CDX2 prognostic value in stage II/III resected colon cancer is related to CMS classification

被引:51
作者
Pilati, C. [1 ]
Taieb, J. [2 ]
Balogoun, R. [1 ]
Marisa, L. [3 ]
de Reynies, A. [3 ]
Laurent-Puig, P. [1 ]
机构
[1] Univ Paris 05, INSERM, UMR S1147, Personalized Med,Pharmacogen,Therapeut Optimizat, 45 Rue St Peres, F-75006 Paris, France
[2] Univ Paris 05, Georges Pompidou Hosp, AP HP, Dept Hepatogastroenterol & Gastrointestinal Oncol, Paris, France
[3] Ligue Natl Canc, Programme Cartes Identite Tumeurs CIT, Paris, France
关键词
colon cancer; CDX2; consensus molecular subtype classification (CMS); COLORECTAL-CANCER; TGF-BETA; MICROSATELLITE INSTABILITY; MOLECULAR SUBTYPES; EXPRESSION; PHENOTYPE; FEATURES; SYSTEM; TUMORS;
D O I
10.1093/annonc/mdx066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Caudal-type homeobox transcription factor 2 (CDX2) is involved in colon cancer (CC) oncogenesis and has been proposed as a prognostic biomarker in patients with stage II or III CC. Patients and methods: We analyzed CDX2 expression in a series of 469 CC typed for the new international consensus molecular subtype (CMS) classification, and we confirmed results in a series of 90 CC. Results: Here, we show that lack of CDX2 expression is only present in the mesenchymal subgroup (CMS4) and in MSI-immune tumors (CMS1) and not in CMS2 and CMS3 colon cancer. Although CDX2 expression was a globally independent prognostic factor, loss of CDX2 expression is not associated with a worse prognosis in the CMS1 group, but is highly prognostic in CMS4 patients for both relapse free and overall survival. Similarly, lack of CDX2 expression was a bad prognostic factor in MSS patients, but not in MSI. Conclusions: Our work suggests that combination of the consensual CMS classification and lack of CDX2 expression could be a useful marker to identify CMS4/CDX2-negative patients with a very poor prognosis.
引用
收藏
页码:1032 / 1035
页数:4
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