Zhang Zhening, Xie Tong, Qi Changsong, Zhang Xiaotian, Shen Lin, Peng Zhi
Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Cancers (Basel). 2022 Jul 31;14(15):3736. doi: 10.3390/cancers14153736.
Gastrointestinal cancers constitute a major burden of global cancer mortalities. In recent years, the advent of immune checkpoint inhibitors has greatly improved the survival of patients with advanced gastrointestinal cancers, while predictive biomarkers of treatment efficacy and toxicities are still unmet demands.
In our retrospective study, patients with advanced gastrointestinal cancers who received single or double immune checkpoint inhibitors in the Department of Gastrointestinal Oncology in Peking University Cancer Hospital between July 2016 and February 2022 were enrolled. Records of clinicopathological information, survival parameters, safety data, and baseline and posttreatment peripheral blood constituents were retrieved. Cox regression analysis and logistic regression analysis were performed to identify the predictive factors of treatment outcomes and immune-related adverse events.
We demonstrated that early treatment lines, the presence of immune-related adverse events, and a lower C2 neutrophil-to-lymphocyte ratio were independent factors predicting a superior objective response rate and progression-free survival in patients treated with immunotherapy. Lower ECOG PS, higher baseline albumin, and lower C2 neutrophil-to-lymphocyte ratios were independent risk factors for the onset of immune-related adverse events. Patients who succumbed to immune-related adverse events during immunotherapy presented better survival.
Our results indicate that peripheral blood markers have potential for predicting treatment outcomes and immune-related adverse events in patients with advanced gastrointestinal cancer. Prospective validations are warranted.
胃肠道癌症是全球癌症死亡的主要负担。近年来,免疫检查点抑制剂的出现极大地提高了晚期胃肠道癌症患者的生存率,然而治疗疗效和毒性的预测生物标志物仍未得到满足。
在我们的回顾性研究中,纳入了2016年7月至2022年2月期间在北京大学肿瘤医院胃肠肿瘤内科接受单药或双药免疫检查点抑制剂治疗的晚期胃肠道癌症患者。检索临床病理信息、生存参数、安全性数据以及基线和治疗后外周血成分的记录。进行Cox回归分析和逻辑回归分析以确定治疗结果和免疫相关不良事件的预测因素。
我们证明,早期治疗线数、免疫相关不良事件的存在以及较低的C2中性粒细胞与淋巴细胞比值是预测免疫治疗患者具有更高客观缓解率和无进展生存期的独立因素。较低的东部肿瘤协作组体能状态(ECOG PS)、较高的基线白蛋白水平和较低的C2中性粒细胞与淋巴细胞比值是免疫相关不良事件发生的独立危险因素。在免疫治疗期间死于免疫相关不良事件的患者生存情况更好。
我们的结果表明,外周血标志物在预测晚期胃肠道癌症患者的治疗结果和免疫相关不良事件方面具有潜力。需要进行前瞻性验证。