Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital, 1 Gustave L. Levy Place, New York, NY 10029, USA.
Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, 281 1st Ave, New York, NY 10003, USA.
Immunotherapy. 2024;16(12):829-840. doi: 10.1080/1750743X.2024.2379230. Epub 2024 Aug 19.
Tumor-promoting inflammation and inflammatory cytokines are linked to immune checkpoint blockade (ICB) resistance. We assessed the associations between pre-treatment Interleukin-6 (IL-6), Interleukin-8 (IL-8) levels and on-treatment changes in IL-6, IL-8 and C-reactive protein (CRP) with ICB trial end points. 27 studies representing 6,719 patients were included. Low pre-treatment IL-6 levels were associated with improved objective response rate (ORR) (odds ratio (OR) = 0.31 [0.18-0.55]) and better progression-free survival (PFS) (hazard ratio (HR) = 0.59 [0.48-0.72]) and overall survival (OS) [95% confidence interval (CI)] (HR = 0.42 [0.35-0.50]). Low pre-treatment IL-8 levels were associated with improved ORR (OR = 0.47 [0.36-0.61]) and better PFS (HR = 0.65 [0.58-0.74]) and OS (HR = 0.44 [0.39-0.51]). On-treatment decline in CRP was associated with improved ORR (OR = 0.18 [0.11-0.20]), PFS (HR = 0.40 [0.31-0.91]) and OS (HR = 0.48 [0.40-0.58]). Peripheral blood cytokines warrant further evaluation as enrichment and pharmacodynamic biomarkers for strategies targeting tumor-promoting inflammation.
促瘤炎症和炎症细胞因子与免疫检查点阻断(ICB)耐药有关。我们评估了治疗前白细胞介素-6(IL-6)、白细胞介素-8(IL-8)水平以及治疗过程中 IL-6、IL-8 和 C 反应蛋白(CRP)的变化与 ICB 试验终点的关系。共纳入了 27 项研究,代表了 6719 例患者。低治疗前 IL-6 水平与提高客观缓解率(ORR)(优势比(OR)=0.31 [0.18-0.55])和改善无进展生存期(PFS)(风险比(HR)=0.59 [0.48-0.72])和总生存期(OS)[95%置信区间(CI)](HR=0.42 [0.35-0.50])有关。低治疗前 IL-8 水平与提高 ORR(OR=0.47 [0.36-0.61])和改善 PFS(HR=0.65 [0.58-0.74])和 OS(HR=0.44 [0.39-0.51])有关。CRP 治疗期间的下降与提高 ORR(OR=0.18 [0.11-0.20])、PFS(HR=0.40 [0.31-0.91])和 OS(HR=0.48 [0.40-0.58])有关。外周血细胞因子作为针对促瘤炎症的策略的富集和药效学生物标志物值得进一步评估。