Shi Yuequan, Liu Xiaoyan, Du Juan, Zhang Dongming, Liu Jia, Chen Minjiang, Zhao Jing, Zhong Wei, Xu Yan, Wang Mengzhao
Department of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Department of Clinical Laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Thorac Cancer. 2022 Jan;13(2):219-227. doi: 10.1111/1759-7714.14248. Epub 2021 Nov 25.
Pretreatment and on-treatment plasma cytokine levels in predicting clinical benefit in patients with advanced non-small cell lung cancer (NSCLC) treated with anti-programmed death-1 (PD-1)-based chemotherapy is still a matter of debate.
We measured 12 kind of plasma cytokines in patients with stage III/IV NSCLC before and during treatment with anti-PD-1 based chemotherapy. Associations with best overall response, and survival including progression-free survival (PFS) and overall survival (OS) were assessed using Chi-square test and Kaplan-Meier plots with log-rank test, respectively. Logistic regression and Cox regression were used to determine independent risk factors.
Of a total of 60 patients, high-level of pretreatment interleukin-2 was associated with longer PFS (log rank p = 0.049), while high-level of pretreatment interleukin-8 was associated with shorter OS (log rank p = 0.006). Increased on-treatment interleukin-1β (IL-1β) was associated with both better response (odds ratio [OR] 6.233, 95% confidential interval [CI]: 1.451-26.344, p = 0.013) and longer PFS (hazard ratio [HR] 0.305, 95% CI: 0.127-0.730, p = 0.008). On the contrary, increased on-treatment interleukin-6 (IL-6) was associated with a worse response (OR 0.015, 95% CI: 0.001-0.400, p = 0.012), worse PFS (HR 2.639, 95% CI: 1.163-5.991, p = 0.020) and worse OS (HR 2.742, 95% CI: 1.063-7.074, p = 0.037). Increased interferon-γ (IFN-γ) was found to be associated with better PFS (HR 0.336, 95% CI: 0.153-0.745, p = 0.007).
In patients with advanced NSCLC who received chemoimmunotherapy, on-treatment increased IL-1β and IFN-γ may serve as positive indicator of efficacy, while on-treatment increased IL-6 might play a predictive role of worse clinical outcome.
在接受基于抗程序性死亡蛋白 1(PD-1)化疗的晚期非小细胞肺癌(NSCLC)患者中,治疗前和治疗期间血浆细胞因子水平对预测临床获益仍存在争议。
我们在 III/IV 期 NSCLC 患者接受基于抗 PD-1 化疗的治疗前和治疗期间测量了 12 种血浆细胞因子。分别使用卡方检验和带有对数秩检验的 Kaplan-Meier 曲线评估与最佳总体缓解以及生存(包括无进展生存期(PFS)和总生存期(OS))的相关性。使用逻辑回归和 Cox 回归确定独立危险因素。
在总共 60 例患者中,治疗前白细胞介素-2 水平高与较长的 PFS 相关(对数秩 p = 0.049),而治疗前白细胞介素-8 水平高与较短的 OS 相关(对数秩 p = 0.006)。治疗期间白细胞介素-1β(IL-1β)升高与更好的缓解相关(优势比[OR]6.233,95%置信区间[CI]:1.451 - 26.344,p = 0.013)以及较长的 PFS 相关(风险比[HR]0.305,95%CI:0.127 - 0.730,p = 0.008)。相反,治疗期间白细胞介素-6(IL-6)升高与更差的缓解相关(OR 0.015,95%CI:0.001 - 0.400,p = 0.012)、更差的 PFS(HR 2.639,95%CI:1.163 - 5.991,p = 0.020)和更差的 OS(HR 2.742,95%CI:1.063 - 7.074,p = 0.037)。发现干扰素-γ(IFN-γ)升高与更好的 PFS 相关(HR 0.336,95%CI:0.153 - 0.745,p = 0.007)。
在接受化疗免疫治疗的晚期 NSCLC 患者中,治疗期间升高的 IL-1β 和 IFN-γ 可能作为疗效的阳性指标,而治疗期间升高的 IL-6 可能对更差的临床结局起预测作用。