Division of Colon and Rectal Surgery, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-Cho, Sunto-Gun, Shizuoka, 411-8777, Japan.
Department of Gastrointestinal Surgery, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-Ku, Tokyo, 113-8510, Japan.
Int J Clin Oncol. 2024 Dec;29(12):1887-1895. doi: 10.1007/s10147-024-02626-9. Epub 2024 Sep 17.
The association between the molecular profiles and prognosis of Stage II colorectal cancer remains unclear. This study aimed to examine the risk factors for relapse of Stage II colorectal cancer using molecular profiling.
We retrospectively enrolled patients with pStage II colorectal cancer who did not receive perioperative adjuvant therapy and whose surgically resected specimens were evaluated using gene expression and whole-exome analyses between January 2014 and December 2018. We evaluated the long-term outcomes and examined the risk factors for relapse-free survival.
We evaluated 322 patients with pStage II colorectal cancer, including 126 (39.1%) with right colon cancer. Eighty-seven patients (27.0%) had pT4 tumor, 175 (54.3%) had positive venous invasion, 120 (37.3%) had positive lymphatic invasion, and 68 (21.1%) had perineural invasion. The presence of mutations in key genes for colorectal cancer development based on whole-exome analyses was as follows: APC, 245 (76.1%); TP53, 208 (64.6%); and KRAS, 134 (41.6%). According to the consensus molecular subtype classification based on gene expression, 76 patients (23.6%) had consensus molecular subtype 4 and a significantly lower relapse-free survival than the other patients (5-year relapse-free survival: 83.8% vs. 92.9%, p = 0.017). Perineural invasion (hazard ratio: 5.316, p < 0.001) and consensus molecular subtype 4 (hazard ratio: 2.399, p = 0.020) were identified as independent risk factors for relapse-free survival.
Molecular profiling of Stage II colorectal cancer to assess the risk factors for relapse may contribute to the indication and drug selection for adjuvant chemotherapy.
分子谱与 II 期结直肠癌预后之间的关联尚不清楚。本研究旨在通过分子谱分析检查 II 期结直肠癌复发的危险因素。
我们回顾性纳入了 2014 年 1 月至 2018 年 12 月期间未接受围手术期辅助治疗且手术切除标本进行基因表达和全外显子分析的 pStage II 结直肠癌患者。我们评估了长期结果,并检查了无复发生存的危险因素。
我们评估了 322 例 pStage II 结直肠癌患者,包括 126 例(39.1%)右结肠癌。87 例(27.0%)患者为 pT4 肿瘤,175 例(54.3%)有静脉侵犯阳性,120 例(37.3%)有淋巴血管侵犯阳性,68 例(21.1%)有神经周围侵犯。基于全外显子分析的结直肠癌发生关键基因的突变情况如下:APC,245 例(76.1%);TP53,208 例(64.6%);KRAS,134 例(41.6%)。根据基因表达的共识分子亚型分类,76 例(23.6%)患者为共识分子亚型 4,无复发生存率明显低于其他患者(5 年无复发生存率:83.8% vs. 92.9%,p=0.017)。神经周围侵犯(危险比:5.316,p<0.001)和共识分子亚型 4(危险比:2.399,p=0.020)被确定为无复发生存的独立危险因素。
评估 II 期结直肠癌复发危险因素的分子谱分析可能有助于辅助化疗的适应证和药物选择。