Pan,V. Lee,Yuh Min Chen,Yuh Min Chen,Yan Sun,Benjamin Margono,Fatima Fuerte,Gee-Chen Chang,Kasan Seetalarom,Jie Wang,Ashley Cheng,Elisna Syahruddin,Xiaoping Qian,James Chung-Man Ho,Johan Kurnianda,Hsingjin Eugene Liu,Kate Jin,Matt Truman,Ilze Bara,Tony Mok +31 more
TL;DR: Intercalated chemotherapy and erlotinib is a viable first-line option for patients with non-small-cell lung cancer with EGFR mutation-positive disease or selected patients with unknown EGFR mutations status.