Antibiotic Exposure Does Not Impact Immune Checkpoint Blockade Response in MSI-H/dMMR Metastatic Colorectal Cancer: A Single-Center Experience

医学 彭布罗利珠单抗 无容量 微卫星不稳定性 内科学 结直肠癌 肿瘤科 免疫检查点 临床终点 癌症 封锁 队列 相伴的 免疫疗法 临床试验 化学 生物化学 等位基因 受体 基因 微卫星
作者
Victoria Serpas Higbie,Jane E. Rogers,Hyunsoo Hwang,Wei Qiao,Lianchun Xiao,Arvind Dasari,Kerri Mola-Rudd,Van K. Morris,Robert A. Wolff,Kanwal Raghav,Ryan Huey,Christine M. Parseghian,Jason Willis,Scott Kopetz,Michael J. Overman,Benny Johnson
出处
期刊:Oncologist [Wiley]
卷期号:27 (11): 952-957 被引量:12
标识
DOI:10.1093/oncolo/oyac162
摘要

Abstract Background Immune checkpoint blockade (ICB) has improved outcomes for patients with microsatellite instability high (MSI-H)/deficient mismatch repair (dMMR) tumors. However, not all MSI-H/dMMR patients will exhibit the same ICB efficacy. Previous studies suggest that concomitant antibiotic use while receiving ICB may result in poorer outcomes. We aimed to evaluate this association in patients with MSI-H/dMMR metastatic colorectal cancer (mCRC). Materials and Methods A single-site, retrospective review of 57 patients with MSI-H/dMMR mCRC that received ICB was completed. Data collected included patient demographics, ICB information, and antibiotic use. Antibiotic exposure was considered from 90 days prior to ICB through 6 weeks after initiation. Primary endpoint was overall response rate (ORR). Results The majority of patients received pembrolizumab (27 [47%]) or nivolumab (17 [30%]) monotherapy as their ICB agent. Of the 57 patients, 19 (33.3%) had antibiotic exposure from 90 days prior to ICB initiation through 6 weeks after initiation with most (13 [68%]) having antibiotic use in the 30 days preceding ICB initiation. Similar ORRs were seen in both groups (P-value > .99). No difference was observed in OS (P-value .29) or PFS (P-value .36) between groups. Conclusion Our data show no association of lower response rates or survival in those MSI-H/dMMR patients with mCRC who receive antibiotics around the initiation of ICB. This information needs to be confirmed in a larger prospective cohort.

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