He Jinxian, Liang Gaofeng, Yu Hongyan, Shen Weiyu, Pimiento Jose M, Anker Christopher J, Koyanagi Kazuo, Liu Jiacong, Hu Jian
Department of Thoracic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Thoracic Surgery, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
J Thorac Dis. 2024 Oct 31;16(10):6999-7015. doi: 10.21037/jtd-24-1365. Epub 2024 Oct 28.
There is currently no consensus on whether intensive cycles of neoadjuvant immunochemotherapy provide greater benefit than do less intensive cycles (two cycles) in esophageal cancer (EC). Therefore, in this study, we assessed the efficacy and safety of three to four cycles of neoadjuvant immunochemotherapy compared to two cycles for treating patients with locally advanced esophageal squamous cell carcinoma (ESCC).
This is a retrospective study of patients enrolled on previous clinical studies involving locally/regionally advanced ESCC (St. II-IVA) who received preoperative immunochemotherapy at the Department of Thoracic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine from 2019 to 2021. In this study, patients were planned to receive 2-4 cycles of chemoimmunotherapy. In this secondary analysis, patients who received three to four cycles of neoadjuvant immunochemotherapy were compared to those receiving two cycles in terms of safety and oncologic outcomes. The follow-up duration required for inclusion was at least one year following surgery, or until the patient died or independently elected to cease treatment if less than one year.
Our study identified a total of 142 participants, who were categorized into two groups based on the number of neoadjuvant treatment cycles: the two cycles group (2 cycles) (n=65) and the three to four cycles group (3-4 cycles) (n=77). Regarding the rate of major pathologic response (MPR), the rates for the 3-4 cycles and 2 cycles groups were 22.1% and 20.0%, respectively, although this difference was not statistically significant (P=0.25). Similarly, the rate of pathologic complete remission (pCR) was higher in the 3-4 cycles group at 14.3% compared to 7.7% in the 2 cycles group, but the difference did not reach statistical significance (P=0.07). However, the incidence of adverse events (AEs) classified as grade 3 or 4 was significantly higher in the 3-4 cycles group than in the 2 cycles group (36.4% 18.5%; P=0.02). The median disease-free survival (DFS) for the 3-4 cycles group was 30.8 months [95% confidence interval (CI): not reached to not reached] and was not reached in the 2 cycles group (hazard ratio 2.35, 95% CI: 1.134-4.86; P=0.02). The 2 cycles group did not reach the median overall survival (OS) (hazard ratio 2.47, 95% CI: 1.08-5.53; P=0.045), with that in the 3-4 cycles group 34.9 months (95% CI: 24.5 to not reached). Interestingly, the survival outcomes were more favorable in the 2 cycles group for certain subgroups of patients: those who were male, those with a history of smoking, those with a history of drinking, and those who did not achieve MPR.
Two cycles of neoadjuvant immunochemotherapy can be considered in locally advanced ESCC at high risk of developing toxicity with 3-4 cycles with similar oncologic outcomes.
目前对于新辅助免疫化疗的强化疗程(三个周期以上)相比非强化疗程(两个周期)在食管癌(EC)治疗中是否能带来更大获益尚无定论。因此,在本研究中,我们评估了三至四个周期新辅助免疫化疗与两个周期新辅助免疫化疗相比,治疗局部晚期食管鳞状细胞癌(ESCC)患者的疗效和安全性。
这是一项对参与既往临床研究的患者的回顾性研究,这些患者患有局部/区域晚期ESCC(II-IVA期),于2019年至2021年在浙江大学医学院附属第一医院胸外科接受术前免疫化疗。在本研究中,患者计划接受2-4个周期的化疗免疫治疗。在这项二次分析中,将接受三至四个周期新辅助免疫化疗的患者与接受两个周期新辅助免疫化疗的患者在安全性和肿瘤学结局方面进行比较。纳入所需的随访时间为术后至少一年,或如果少于一年则直至患者死亡或自主选择停止治疗。
我们的研究共纳入142名参与者,根据新辅助治疗周期数分为两组:两个周期组(2个周期)(n=65)和三至四个周期组(3-4个周期)(n=77)。关于主要病理缓解(MPR)率,3-4个周期组和2个周期组的MPR率分别为22.1%和20.0%,尽管这一差异无统计学意义(P=0.25)。同样,病理完全缓解(pCR)率在3-4个周期组中更高,为14.3%,而2个周期组为7.7%,但差异未达到统计学意义(P=0.07)。然而,3-4个周期组中3级或4级不良事件(AE)的发生率显著高于2个周期组(36.4%对18.5%;P=0.02)。3-4个周期组的中位无病生存期(DFS)为30.8个月[95%置信区间(CI):未达到至未达到],2个周期组未达到(风险比2.35,95%CI:1.134-4.86;P=0.02)。2个周期组未达到中位总生存期(OS)(风险比2.47,95%CI:1.08-5.53;P=0.045),3-4个周期组的OS为34.9个月(95%CI:24.5至未达到)。有趣的是,对于某些亚组患者,2个周期组的生存结局更有利:男性、有吸烟史、有饮酒史以及未达到MPR的患者。
对于局部晚期ESCC且使用三至四个周期有发生毒性高风险的患者,可考虑采用两个周期的新辅助免疫化疗,其肿瘤学结局相似。