7262. Efficacy of catheter-based renal denervation in the absence of antihypertensive medications (SPYRAL HTN-OFF MED Pivotal): a multicentre, randomised, sham-controlled trial.
作者: Michael Böhm.;Kazuomi Kario.;David E Kandzari.;Felix Mahfoud.;Michael A Weber.;Roland E Schmieder.;Konstantinos Tsioufis.;Stuart Pocock.;Dimitris Konstantinidis.;James W Choi.;Cara East.;David P Lee.;Adrian Ma.;Sebastian Ewen.;Debbie L Cohen.;Robert Wilensky.;Chandan M Devireddy.;Janice Lea.;Axel Schmid.;Joachim Weil.;Tolga Agdirlioglu.;Denise Reedus.;Brian K Jefferson.;David Reyes.;Richard D'Souza.;Andrew S P Sharp.;Faisal Sharif.;Martin Fahy.;Vanessa DeBruin.;Sidney A Cohen.;Sandeep Brar.;Raymond R Townsend.; .
来源: Lancet. 2020年395卷10234期1444-1451页
Catheter-based renal denervation has significantly reduced blood pressure in previous studies. Following a positive pilot trial, the SPYRAL HTN-OFF MED (SPYRAL Pivotal) trial was designed to assess the efficacy of renal denervation in the absence of antihypertensive medications.
7275. Small molecules, big impact: 20 years of targeted therapy in oncology.
作者: Philippe L Bedard.;David M Hyman.;Matthew S Davids.;Lillian L Siu.
来源: Lancet. 2020年395卷10229期1078-1088页
The identification of molecular targets and the growing knowledge of their cellular functions have led to the development of small molecule inhibitors as a major therapeutic class for cancer treatment. Both multitargeted and highly selective kinase inhibitors are used for the treatment of advanced treatment-resistant cancers, and many have also achieved regulatory approval for early clinical settings as adjuvant therapies or as first-line options for recurrent or metastatic disease. Lessons learned from the development of these agents can accelerate the development of next-generation inhibitors to optimise the therapeutic index, overcome drug resistance, and establish combination therapies. The future of small molecule inhibitors is promising as there is the potential to investigate novel difficult-to-drug targets, to apply predictive non-clinical models to select promising drug candidates for human evaluation, and to use dynamic clinical trial interventions with liquid biopsies to deliver precision medicine.
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