Northeastern Ohio Universities Colleges of Medicine and Pharmacy, Rootstown, Ohio, USA.
Clin Infect Dis. 2010 Dec 15;51(12):1395-405. doi: 10.1086/657313. Epub 2010 Nov 10.
Ceftaroline, the active form of ceftaroline fosamil, is a broad-spectrum cephalosporin with bactericidal activity against pathogens causing community-acquired pneumonia (CAP), including Streptococcus pneumoniae. Ceftaroline was evaluated for the treatment of CAP in 2 randomized, double-blind, multicenter trials: Ceftaroline Community Acquired Pneumonia Trial versus Ceftriaxone in Hospitalized Patients (FOCUS) 1 and FOCUS 2.
Patients hospitalized (but not admitted to an intensive care unit) with Pneumonia Outcomes Research Team risk class III or IV CAP requiring intravenous therapy were randomized to ceftaroline 600 mg every 12 h or ceftriaxone 1 g every 24 h for 5-7 days. Patients in FOCUS 1 received 2 doses of oral clarithromycin 500 mg every 12 h on day 1.
In the individual trials, clinical cure rates in the clinically evaluable (CE) population for ceftaroline versus ceftriaxone were as follows: FOCUS 1, 86.6% vs 78.2% (difference, 8.4%; 95% confidence interval [CI], 1.4%-15.4%); FOCUS 2, 82.1% vs 77.2% (difference, 4.9%; 95% CI, -2.5% to 12.5%). In the integrated analysis, 614 patients received ceftaroline and 614 received ceftriaxone. Of the CE patients treated with ceftaroline, 84.3% achieved clinical cure, compared with 77.7% of ceftriaxone-treated patients (difference, 6.7%; 95% CI, 1.6%-11.8%). Clinical cure rates in the modified intent-to-treat efficacy population were 82.6% versus 76.6% for ceftaroline and ceftriaxone (difference, 6.0%; 95% CI, 1.4%-10.7%). Ceftaroline and ceftriaxone were well tolerated; rates of adverse events, serious adverse events, deaths, and premature discontinuations caused by an adverse event were similar in both treatment arms.
Ceftaroline was noninferior to ceftriaxone in the individual trials. In this integrated analysis, clinical cure rates for the ceftaroline group were numerically higher than those for the ceftriaxone group. Ceftaroline was well tolerated, with a safety profile similar to that of ceftriaxone.
头孢洛林是头孢洛林磷酸酯的活性形式,是一种具有杀菌活性的广谱头孢菌素,可治疗社区获得性肺炎(CAP),包括肺炎链球菌。头孢洛林已在 2 项随机、双盲、多中心试验中被评估用于 CAP 的治疗:社区获得性肺炎头孢洛林试验与住院患者头孢曲松(FOCUS)1 及 FOCUS 2。
患有肺炎结果研究团队风险分类 III 或 IV 级 CAP 且需要静脉治疗的住院(但未入住重症监护病房)患者被随机分配至头孢洛林 600mg 每 12 小时或头孢曲松 1g 每 24 小时,疗程 5-7 天。FOCUS 1 中的患者在第 1 天接受 2 次口服克拉霉素 500mg 每 12 小时。
在各个试验中,头孢洛林组与头孢曲松组在临床可评估(CE)人群中的临床治愈率分别为:FOCUS 1,86.6%比 78.2%(差异,8.4%;95%置信区间[CI],1.4%-15.4%);FOCUS 2,82.1%比 77.2%(差异,4.9%;95%CI,-2.5%至 12.5%)。在整合分析中,614 例患者接受了头孢洛林治疗,614 例患者接受了头孢曲松治疗。接受头孢洛林治疗的 CE 患者中,84.3%达到临床治愈,而接受头孢曲松治疗的患者为 77.7%(差异,6.7%;95%CI,1.6%-11.8%)。在改良意向治疗疗效人群中,头孢洛林组的临床治愈率为 82.6%,头孢曲松组为 76.6%(差异,6.0%;95%CI,1.4%-10.7%)。头孢洛林和头孢曲松均具有良好的耐受性;在这两个治疗组中,不良反应、严重不良反应、死亡和因不良反应而提前停药的发生率相似。
在各个试验中,头孢洛林与头孢曲松相比不劣效。在这项整合分析中,头孢洛林组的临床治愈率高于头孢曲松组。头孢洛林具有良好的耐受性,安全性与头孢曲松相似。