Association between antibiotic use, immune-related adverse events, and efficacy of immunotherapy in esophageal squamous cell carcinoma.
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OpenAlex 토픽 ·
Esophageal Cancer Research and Treatment
Cancer Immunotherapy and Biomarkers
Inflammatory Biomarkers in Disease Prognosis
[INTRODUCTION] Immune checkpoint inhibitors (ICIs) are essential for treating esophageal squamous cell carcinoma (ESCC).
- p-value p = 0.029
- p-value p = 0.0145
- 95% CI 2.5-5.3
APA
Tomoaki Shirakawa, Hiroo Imai, et al. (2026). Association between antibiotic use, immune-related adverse events, and efficacy of immunotherapy in esophageal squamous cell carcinoma.. International journal of clinical oncology. https://doi.org/10.1007/s10147-026-03036-9
MLA
Tomoaki Shirakawa, et al.. "Association between antibiotic use, immune-related adverse events, and efficacy of immunotherapy in esophageal squamous cell carcinoma.." International journal of clinical oncology, 2026.
PMID
42043497 ↗
Abstract 한글 요약
[INTRODUCTION] Immune checkpoint inhibitors (ICIs) are essential for treating esophageal squamous cell carcinoma (ESCC). As antibiotics (Abx) may reduce ICI efficacy, and immune-related adverse events (irAEs) relate to better outcomes, we investigated their association.
[PATIENTS AND METHODS] We retrospectively analyzed 121 advanced or metastatic ESCC patients treated with ICIs, assessing outcomes based on Abx use and irAEs.
[RESULTS] Forty-one patients (33.9%) were in the Abx (+) group, showing a significantly shorter median progression-free survival (PFS) (2.5 vs. 6.5 months; p = 0.029) and lower disease control rate (36.8% vs. 60.9%; p = 0.0145) than those in the Abx (-) group. irAEs were less frequent in the Abx (+) group (29.3% vs. 58.8%; p = 0.0037). The positive impact of irAEs on ICI efficacy was significant in overall population [irAE(-) vs. irAE(+): PFS, 4.4 months (95% CI 2.5-5.3) vs. 8.8 months (95% CI 5.9-13.7); log-rank p = 0.001; Hazard ratio (HR) 1.76, 95% CI 1.14-2.74; p = 0.011; overall survival (OS), 10.6 months (95% CI 7.0-13.1) vs. 18.1 months (95% CI 9.2-25.9); log-rank p = 0.043; HR 1.61, 95% CI 1.01-2.55; p = 0.046] but diminished if received Abx. Notably, the Abx (-)/irAE (+) group had the best outcomes, while the Abx (+)/irAE (-) group had the worst PFS (8.7 vs. 2.4 months; HR 2.07; p = 0.011) and OS (18.1 and 6.8 months; HR 1.89; p = 0.036).
[CONCLUSION] Antibiotic use was linked to reduced ICI efficacy and fewer irAEs, suggesting impaired immune activation in ESCC patients.
[PATIENTS AND METHODS] We retrospectively analyzed 121 advanced or metastatic ESCC patients treated with ICIs, assessing outcomes based on Abx use and irAEs.
[RESULTS] Forty-one patients (33.9%) were in the Abx (+) group, showing a significantly shorter median progression-free survival (PFS) (2.5 vs. 6.5 months; p = 0.029) and lower disease control rate (36.8% vs. 60.9%; p = 0.0145) than those in the Abx (-) group. irAEs were less frequent in the Abx (+) group (29.3% vs. 58.8%; p = 0.0037). The positive impact of irAEs on ICI efficacy was significant in overall population [irAE(-) vs. irAE(+): PFS, 4.4 months (95% CI 2.5-5.3) vs. 8.8 months (95% CI 5.9-13.7); log-rank p = 0.001; Hazard ratio (HR) 1.76, 95% CI 1.14-2.74; p = 0.011; overall survival (OS), 10.6 months (95% CI 7.0-13.1) vs. 18.1 months (95% CI 9.2-25.9); log-rank p = 0.043; HR 1.61, 95% CI 1.01-2.55; p = 0.046] but diminished if received Abx. Notably, the Abx (-)/irAE (+) group had the best outcomes, while the Abx (+)/irAE (-) group had the worst PFS (8.7 vs. 2.4 months; HR 2.07; p = 0.011) and OS (18.1 and 6.8 months; HR 1.89; p = 0.036).
[CONCLUSION] Antibiotic use was linked to reduced ICI efficacy and fewer irAEs, suggesting impaired immune activation in ESCC patients.
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