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胃癌患者辅助化疗后 TIL(肿瘤浸润淋巴细胞)与生存:CLASSIC 试验的事后分析

英文原题:Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial.

查看英文原题

Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial.

PubMed 2023/04/07(内容时间) Br J Cancer Q1 · IF 7.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

这是首项提出在常规 HE 染色组织切片中自动量化的 TIL 密度可作为识别从辅助化疗中获益的 II-III 期胃癌患者的新型、有临床实用价值的生物标志物的研究。

中文摘要

仅部分II至III期胃癌患者能从术后辅助化疗获益。单位面积TIL(肿瘤浸润淋巴细胞)密度被认为是潜在获益预测标志物。

使用深度学习分析HE数字切片,量化延世癌症中心307例胃癌(193例手术加辅助化疗,114例单纯手术)及CLASSIC试验629例胃癌(325例手术加化疗,304例单纯手术)的TIL密度,并分析其与无病生存期(DFS)及临床病理变量的关系。

在延世中心和CLASSIC队列中,单纯手术患者里TIL高密度者DFS均长于低密度者(p分别为0.007和0.013)。此外,CLASSIC试验TIL低密度患者接受手术加化疗较单纯手术DFS更长(p=0.003)。TIL密度与其他临床病理变量无显著关系。

这是首项提示可在常规HE切片中自动量化TIL密度,并将其作为临床实用新标志物识别II至III期辅助化疗获益胃癌患者的研究。仍需前瞻性研究验证。

展开英文摘要原文

Only a subset of gastric cancer (GC) patients with stage II-III benefits from chemotherapy after surgery. Tumour infiltrating lymphocytes per area (TIL density) has been suggested as a potential predictive biomarker of chemotherapy benefit.

We quantified TIL density in digital images of haematoxylin-eosin (HE) stained tissue using deep learning in 307 GC patients of the Yonsei Cancer Center (YCC) (193 surgery+adjuvant chemotherapy [S + C], 114 surgery alone [S]) and 629 CLASSIC trial GC patients (325 S + C and 304 S). The relationship between TIL density, disease-free survival (DFS) and clinicopathological variables was analysed.

YCC S patients and CLASSIC S patients with high TIL density had longer DFS than S patients with low TIL density (P = 0.007 and P = 0.013, respectively). Furthermore, CLASSIC patients with low TIL density had longer DFS if treated with S + C compared to S (P = 0.003). No significant relationship of TIL density with other clinicopathological variables was found.

This is the first study to suggest TIL density automatically quantified in routine HE stained tissue sections as a novel, clinically useful biomarker to identify stage II-III GC patients deriving benefit from adjuvant chemotherapy. Validation of our results in a prospective study is warranted.

论文信息

作者
Liu DHW、Kim YW、Sefcovicova N、Laye JP、Hewitt LC、Irvine AF、Vromen V、Janssen Y
第一作者单位
Department of Pathology, GROW School for Oncology and Reproduction, Maastricht University Medical Center+, Maastricht, The Netherlands.Netherlands
通讯作者单位
Department of Pathology, GROW School for Oncology and Reproduction, Maastricht University Medical Center+, Maastricht, The Netherlands. h.grabsch@maastrichtuniversity.nl.Netherlands
文献类型
临床试验 · 非美国政府资助研究
期刊
British journal of cancer2023 Jun
原文标识
PubMed 37029200 · DOI 10.1038/s41416-023-02257-3