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Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial
DC Field | Value | Language |
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dc.contributor.author | 김현기 | - |
dc.contributor.author | 정재호 | - |
dc.date.accessioned | 2024-05-30T07:06:03Z | - |
dc.date.available | 2024-05-30T07:06:03Z | - |
dc.date.issued | 2023-06 | - |
dc.identifier.issn | 0007-0920 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/199550 | - |
dc.description.abstract | BackgroundOnly 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.MethodsWe 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.ResultsYCC 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.ConclusionThis 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. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Nature Publishing Group on behalf of Cancer Research UK | - |
dc.relation.isPartOf | BRITISH JOURNAL OF CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Biomarkers | - |
dc.subject.MESH | Chemotherapy, Adjuvant | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lymphocytes, Tumor-Infiltrating* / pathology | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Stomach Neoplasms* / drug therapy | - |
dc.subject.MESH | Stomach Neoplasms* / surgery | - |
dc.title | Tumour infiltrating lymphocytes and survival after adjuvant chemotherapy in patients with gastric cancer: post-hoc analysis of the CLASSIC trial | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pathology (병리학교실) | - |
dc.contributor.googleauthor | Drolaiz H W Liu | - |
dc.contributor.googleauthor | Young-Woo Kim | - |
dc.contributor.googleauthor | Nina Sefcovicova | - |
dc.contributor.googleauthor | Jon P Laye | - |
dc.contributor.googleauthor | Lindsay C Hewitt | - |
dc.contributor.googleauthor | Andrew F Irvine | - |
dc.contributor.googleauthor | Vincent Vromen | - |
dc.contributor.googleauthor | Yannick Janssen | - |
dc.contributor.googleauthor | Naser Davarzani | - |
dc.contributor.googleauthor | Gregorio E Fazzi | - |
dc.contributor.googleauthor | Shahab Jolani | - |
dc.contributor.googleauthor | Veerle Melotte | - |
dc.contributor.googleauthor | Derek R Magee | - |
dc.contributor.googleauthor | Myeong-Cherl Kook | - |
dc.contributor.googleauthor | Hyunki Kim | - |
dc.contributor.googleauthor | Rupert Langer | - |
dc.contributor.googleauthor | Jae-Ho Cheong | - |
dc.contributor.googleauthor | Heike I Grabsch | - |
dc.identifier.doi | 10.1038/s41416-023-02257-3 | - |
dc.contributor.localId | A01108 | - |
dc.contributor.localId | A03717 | - |
dc.relation.journalcode | J00406 | - |
dc.identifier.eissn | 1532-1827 | - |
dc.identifier.pmid | 37029200 | - |
dc.contributor.alternativeName | Kim, Hyunki | - |
dc.contributor.affiliatedAuthor | 김현기 | - |
dc.contributor.affiliatedAuthor | 정재호 | - |
dc.citation.volume | 128 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 2318 | - |
dc.citation.endPage | 2325 | - |
dc.identifier.bibliographicCitation | BRITISH JOURNAL OF CANCER, Vol.128(12) : 2318-2325, 2023-06 | - |
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