Braun Avery, Deng Mengying, Hasler Jill S, Bukavina Laura, Handorf Elizabeth, Abbosh Philip H
Department of Urologic Surgery, University of California Davis, 4860 Y Street, Suite 3500, Sacramento, CA, 95817, USA.
Biostatistics and Bioinformatics, Fox Chase Cancer Center, Philadelphia, PA, 19111, USA.
BMC Med. 2025 Feb 25;23(1):117. doi: 10.1186/s12916-024-03786-1.
Antibiotic therapy (ABT)-induced dysbiosis may affect the efficacy of immune checkpoint inhibitors (ICI) therapy. We investigated the association between ABT and real-world overall survival (rwOS) and progression-free survival (rwPFS) in patients with metastatic urothelial carcinoma (mUC) receiving ICI or cisplatin-based chemotherapy (CIS).
Three thousand, one hundred seventy-nine patients were included from a nationwide electronic health record-derived de-identified database. Three-month landmark Kaplan-Meier methods and log-rank tests were used to estimate rwOS/PFS between treatment modalities based on ABT groups (stratified by exposure, timing, excretion mode, and administration route). Cox proportional models with time-varying coefficients were used to investigate the associations between ABT, treatment modality, and rwOS/PFS.
A total of 402 (27.1%) ICI and 655 (38.6%) CIS patients received ABT (p < 0.001). ICI receipt (OR 0.65, p < 0.001) and advanced age (OR 0.98, p < 0.001) were associated with lower ABT use. ICI exclusive findings included a negative correlation with rwOS in patients who received post-treatment initiated (ICI median: pre-13.2 vs post-7.9 vs none-13.3 months; p = 0.009), oral (median oral-9.6 vs none-13.3 months, p = 0.03), and renally cleared (median renal-9.9 vs none-13.3 months, p = 0.04) ABT. ABT's effect was negatively associated with rwOS in ICI patients within first 6 months (HR 1.36, 95% CI 1.107-1.74, p = 0.01) but not thereafter (p = 0.7).
This study identified a potential ICI-specific negative correlation between ABT and rwOS in patients with mUC, specifically those exposed to ABT pills and receipt before treatment initiation. These results emphasize the importance of antibiotic stewardship and continued investigation of the role of gut microbiome in mUC treatment efficacy.
抗生素治疗(ABT)引起的菌群失调可能会影响免疫检查点抑制剂(ICI)治疗的疗效。我们调查了接受ICI或基于顺铂的化疗(CIS)的转移性尿路上皮癌(mUC)患者中ABT与实际总生存期(rwOS)和无进展生存期(rwPFS)之间的关联。
从全国性的电子健康记录衍生的去识别数据库中纳入了3179例患者。采用三个月的标志性Kaplan-Meier方法和对数秩检验,根据ABT组(按暴露、时间、排泄方式和给药途径分层)估计不同治疗方式之间的rwOS/PFS。使用具有时变系数的Cox比例模型来研究ABT、治疗方式和rwOS/PFS之间的关联。
共有402例(27.1%)ICI患者和655例(38.6%)CIS患者接受了ABT(p<0.001)。接受ICI治疗(比值比0.65,p<0.001)和高龄(比值比0.98,p<0.001)与较低的ABT使用相关。ICI的单独研究结果包括,接受治疗后开始使用ABT的患者的rwOS呈负相关(ICI中位数:治疗前13.2个月 vs 治疗后7.9个月 vs 未使用13.3个月;p=0.009)、口服ABT(中位数口服9.6个月 vs 未使用13.3个月,p=0.03)以及经肾脏清除的ABT(中位数经肾脏9.9个月 vs 未使用13.3个月,p=0.04)。在ICI患者中,ABT的作用在前6个月与rwOS呈负相关(风险比1.36,95%置信区间1.107-1.74,p=0.01),但此后无相关性(p=0.7)。
本研究确定了mUC患者中ABT与rwOS之间潜在的ICI特异性负相关,特别是那些服用ABT药丸且在治疗开始前接受治疗的患者。这些结果强调了抗生素管理的重要性,并持续研究肠道微生物群在mUC治疗疗效中的作用。