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恶病质的纵向变化对免疫检查点抑制剂治疗食管鳞癌(ESCC)患者疗效和毒性的影响。

Effect of longitudinal changes of cachexia on the efficacy and toxicity of immune checkpoint inhibitors in esophageal squamous cell cancer (ESCC) patients.

机构信息

Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.

Department of Portal Hypertension, Shandong Public Health Clinical Center, Shandong University, Jinan, China.

出版信息

Nutrition. 2024 Aug;124:112462. doi: 10.1016/j.nut.2024.112462. Epub 2024 Apr 5.

Abstract

PURPOSE

Immune checkpoint inhibitors (ICIs) have enhanced survival in advanced esophageal squamous cell cancer (ESCC) patients, but their efficacy varies. Cachexia, characterized by muscle loss and significant weight loss, might influence ICI response. This study examines the relationship between cachexia's longitudinal changes and ICI outcomes in ESCC patients.

METHODS

ESCC patients undergoing at least two ICI cycles from 2017 to 2021 were studied. Cachexia's baseline and evolving patterns during ICI treatment were observed. Kaplan-Meier and Cox regression analyses were used to assess cachexia's effect on ICI efficacy. Chi-square tests were used to determine cachexia's link to immune-related adverse effects (irAEs).

RESULTS

Two hundred seventy-eight ICI-treated patients had a median progression-free survival (PFS) of 5.78 months and overall survival (OS) of 8.3 months. Pretreatment cachexia led to worse outcomes: PFS 7.87 versus 5.3 months, time to progression (TTP) 10.9 versus 6.1 months, and OS 14.3 versus 9.2 months. Irreversible cachexia showed the poorest results. Cachexia's changes weren't associated with irAEs.

CONCLUSION

Baseline and evolving cachexia significantly impact ICI efficacy in ESCC patients. Continuous cachexia monitoring during ICI therapy is crucial for optimal ESCC management.

摘要

目的

免疫检查点抑制剂 (ICI) 提高了晚期食管鳞状细胞癌 (ESCC) 患者的生存率,但疗效存在差异。恶病质表现为肌肉减少和明显体重下降,可能影响 ICI 反应。本研究探讨了 ESCC 患者恶病质的纵向变化与 ICI 结果之间的关系。

方法

研究了 2017 年至 2021 年期间至少接受两个 ICI 周期治疗的 ESCC 患者。观察了 ICI 治疗期间恶病质的基线和演变模式。使用 Kaplan-Meier 和 Cox 回归分析评估恶病质对 ICI 疗效的影响。使用卡方检验确定恶病质与免疫相关不良事件 (irAEs) 的关系。

结果

278 名接受 ICI 治疗的患者中位无进展生存期 (PFS) 为 5.78 个月,总生存期 (OS) 为 8.3 个月。治疗前恶病质导致更差的结局:PFS 7.87 与 5.3 个月,进展时间 (TTP) 10.9 与 6.1 个月,OS 14.3 与 9.2 个月。不可逆恶病质的结果最差。恶病质的变化与 irAEs 无关。

结论

基线和演变中的恶病质显著影响 ESCC 患者的 ICI 疗效。在 ICI 治疗期间持续监测恶病质对于 ESCC 的最佳管理至关重要。

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