Claudin 18.2 靶向:泛癌视角
Claudin 18.2 Targeting: A Pan-Cancer Perspective.
FDA 对 zolbetuximab 批准的 CLDN18.2 阈值为 ≥ 75% 中度至强染色。
英文原题:Expression of programmed cell death protein 1 (PD-1) and programmed cell death 1 ligand (PD-L1) in adenocarcinomas of the gastroesophageal junction change significantly after neoadjuvant treatment.
在本研究中,我们能够显示,在接受新辅助化疗后,胃食管交界处腺癌患者的肿瘤细胞PD-1和PD-L1表达显著改变。基于这些观察,患者可能从细胞毒性化疗与PD-1轴阻断的联合使用中获益。
细胞毒性化疗对癌细胞及瘤周细胞中程序性细胞死亡1(PD-1)及其配体(PD-L1)表达的影响尚不明确。本研究旨在探讨新辅助化疗对胃食管结合部腺癌中PD-1和PD-L1表达的影响。
PD-1和PD-L1在癌 cells 和TIL(肿瘤浸润淋巴细胞)中的表达,在来自接受过预处理和根治性切除的胃食管交界处腺癌患者的配对诊断活检和手术标本中,通过免疫组织化学进行了评估。
40例患者有配对的肿瘤样本。新辅助治疗后,癌细胞中PD-1表达(p < 0.001;精确对称检验)和TIL(肿瘤浸润淋巴细胞)中PD-1表达(p < 0.001;精确对称检验)显著增加。此外,我们观察到新辅助治疗后癌细胞中PD-L1表达显著降低(p = 0.003)。
BACKGROUND: The effects of cytotoxic chemotherapy on the expression of programmed cell death 1 (PD-1) and its ligand (PD-L1) in cancer cells and peritumoral cells are unclear. The aim of this study was to investigate the impact of neoadjuvant chemotherapy on PD-1 and PD-L1 expression in adenocarcinomas of the gastroesophageal junction. METHODS: PD-1 and PD-L1 expression in cancer cells and tumor-infiltrating lymphocytes in paired diagnostic biopsies and surgical specimens from patients with pretreated and curatively resected adenocarcinomas of the gastroesophageal junction were evaluated by immunohistochemistry. RESULTS: Paired tumor samples were available from 40 patients. PD-1 expression in cancer cells (p < 0.001; Exact Symmetry Test) and tumor-infiltrating lymphocytes (p < 0.001; Exact Symmetry Test) increased significantly after neoadjuvant therapy. Furthermore, we observed a significant decrease in PD-L1 expression in cancer cells (p = 0.003) after neoadjuvant therapy was observed. CONCLUSION: In this study we could show that tumor-cell expression of PD-1 and PD-L1 was significantly altered in patients with adenocarcinomas of the gastroesophageal junction after receiving neoadjuvant chemotherapy. Based on these observations, patients might profit from the combined use of cytotoxic chemotherapy and the blockade of the PD-1 axis.
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