F2G, Ltd, Eccles, United Kingdom.
Talbot Advisors LLC, Anna Maria, Florida.
Clin Infect Dis. 2017 Jul 1;65(1):141-146. doi: 10.1093/cid/cix246.
From a public health perspective, new antibacterial agents should be evaluated and approved for use before widespread resistance to existing agents emerges. However, for multidrug-resistant pathogens, demonstration of superior efficacy of a new agent over a current standard-of-care agent is routinely feasible only when epidemic spread of these dangerous organisms has already occurred. One solution to enable proactive drug development is to evaluate new antibiotics with improved in vitro activity against MDR pathogens using recently updated guidelines for active control, noninferiority trials of selected severe infections caused by more susceptible pathogens. Such trials are feasible because they enroll patients with infections due to pathogens with a "usual drug resistance" phenotype that will be responsive to widely registered standard-of-care comparator antibiotics. Such anticipatory drug development has constructively reshaped the antibiotic pipeline and offers the best chance of making safe and efficacious antibiotics available to the public ahead of epidemic resistance.
从公共卫生的角度来看,在现有抗菌药物广泛产生耐药性之前,应该对新的抗菌药物进行评估和批准使用。然而,对于多药耐药病原体,只有在这些危险病原体已经出现流行传播的情况下,新的抗菌药物相对于现有标准治疗药物具有优越疗效的证明才是常规可行的。一种解决方法是使用最近更新的主动控制指南,对具有改善的体外活性的新型抗生素进行评估,以针对更易受影响的病原体引起的选定严重感染进行非劣效性试验。这种试验是可行的,因为它们招募的是患有感染的患者,这些感染是由具有“通常药物耐药性”表型的病原体引起的,这些病原体对抗生素标准治疗药物的反应良好。这种前瞻性药物开发建设性地重塑了抗生素研发管道,并为在流行耐药性出现之前为公众提供安全有效的抗生素提供了最佳机会。