间皮素作为癌症免疫治疗的生物标志物和治疗靶点
Mesothelin as Biomarker and Therapeutic Target for Immunotherapy in Cancer.
癌症仍是一个关键的全球健康问题,原因在于发现晚、耐药和高死亡率。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial.
Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial.
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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。
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。
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.
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