Huang Yuan-Heng, Yang Guo-Zhen, Chen Hui-Guo, Li Xiao-Jun, Wu Yong-Hui, Zhang Kai, Xu Jian-Nan, Zhang Jian
Department of Cardiothoracic Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Guangzhou 510060, Guangdong Province, China.
World J Gastrointest Oncol. 2024 Sep 15;16(9):3887-3897. doi: 10.4251/wjgo.v16.i9.3887.
Immunochemotherapy involving the combination of programmed cell death 1/programmed cell death ligand 1 inhibitors with chemotherapy has advanced the treatment of locally advanced esophageal squamous cell carcinoma (ESCC). The use of corticosteroids as pretreatment might reduce immunotherapy efficacy.
To investigate the impact of baseline corticosteroid use on neoadjuvant immunochemotherapy (nIC) outcomes in locally advanced ESCC patients.
Patients with locally advanced ESCC who received nIC at Sun Yat-sen University Cancer Center and the Third Affiliated Hospital of Sun Yat-sen University were included. Patients were divided into dexamethasone and antihistamine groups on the basis of the administered pretreatment. Antiallergic efficacy and safety were evaluated, as well as its impact on short-term efficacy [complete pathological response (pCR), major pathological response (MPR)] and long-term efficacy [overall survival (OS), progression-free survival (PFS)] of nIC.
From September 2019 to September 2023, 142 patients were analyzed. No severe treatment-related adverse events or deaths were observed. Allergy occurrence was greater in the antihistamine group ( = 0.014). Short-term efficacy was not significantly different: The pCR rates were 29.9% and 40.0%, and the MPR rates were 57.9% and 65.7% in the dexamethasone and antihistamine groups, respectively. The long-term efficacy was not significantly different: The 2 years OS rates were 95.2% and 93.5%, and the 2 years PFS rates were 90.3% and 87.8%. Subgroup analysis revealed no difference in OS between the 20 mg dexamethasone group and the < 20 mg dexamethasone group, but PFS was significantly greater in the 20 mg dexamethasone group (93.9% 56.4%, = 0.001).
Dexamethasone or antihistamines can be used before nIC in locally advanced ESCC without affecting short- or long-term efficacy. Administering 20 mg dexamethasone before nIC may improve PFS in ESCC.
程序性细胞死亡蛋白1/程序性细胞死亡配体1抑制剂与化疗联合的免疫化疗推动了局部晚期食管鳞状细胞癌(ESCC)的治疗进展。使用皮质类固醇作为预处理可能会降低免疫治疗效果。
探讨基线使用皮质类固醇对局部晚期ESCC患者新辅助免疫化疗(nIC)疗效的影响。
纳入在中山大学肿瘤防治中心和中山大学附属第三医院接受nIC治疗的局部晚期ESCC患者。根据所给予的预处理将患者分为地塞米松组和抗组胺药组。评估抗过敏疗效和安全性,以及其对nIC短期疗效[完全病理缓解(pCR)、主要病理缓解(MPR)]和长期疗效[总生存期(OS)、无进展生存期(PFS)]的影响。
2019年9月至2023年9月,对142例患者进行了分析。未观察到严重的治疗相关不良事件或死亡。抗组胺药组过敏发生率更高(P = 0.014)。短期疗效无显著差异:地塞米松组和抗组胺药组的pCR率分别为29.9%和40.0%,MPR率分别为57.9%和65.7%。长期疗效无显著差异:两年OS率分别为95.2%和93.5%,两年PFS率分别为90.3%和87.8%。亚组分析显示,20 mg地塞米松组与<20 mg地塞米松组的OS无差异,但20 mg地塞米松组的PFS显著更高(93.9%对56.4%,P = 0.001)。
地塞米松或抗组胺药可在局部晚期ESCC的nIC前使用,而不影响短期或长期疗效。nIC前给予20 mg地塞米松可能会改善ESCC的PFS。