Department of Surgery, University of Iowa Hospitals & Clinics, Iowa City, IA, USA.
Holden Comprehensive Cancer Center Biostatistics Core, University of Iowa, Iowa City, IA, USA.
J Gastrointest Surg. 2020 Jun;24(6):1402-1410. doi: 10.1007/s11605-020-04543-4. Epub 2020 Mar 3.
Approximately 40% of colorectal cancers have a KRAS mutation. The prognostic significance of KRAS mutations in patients with non-metastatic colon cancer has not been well elucidated. The National Cancer Database (NCDB) was used to analyze factors associated with KRAS mutation as well as its impact on the presentation and survival of patients with stages I-III colon cancer.
The NCDB was queried to identify patients diagnosed with stages I-III adenocarcinoma of the colon from 2004 to 2015.
A total of 19,877 patients with known KRAS status were identified: mutation rates were 33% in stage I, 35% in stage II, and 38% in stage III patients (p < 0.01). On multivariable analysis, black race and right-sided location were independently associated with KRAS-mutated cancers (all p < 0.01). On univariate analysis for overall survival (OS), KRAS mutation was not significantly associated with a worse 5-year OS for stages I and II patients (p = 0.60 and 0.88, respectively). However, stage III KRAS-mutated colon cancers had a lower OS as compared with KRAS wild type cancers both on univariate and multivariable analysis. Right-sided colon cancers were independently associated with a worse prognosis compared with left-sided lesions (p < 0.01).
KRAS-mutated colon cancers were more frequently observed in black patients, right-sided locations, and higher-stage tumors. These mutations had a negative prognostic impact for stage III patients, suggesting that the incorporation of genotypic data into colon cancer staging may help to guide systemic therapy and prognostication of colon cancer patients.
大约 40%的结直肠癌存在 KRAS 突变。KRAS 突变在非转移性结肠癌患者中的预后意义尚未得到充分阐明。本研究使用国家癌症数据库(NCDB)分析与 KRAS 突变相关的因素,以及其对 I-III 期结肠癌患者表现和生存的影响。
NCDB 用于鉴定 2004 年至 2015 年间诊断为 I-III 期结肠癌腺癌的患者。
共确定了 19877 例 KRAS 状态已知的患者:I 期、II 期和 III 期患者的突变率分别为 33%、35%和 38%(p<0.01)。多变量分析显示,黑种人和右侧位置与 KRAS 突变型癌症独立相关(均 p<0.01)。在总生存(OS)的单变量分析中,KRAS 突变与 I 期和 II 期患者的 5 年 OS 无显著相关性(分别为 p=0.60 和 0.88)。然而,与 KRAS 野生型相比,III 期 KRAS 突变型结肠癌的 OS 在单变量和多变量分析中均较低。右侧结肠癌与左侧病变相比,预后较差(p<0.01)。
KRAS 突变型结肠癌在黑种人、右侧位置和更高分期的肿瘤中更为常见。这些突变对 III 期患者的预后有负面影响,这表明将基因型数据纳入结肠癌分期可能有助于指导结肠癌患者的系统治疗和预后判断。