Targeted and novel therapy in advanced gastric cancer

被引:0
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作者
Julie H. Selim
Shagufta Shaheen
Wei-Chun Sheu
Chung-Tsen Hsueh
机构
[1] Loma Linda University,School of Pharmacy
[2] Stanford Cancer Center,Division of Oncology
[3] Richmond University Medical Center,Department of Internal Medicine
[4] Loma Linda University,Division of Medical Oncology and Hematology, Department of Medicine
关键词
Gastric cancer; Targeted therapy; Human epidermal growth factor receptor 2; Programmed death-1; Vascular endothelial growth factor receptor 2;
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摘要
The systemic treatment options for advanced gastric cancer (GC) have evolved rapidly in recent years. We have reviewed the recent data of clinical trial incorporating targeted agents, including inhibitors of angiogenesis, human epidermal growth factor receptor 2 (HER2), mesenchymal–epithelial transition, epidermal growth factor receptor, mammalian target of rapamycin, claudin-18.2, programmed death-1 and DNA. Addition of trastuzumab to platinum-based chemotherapy has become standard of care as front-line therapy in advanced GC overexpressing HER2. In the second-line setting, ramucirumab with paclitaxel significantly improves overall survival compared to paclitaxel alone. For patients with refractory disease, apatinib, nivolumab, ramucirumab and TAS-102 have demonstrated single-agent activity with improved overall survival compared to placebo alone. Pembrolizumab has demonstrated more than 50% response rate in microsatellite instability-high tumors, 15% response rate in tumors expressing programmed death ligand 1, and non-inferior outcome in first-line treatment compared to chemotherapy. This review summarizes the current state and progress of research on targeted therapy for advanced GC.
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