Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA.
AD Stat Consulting, Guerneville, California, USA.
Clin Infect Dis. 2024 Jun 14;78(6):1473-1481. doi: 10.1093/cid/ciae043.
Novel treatments are needed for Staphylococcus aureus bacteremia, particularly for methicillin-resistant S. aureus (MRSA). Exebacase is a first-in-class antistaphylococcal lysin that is rapidly bactericidal and synergizes with antibiotics.
In Direct Lysis of Staph Aureus Resistant Pathogen Trial of Exebacase (DISRUPT), a superiority-design phase 3 study, patients with S. aureus bacteremia/endocarditis were randomly assigned to receive a single dose of intravenous exebacase or placebo in addition to standard-of-care antibiotics. The primary efficacy outcome was clinical response at day 14 in the MRSA population.
A total of 259 patients were randomized before the study was stopped for futility based on the recommendation of the unblinded Data Safety Monitoring Board. Clinical response rates at day 14 in the MRSA population (n = 97) were 50.0% (exebacase + antibiotics; 32/64) versus 60.6% (antibiotics alone; 20/33) (P = .392). Overall, rates of adverse events were similar across groups. No adverse events of hypersensitivity related to exebacase were reported.
Exebacase + antibiotics failed to improve clinical response at day 14 in patients with MRSA bacteremia/endocarditis. This result was unexpected based on phase 2 data that established proof-of-concept for exebacase + antibiotics in patients with MRSA bacteremia/endocarditis. In the antibiotics-alone group, the clinical response rate was higher than that seen in phase 2. Heterogeneity within the study population and a relatively small sample size in either the phase 2 or phase 3 studies may have increased the probability of imbalances in the multiple components of day 14 clinical outcome. This study provides lessons for future superiority studies in S. aureus bacteremia/endocarditis. Clinical Trials Registration.NCT04160468.
金黄色葡萄球菌菌血症需要新的治疗方法,特别是耐甲氧西林金黄色葡萄球菌(MRSA)。Exebacase 是一种首创的抗葡萄球菌溶菌素,具有快速杀菌作用,并与抗生素协同作用。
在 Exebacase 治疗金黄色葡萄球菌耐药病原体的直接裂解试验(DISRUPT)中,一项优效性设计的 3 期研究中,金黄色葡萄球菌菌血症/心内膜炎患者被随机分配接受单次静脉注射 Exebacase 或安慰剂,同时接受标准治疗抗生素。主要疗效终点是 MRSA 人群第 14 天的临床反应。
在研究因盲目数据安全监测委员会的建议而无效而停止之前,共随机分配了 259 名患者。MRSA 人群(n = 97)第 14 天的临床反应率分别为 50.0%(Exebacase + 抗生素;32/64)和 60.6%(单独使用抗生素;20/33)(P =.392)。总体而言,各组不良反应发生率相似。未报告与 Exebacase 相关的过敏反应不良事件。
Exebacase + 抗生素未能改善 MRSA 菌血症/心内膜炎患者第 14 天的临床反应。这一结果出乎意料,因为 2 期数据已确立了 Exebacase + 抗生素在 MRSA 菌血症/心内膜炎患者中的概念验证。在单独使用抗生素的组中,临床反应率高于 2 期研究。研究人群的异质性和 2 期或 3 期研究中相对较小的样本量可能增加了第 14 天临床结局的多个组成部分失衡的可能性。这项研究为未来金黄色葡萄球菌菌血症/心内膜炎的优效性研究提供了经验教训。临床试验注册。NCT04160468。