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Personalising pancreas cancer treatment:When tissue is the issue 被引量:2
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作者 Katrin M Sjoquist Venessa T Chin +9 位作者 lorraine a chantrill Chelsie O'Connor Chris Hemmings David K Chang angela Chou Marina Pajic amber L Johns adnan M Nagrial andrew V Biankin Desmond Yip 《World Journal of Gastroenterology》 SCIE CAS 2014年第24期7849-7863,共15页
The treatment of advanced pancreatic cancer has not moved much beyond single agent gemcitabine until recently when protocols such as FOLFIRINOX(fluorouracil,leucovorin,irinotecan and oxaliplatin)and nab-paclitaxelgemc... The treatment of advanced pancreatic cancer has not moved much beyond single agent gemcitabine until recently when protocols such as FOLFIRINOX(fluorouracil,leucovorin,irinotecan and oxaliplatin)and nab-paclitaxelgemcitabine have demonstrated some improved outcomes.Advances in technology especially in massively parallel genome sequencing has progressed our understanding of the biology of pancreatic cancer especially the candidate signalling pathways that are involved in tumourogenesis and disease course.This has allowed identification of potentially actionable mutations that may be targeted by new biological agents.The heterogeneity of pancreatic cancer makes tumour tissue collection important with the aim of being able to personalise therapies for the individual as opposed to a one size fits all approach to treatment of the condition.This paper reviews the developments in this area of translational research and the ongoing clinical studies that will attempt to move this into the everyday oncology practice. 展开更多
关键词 PANCREATIC NEOPLASMS Molecular TARGETED therapy Ge
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