A Validation Study for Recurrence Risk Stratification of Stage II Colon Cancer Using the 55-Gene Classifier.


Journal

Oncology
ISSN: 1423-0232
Titre abrégé: Oncology
Pays: Switzerland
ID NLM: 0135054

Informations de publication

Date de publication:
2020
Historique:
received: 29 01 2020
accepted: 04 02 2020
pubmed: 3 4 2020
medline: 29 8 2020
entrez: 3 4 2020
Statut: ppublish

Résumé

DNA microarrays, such as the consensus molecular subtype (CMS) classification using >600 genes, are used to predict cancer patient prognosis. We recently constructed a simple 55-gene classifier (55GC) system to risk stratify colon cancer (CC). Here, we validate the 55GC specifically for stage II CC and compare it with CMS categories. Tissue sections from 232 stage II CC patients who underwent curative surgery without adjuvant chemotherapy between 2009 and 2012 were subjected to DNA microarray analysis. Based on the 55GC, patients were classified into microsatellite instability-like (27%), chromosomal instability-like (41%), and stromal (32%) subtypes with 5-year relapse-free survival (RFS) rates of 88.5, 83.3, and 71.2%, respectively (stromal vs. others: p = 0.0049). Multivariate analysis by Cox's proportional hazard model revealed that the stromal subtype, pT4, and the number of lymph nodes examined (<12) were independent poor prognostic factors. The overall concordance rate between 55GC and CMS was 72%, and 5-year RFS rates of patients with CMS1, CMS2, CMS3, and CMS4 cancers were 100, 85.5, 92.3, and 73.0%, respectively (p = 0.0113). We conclude that the 55GC is a useful and reproducible grading system for stage II CC recurrence risk stratification.

Identifiants

pubmed: 32235113
pii: 000506369
doi: 10.1159/000506369
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

534-541

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Eiji Shinto (E)

Department of Surgery, National Defense Medical College, Tokorozawa, Japan, shinto@ndmc.ac.jp.

Eiji Oki (E)

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Mototsugu Shimokawa (M)

Clinical Research Institute, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

Shigeki Yamaguchi (S)

Department of Gastroenterological Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.

Megumi Ishiguro (M)

Department of Translational Oncology, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University, Tokyo, Japan.

Masaru Morita (M)

Gastroenterological Surgery, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

Tetsuya Kusumoto (T)

Department of Gastroenterological Surgery, Clinical Research Center, Cancer Research Division, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.

Naohiro Tomita (N)

Department of Surgery, Hyogo College of Medicine, Nishinomiya, Japan.

Yojiro Hashiguchi (Y)

Department of Surgery, Teikyo University School of Medicine, Tokyo, Japan.

Masafumi Tanaka (M)

Coloproctology Center, Takano Hospital, Kumamoto, Japan.

Shinobu Ohnuma (S)

Department of Surgery, Tohoku University Hospital, Sendai, Japan.

Sachiyo Tada (S)

LS Business, Sysmex Corporation, Kobe, Japan.

Tomoko Matsushima (T)

LS Business, Sysmex Corporation, Kobe, Japan.

Kazuo Hase (K)

Department of Surgery, National Defense Medical College, Tokorozawa, Japan.

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