Cren Pierre-Yves, Bertrand Nicolas, Le Deley Marie-Cécile, Génin Michaël, Mortier Laurent, Odou Pascal, Penel Nicolas, Chazard Emmanuel
CERIM, ULR 2694 METRICS, Univ. Lille, CHU Lille, Lille, France.
Methodology and Biostatistics Unit, Centre Oscar Lambret, Lille, France.
Oncoimmunology. 2020 Nov 22;9(1):1846914. doi: 10.1080/2162402X.2020.1846914.
: The gut microbiota has a key role in the regulation of the immune system. Disruption of the gut microbiota's composition by antibiotics might significantly affect the efficacy of immune checkpoint inhibitors. In a study of patients treated with ipilimumab, we sought to assess the relationship between overall survival and in-hospital antibiotic administration. : Patients having been treated with ipilimumab between January 2012 and November 2014 were selected from the French National Hospital Discharge Summary Database. Exposure to antibiotics was defined as the presence of a hospital stay with a documented systemic bacterial infection in the 2 months before or the month after initiation of the patient's first ever course of ipilimumab. The primary outcome was overall survival. : We studied 43,124 hospital stays involving 1585 patients from 97 centers. All patients had received ipilimumab monotherapy for advanced melanoma. Overall, 117 of the 1585 patients (7.4%) were documented as having received systemic antibiotic therapy in hospital during the defined exposure period. The median overall survival time was shorter in patients with infection (6.3 months, vs. 15.4 months in patients without an infection; hazard ratio (HR) = 1.88, 95% confidence interval [1.46; 2.43], = 10). In a multivariate analysis adjusted for covariates, infection was still significantly associated with overall survival (HR = 1.68, [1.30; 2.18], = 10). : In patients treated with ipilimumab for advanced melanoma, infection, and antibiotic administration in hospital at around the time of the patient's first ever course of ipilimumab appears to be associated with significantly lower clinical benefit.
肠道微生物群在免疫系统调节中起关键作用。抗生素破坏肠道微生物群的组成可能会显著影响免疫检查点抑制剂的疗效。在一项针对接受伊匹单抗治疗的患者的研究中,我们试图评估总生存期与住院期间抗生素使用之间的关系。:从法国国家医院出院摘要数据库中选取2012年1月至2014年11月期间接受伊匹单抗治疗的患者。抗生素暴露定义为在患者首次接受伊匹单抗治疗前2个月或治疗后1个月内有记录的系统性细菌感染的住院情况。主要结局是总生存期。:我们研究了来自97个中心的1585例患者的43124次住院情况。所有患者均接受伊匹单抗单药治疗晚期黑色素瘤。总体而言,1585例患者中有117例(7.4%)在规定的暴露期内有住院接受系统性抗生素治疗的记录。感染患者的中位总生存时间较短(6.3个月,无感染患者为15.4个月;风险比(HR)=1.88,95%置信区间[1.46;2.43],P=0.001)。在对协变量进行调整的多变量分析中,感染仍与总生存期显著相关(HR=1.68,[1.30;2.18],P=0.001)。:在接受伊匹单抗治疗晚期黑色素瘤的患者中,在患者首次接受伊匹单抗治疗前后住院期间的感染和抗生素使用似乎与显著更低的临床获益相关。