In:
Oncology, S. Karger AG, Vol. 98, No. 8 ( 2020), p. 534-541
Abstract:
〈 b 〉 〈 i 〉 Introduction: 〈 /i 〉 〈 /b 〉 DNA microarrays, such as the consensus molecular subtype (CMS) classification using & #x3e;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). 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 Here, we validate the 55GC specifically for stage II CC and compare it with CMS categories. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 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. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 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: 〈 i 〉 p 〈 /i 〉 = 0.0049). Multivariate analysis by Cox’s proportional hazard model revealed that the stromal subtype, pT4, and the number of lymph nodes examined ( & #x3c;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 ( 〈 i 〉 p 〈 /i 〉 = 0.0113). 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 We conclude that the 55GC is a useful and reproducible grading system for stage II CC recurrence risk stratification.
Type of Medium:
Online Resource
ISSN:
0030-2414
,
1423-0232
Language:
English
Publisher:
S. Karger AG
Publication Date:
2020
detail.hit.zdb_id:
1483096-6
detail.hit.zdb_id:
250101-6
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