Taioli Emanuela, Flores Raja M, Abdelhamid Arwa, Untalan Matthew, Ivic-Pavlicic Tara, Tuminello Stephanie
Institute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Thoracic Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.
JTO Clin Res Rep. 2024 Jul 31;5(12):100710. doi: 10.1016/j.jtocrr.2024.100710. eCollection 2024 Dec.
Immunotherapy has improved survival in patients with advanced NSCLC. Efficacy may decrease when patients are treated with antibiotics, possibly due to gut microbiome disruption, but few studies have investigated this using real-world, patient-level populations in the United States.
We have analyzed antibiotic use in patients with stage IV first, primary NSCLC diagnosed in 2015 and treated with chemotherapy or chemoimmunotherapy, drawn from the Surveillance, Epidemiology, and End Results-Medicare data set. Patients had to have continuous part A, part B, and part D Medicare coverage. Survival was determined through Kaplan-Meier and Cox proportional hazards models. All data analyses were performed using SAS.
The study included 788 patients, 440 (56%) of whom received antibiotics within 2 months before or after starting systemic treatment. The median follow-up time was 11.64 months. There was a statistically significant difference in survival for patients who received antibiotics ( = 0.007) and who had more than 1 round of antibiotics versus zero or 1 round ( < 0.0001). After adjustment, receipt of antibiotics (hazard ratio [HR]: 1.17, 95% confidence interval [CI]: 0.99-1.37) and receipt of multiple rounds of antibiotics (HR: 1.35, 95% CI: 1.14-1.60) were statistically significantly associated with worse survival. Among just those receiving chemoimmunotherapy (n = 203; 26%), there was still an increased risk of death for those receiving multiple antibiotic rounds (HR: 1.52, 95% CI: 1.09-2.13).
Antibiotic use concurrent with chemoimmunotherapy seems to be associated with worse survival. This is more pronounced when more cycles of antibiotics are given.
STUDY-19-00500.
免疫疗法已提高了晚期非小细胞肺癌(NSCLC)患者的生存率。患者接受抗生素治疗时疗效可能会降低,这可能是由于肠道微生物群受到破坏,但很少有研究在美国使用真实世界的患者层面人群对此进行调查。
我们分析了2015年诊断为IV期原发性NSCLC并接受化疗或化疗免疫疗法的患者的抗生素使用情况,数据来自监测、流行病学和最终结果-医疗保险数据集。患者必须拥有连续的A部分、B部分和D部分医疗保险。通过Kaplan-Meier和Cox比例风险模型确定生存率。所有数据分析均使用SAS进行。
该研究纳入了788名患者,其中440名(56%)在开始全身治疗前或后2个月内接受了抗生素治疗。中位随访时间为11.64个月。接受抗生素治疗的患者与接受超过1轮抗生素治疗的患者与接受零轮或1轮抗生素治疗的患者相比,生存率存在统计学显著差异(P = 0.007)(P < 0.0001)。调整后,接受抗生素治疗(风险比[HR]:1.17,95%置信区间[CI]:0.99 - 1.37)和接受多轮抗生素治疗(HR:1.35,95% CI:1.14 - 1.60)与较差的生存率在统计学上显著相关。仅在接受化疗免疫疗法的患者中(n = 203;26%),接受多轮抗生素治疗的患者死亡风险仍然增加(HR:1.52,95% CI:1.09 - 2.13)。
与化疗免疫疗法同时使用抗生素似乎与较差的生存率相关。当给予更多周期的抗生素时,这种情况更为明显。
STUDY - 19 - 00500