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First-Line Serplulimab in Extensive-Stage Small Cell Lung Cancer : Secondary Analysis of the ASTRUM-005 Phase 3 Randomized Clinical Trial
First-Line Serplulimab in Extensive-Stage Small Cell Lung Cancer: Secondary Analysis of the ASTRUM-005 Phase 3 Randomized Clinical Trial Key Points Question What are the long-term efficacy and safety outcomes of adding serplulimab to first-line chemotherapy for previously untreated extensive-stage small cell lung cancer (ES-SCLC)?
Savolitinib in MET -amplified gastric or gastroesophageal junction adenocarcinoma: a phase 2 trial
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Abstract MET proto-oncogene amplification (METamp) is associated with poor prognosis in gastric or gastroesophageal junction (G/GEJ) cancer. Currently, effective targeted therapies for G/GEJ cancer harboring METamp remain unavailable, and clinical evidence supporting the use of MET inhibitors in this disease population is limited. Here we report the results of a phase 2 study of savolitinib, an oral MET inhibitor, in patients with METamp G/GEJ cancer.
By Zhi Peng, Tianshu Liu, Hua Wang, Jufeng Wang, Hongli Liu, Feng Ye, Enxiao Li, Jun Zhang, Baorui Liu, Rongbo Lin, Aiping Zhou, Zhenyang Liu, Huiting Xu, Qiong Wang, Zuoxing Niu, Ying Yuan, Yanru Qin, Xiujuan Qu, Yuxian Bai, Ning Liu, Hailong Liu, Chunmei Bai, Yueyin Pan, Shubin Wang, Tao Wu, Qinghua Pan, Diansheng Zhong, Hongxia Lu, Junye Wang, Zhiyu Wang, Ting Deng, Hongfeng Gou, Xiwen Huang, Puhan Lu, Jie Yu, qian Xu, Linfang Wang, Yongxin Ren, Songhua Fan, Lin Shen, Mengyang Hong
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Nature
Verified
BRD4 orchestrates the metabolic-epigenetic regulation of GM-CSF expression and secretion to drive PD-L1⁺ macrophage-mediated immune evasion in triple-negative breast cancer | Oncogene
Abstract Immune checkpoint blockade targeting the PD-1/PD-L1 axis shows promise in triple-negative breast cancer (TNBC), yet durable responses are limited by immune escape. Here, we identified tumor-derived bromodomain-containing protein 4 (BRD4) as a critical mediator of tumor-associated macrophage (TAMs)-driven immune evasion in TNBC. Using syngeneic TNBC mouse models, we found that BRD4 promotes PD-L1 expression on TAMs by increasing GM-CSF production from tumor cells.
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