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State of the art biological therapies in pancreatic cancer 被引量:3

State of the art biological therapies in pancreatic cancer
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摘要 Pancreatic ductal adenocarcinoma(PDAC) is one of the most lethal malignancies with a five-year survival rate of approximately 5%. Several target agents have been tested in PDAC, but almost all have failed to demonstrate efficacy in late phase clinical trials, despite the better understanding of PDAC molecular biology generated by large cancer sequencing initiatives in the past decade. Eroltinib(a small-molecule tyrosine-kinase inhibitor of epidermal growth factor receptor) plus gemcitabine is the only schedule with a biological agent approved for advanced pancreatic cancer, but it has resulted in a very modest survival benefit in unselected patients. In our work, we report a summary of the main clinical trials(closed and ongoing) that refer to biological therapy evaluation in pancreatic cancer treatment. Pancreatic ductal adenocarcinoma(PDAC) is one of the most lethal malignancies with a five-year survival rate of approximately 5%. Several target agents have been tested in PDAC, but almost all have failed to demonstrate efficacy in late phase clinical trials, despite the better understanding of PDAC molecular biology generated by large cancer sequencing initiatives in the past decade. Eroltinib(a small-molecule tyrosine-kinase inhibitor of epidermal growth factor receptor) plus gemcitabine is the only schedule with a biological agent approved for advanced pancreatic cancer, but it has resulted in a very modest survival benefit in unselected patients. In our work, we report a summary of the main clinical trials(closed and ongoing) that refer to biological therapy evaluation in pancreatic cancer treatment.
出处 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2016年第1期55-66,共12页 世界胃肠肿瘤学杂志(英文版)(电子版)
关键词 PANCREATIC cancer Molecular characterization TARGETED therapy EPIDERMAL growth factor receptorinhibitors EMBRYONIC pathway INHIBITORS Antiangiogenictherapies Pancreatic cancer Molecular characterization Targeted therapy Epidermal growth factor receptor inhibitors Embryonic pathway inhibitors Antiangiogenic therapies
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