Paterson David L, Kinoshita Masahiro, Baba Takamichi, Echols Roger, Portsmouth Simon
Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Royal Brisbane and Women's Hospital Campus, Brisbane, Australia.
Shionogi & Co., Ltd., Osaka, Japan.
Infect Dis Ther. 2022 Apr;11(2):853-870. doi: 10.1007/s40121-022-00598-9. Epub 2022 Feb 20.
A post hoc, descriptive analysis of three prospective, randomised, controlled clinical studies investigating cefiderocol in gram-negative bacterial infections was conducted to assess its efficacy in patients with baseline bacteraemia.
Data from APEKS-cUTI (NCT02321800), APEKS-NP (NCT03032380) and CREDIBLE-CR (NCT02714595) studies were assessed individually. Patients received cefiderocol 2g, q8h, for 7-14 days or comparators (imipenem/cilastatin [APEKS-cUTI], meropenem [APEKS-NP] or best available therapy [BAT; CREDIBLE-CR]). Bacteraemia and clinical outcomes were assessed at early assessment (EA), end of treatment (EOT) and test of cure (TOC) for patients in the intention-to-treat populations with baseline blood samples positive for aerobic gram-negative species. Eradication, persistence or recurrence of baseline blood pathogen was confirmed from follow-up blood cultures; in the absence of follow-up blood cultures, clinical response, administration of additional antibiotics and vital status were used to assess bacteraemia outcome.
Of 885 patients randomised, 84 had bacteraemia and 89 (cefiderocol: 55, comparators: 34) gram-negative pathogens were isolated, namely Enterobacterales (n = 62) and non-fermenters (n = 27). At EA, on-therapy bacteraemia eradication rates in APEKS-cUTI, APEKS-NP and CREDIBLE-CR were 100% (19/19), 50.0% (4/8) and 72.0% (18/25) with cefiderocol. Corresponding rates for comparators were 77.8% (7/9), 100% (10/10) and 69.2% (9/13), respectively. Persistence in blood at EA was seen in six patients overall (cefiderocol: 3, comparators: 3); indeterminate responses were common (cefiderocol: 8, comparators: 3), usually due to lack of blood cultures. Clinical cure/improvement rates at EA in APEKS-cUTI, APEKS-NP and CREDIBLE-CR were 100% (19/19), 62.5% (5/8) and 64.0% (16/25) with cefiderocol. Corresponding rates for comparators were 77.8% (7/9), 90.0% (9/10) and 30.8% (4/13), respectively. Bacteraemia eradication rates with cefiderocol in APEKS-cUTI, APEKS-NP and CREDIBLE-CR were 89.5%, 37.5% and 60.0% at EOT and 78.9%, 12.5% and 44.0% at TOC.
This descriptive analysis suggests that cefiderocol may be a useful treatment option for gram-negative bacteraemia, including pathogens resistant to other antibiotics.
对三项研究头孢地尔在革兰氏阴性菌感染中应用的前瞻性、随机、对照临床研究进行事后描述性分析,以评估其在基线菌血症患者中的疗效。
分别评估来自APEKS-cUTI(NCT02321800)、APEKS-NP(NCT03032380)和CREDIBLE-CR(NCT02714595)研究的数据。患者接受2g头孢地尔,每8小时一次,共7 - 14天,或接受对照药物(亚胺培南/西司他丁[APEKS-cUTI]、美罗培南[APEKS-NP]或最佳可用治疗[BAT;CREDIBLE-CR])。对意向性治疗人群中基线血样需氧革兰氏阴性菌呈阳性的患者,在早期评估(EA)、治疗结束(EOT)和治愈检测(TOC)时评估菌血症和临床结局。通过随访血培养确认基线血源性病原体的根除、持续存在或复发;在没有随访血培养的情况下,使用临床反应、额外抗生素的使用和生命体征来评估菌血症结局。
在885例随机分组的患者中,84例有菌血症,分离出89株(头孢地尔:55株,对照药物:34株)革兰氏阴性病原体,即肠杆菌科(n = 62)和非发酵菌(n = 27)。在EA时,APEKS-cUTI、APEKS-NP和CREDIBLE-CR中使用头孢地尔治疗时菌血症根除率分别为100%(19/19)、50.0%(4/8)和72.0%(18/25)。对照药物的相应根除率分别为77.8%(7/9)、100%(10/10)和69.2%(9/13)。总体上有6例患者在EA时血中病原体持续存在(头孢地尔:3例,对照药物:3例);不确定反应很常见(头孢地尔:8例,对照药物:3例),通常是由于缺乏血培养。在APEKS-cUTI、APEKS-NP和CREDIBLE-CR中使用头孢地尔治疗时,EA时的临床治愈/改善率分别为100%(19/19)、62.5%(5/8)和64.0%(16/25)。对照药物的相应治愈率分别为77.8%(7/9)、90.0%(9/10)和30.8%(4/13)。在APEKS-cUTI、APEKS-NP和CREDIBLE-CR中,头孢地尔在EOT时的菌血症根除率分别为89.5%、37.5%和60.0%,在TOC时分别为78.9%、12.5%和44.0%。
该描述性分析表明,头孢地尔可能是革兰氏阴性菌血症的一种有效治疗选择,包括对其他抗生素耐药的病原体。