Department of Cancer Center, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Chongqing Clinical Research Center for Geriatrics and Gerontology, Chongqing, China.
Clin Exp Immunol. 2023 Dec 12;214(2):162-169. doi: 10.1093/cei/uxad105.
Chemo-immunotherapy has become the best first-line treatment for advanced lung cancer patients without oncogenic drivers. However, it may also lead to an increased incidence and severity of treatment-related adverse events. In this retrospective study, lung cancer patients administrated with either anti-PD-1 or anti-PD-L1 treatment plus chemotherapy were included. Data on demographic characteristics, disease characteristics, treatment strategies, laboratory results, and clinical outcomes were collected from the Electronic Medical Records System and evaluation scales. Chi-square, univariate, and multivariate logistic regression analyses were used to identify the risk factors for immune-related adverse events (irAEs). A total of 116 patients were included in the study, and the majority experienced treatment-related adverse events. Adverse events of any grade were reported in 114 (98.3%) patients, with 73 (62.9%) experiencing Grade 3 or higher events. The most frequent adverse events were anemia (67.2%), decreased appetite (62.9%), and alopecia (53.4%). Fifty-four (46.6%) patients were diagnosed with irAEs, with hypothyroidism (28.4%) being the most commonly reported. Multivariable analysis demonstrated a significant correlation between the number of treatment cycles, elevated baseline levels of thyroid stimulating hormone (TSH) and interleukin-6 (IL-6) with irAEs (OR = 1.222, P = 0.009, OR = 1.945, P = 0.016, OR = 1.176, P = 0.004), and IL-6 was identified as a strong predictor of severe irAEs (OR = 1.084, P = 0.014). Our study demonstrated the safety of chemo-immunotherapy in lung cancer patients without additional toxicity. The number of treatment cycles, higher baseline levels of TSH and IL-6 were identified as potential clinical biomarkers for irAEs.
化疗免疫治疗已成为无致癌驱动基因的晚期肺癌患者的最佳一线治疗方法。然而,它也可能导致治疗相关不良反应的发生率和严重程度增加。在这项回顾性研究中,纳入了接受抗 PD-1 或抗 PD-L1 治疗加化疗的肺癌患者。从电子病历系统和评估量表中收集人口统计学特征、疾病特征、治疗策略、实验室结果和临床结局的数据。采用卡方检验、单因素和多因素逻辑回归分析来确定免疫相关不良事件(irAEs)的风险因素。本研究共纳入 116 例患者,大多数患者出现治疗相关不良事件。114 例(98.3%)患者报告有任何等级的不良事件,其中 73 例(62.9%)为 3 级或更高级别的事件。最常见的不良事件是贫血(67.2%)、食欲下降(62.9%)和脱发(53.4%)。54 例(46.6%)患者诊断为 irAEs,其中甲状腺功能减退症(28.4%)最常见。多变量分析表明,治疗周期数、基线促甲状腺激素(TSH)和白细胞介素-6(IL-6)水平升高与 irAEs 显著相关(OR=1.222,P=0.009,OR=1.945,P=0.016,OR=1.176,P=0.004),IL-6 是严重 irAEs 的强预测因子(OR=1.084,P=0.014)。我们的研究表明,化疗免疫治疗在肺癌患者中是安全的,没有额外的毒性。治疗周期数、较高的基线 TSH 和 IL-6 水平被确定为 irAEs 的潜在临床生物标志物。