纵向血浆代谢组学指导食管鳞状细胞癌化疗免疫治疗的动态风险评估与饮食调节
Longitudinal Plasma Metabolomics Guides Dynamic Risk Assessment and Dietary Modulation for Esophageal Squamous Cell Cancer Chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Case of Complete Response to ICI Therapy for Unresectable Esophageal Squamous Cell Carcinoma.
A Case of Complete Response to ICI Therapy for Unresectable Esophageal Squamous Cell Carcinoma.
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与既往报道认为高 Treg 浸润与 ICI 疗效降低相关相反,我们的患者表现出异常长期的 CR。潜在影响因素包括化疗的协同作用、Treg 功能改变以及肿瘤相关巨噬细胞极少。本病例凸显了肿瘤微环境相互作用的复杂性,并提示需进一步研究 Treg 生物学在预测 ESCC 中 ICI 治疗结局方面的作用。
免疫检查点抑制剂(ICIs)联合化疗是不可切除晚期食管鳞状细胞癌(ESCC)的标准一线治疗。已知TIL(肿瘤浸润淋巴细胞)(TILs)影响ICIs的疗效;然而,调节性T细胞(Tregs)的作用仍不清楚。我们报告一例罕见病例,尽管存在大量Treg浸润,但化疗-免疫治疗仍实现了长期完全缓解(CR)。病例报告:一名49岁女性被诊断为临床IVA期ESCC,接受帕博利珠单抗联合FP(5-氟尿嘧啶和顺铂)化疗。四个周期后,通过内镜、活检、计算机断层扫描(CT)和正电子发射断层扫描-CT(PET-CT)确认完全缓解。帕博利珠单抗单药治疗维持CR达24个月,之后出现疾病进展,此后以紫杉醇成功治疗。治疗前活检免疫组织化学显示大量FoxP3阳性Treg浸润、CD8阳性细胞毒性T淋巴细胞有限、PD-L1缺失、肿瘤相关巨噬细胞极少,以及HLA I类分子高表达。
BACKGROUND/AIM: Immune checkpoint inhibitors (ICIs) combined with chemotherapy are standard first-line therapy for unresectable advanced esophageal squamous cell carcinoma (ESCC). Tumor-infiltrating lymphocytes (TILs) are known to influence the efficacy of ICIs; however, the role of regulatory T cells (Tregs) remains unclear. We report a rare case in which long-term complete response (CR) to chemo-immunotherapy was achieved despite abundant Treg infiltration. CASE REPORT: A 49-year-old woman diagnosed with clinical stage IVA ESCC received pembrolizumab combined with FP (5-fluorouracil and cisplatin) chemotherapy. After four cycles, a complete response was confirmed by endoscopy, biopsy, computed tomography (CT), and positron emission tomography-CT (PET-CT). Pembrolizumab monotherapy maintained CR for 24 months before disease progression occurred, treated successfully thereafter with paclitaxel. Pretreatment biopsy immunohistochemistry revealed abundant FoxP3-positive Treg infiltration, limited CD8-positive cytotoxic T lymphocytes, absence of PD-L1, minimal tumor-associated macrophages, and high expression of HLA class I molecules. CONCLUSION: Contrary to previous reports that associated high Treg infiltration with reduced efficacy of ICIs, our patient demonstrated exceptional long-term CR. Potential influencing factors include synergistic chemotherapy effects, altered Treg function, and minimal presence of tumor-associated macrophages. This case underscores the complexity of tumor microenvironment interactions and suggests further investigation into Treg biology in predicting ICI treatment outcomes in ESCC.
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