Risk factors for lymph node metastasis in patients with pT2 colon cancer in Denmark from 2016 to 2019-A nationwide cohort study

被引:5
作者
Hartwig, Morten [1 ,4 ]
Rosen, Andreas [1 ]
Vogelsang, Rasmus [1 ]
Fiehn, Anne-Marie [1 ,2 ,3 ]
Gogenur, Ismail [1 ,3 ]
机构
[1] Zealand Univ Hosp Koege, Ctr Surg Sci, Dept Surg, Koege, Denmark
[2] Zealand Univ Hosp, Dept Pathol, Roskilde, Denmark
[3] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[4] Zealand Univ Hosp Koege, Ctr Surg Sci, Dept Surg, Lykkebaekvej 1, DK-4600 Koege, Denmark
关键词
colon cancer; histological risk factors; lymph node metastases; T2; category; COLORECTAL-CANCER; CARCINOMA; T1; INVASION;
D O I
10.1111/codi.16469
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimThe majority of patients with pT2 colon cancer have no lymph node metastasis (LNM). Knowledge of risk factors for LNM in pT2 colon cancer could identify patients at low risk and thereby potential candidates for local tumour excision. The aim of this work was to identify risk factors for LNM in pT2 colon cancer and describe a subgroup of low-risk patients. MethodThis is a retrospective cohort study of patients with pT2 colon cancer from a nationwide Danish colorectal cancer database. Age, tumour size, location, histological type, mismatch repair protein status and venous, lymphatic and perineural invasion were included as potential risk factors in multivariate analysis. The primary outcome was LNM. ResultsWe identified 1306 patients with pT2 colon cancer. LNM was present in 244 (19%). Demographic data were comparable in patients with and without LNM, and 864 patients who had complete histological data were included for multivariate analysis. Lymphatic (OR = 3.60, 95% CI 2.14-5.9), venous (OR = 1.70, 95% CI 1.03-2.74) and perineural (OR = 4.61, 95% CI 1.60-13.5) invasion were independent risk factors for LNM. Patients with deficient mismatch repair protein tumours had a decreased risk of LNM (OR = 0.55, 95% CI 0.31-0.95). Patients with clinical Stage I colon cancer and without risk factors had a 10.5% (47/443) risk of LNM. For patients with tumours with deficient mismatch repair protein status and no risk factors, the risk was 7.9%. ConclusionLymphatic, venous and perineural invasion are significant risk factors for LNM, and we identified a subgroup of patients with a low risk of LNM.
引用
收藏
页码:872 / 879
页数:8
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