2359. Fractional flow reserve versus angiography for guidance of PCI in patients with multivessel coronary artery disease (FAME): 5-year follow-up of a randomised controlled trial.
作者: Lokien X van Nunen.;Frederik M Zimmermann.;Pim A L Tonino.;Emanuele Barbato.;Andreas Baumbach.;Thomas Engstrøm.;Volker Klauss.;Philip A MacCarthy.;Ganesh Manoharan.;Keith G Oldroyd.;Peter N Ver Lee.;Marcel Van't Veer.;William F Fearon.;Bernard De Bruyne.;Nico H J Pijls.; .
来源: Lancet. 2015年386卷10006期1853-60页
In the Fractional Flow Reserve Versus Angiography for Multivessel Evaluation (FAME) study, fractional flow reserve (FFR)-guided percutaneous coronary intervention (PCI) improved outcome compared with angiography-guided PCI for up to 2 years of follow-up. The aim in this study was to investigate whether the favourable clinical outcome with the FFR-guided PCI in the FAME study persisted over a 5-year follow-up.
2360. Nasopharyngeal carcinoma.
作者: Melvin L K Chua.;Joseph T S Wee.;Edwin P Hui.;Anthony T C Chan.
来源: Lancet. 2016年387卷10022期1012-1024页
Epidemiological trends during the past decade suggest that although incidence of nasopharyngeal carcinoma is gradually declining, even in endemic regions, mortality from the disease has fallen substantially. This finding is probably a result of a combination of lifestyle modification, population screening coupled with better imaging, advances in radiotherapy, and effective systemic agents. In particular, intensity-modulated radiotherapy has driven the improvement in tumour control and reduction in toxic effects in survivors. Clinical use of Epstein-Barr virus (EBV) as a surrogate biomarker in nasopharyngeal carcinoma continues to increase, with quantitative assessment of circulating EBV DNA used for population screening, prognostication, and disease surveillance. Randomised trials are investigating the role of EBV DNA in stratification of patients for treatment intensification and deintensification. Among the exciting developments in nasopharyngeal carcinoma, vascular endothelial growth factor inhibition and novel immunotherapies targeted at immune checkpoint and EBV-specific tumour antigens offer promising alternatives to patients with metastatic disease.
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