Department of Surgery, Kurume University School of Medicine, 67 Asahi-Machi, Kurume, Fukuoka, 830-0011, Japan.
Department of Surgery, Tokai University, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan.
Int J Clin Oncol. 2024 Sep;29(9):1284-1292. doi: 10.1007/s10147-024-02565-5. Epub 2024 Jun 4.
The efficacy of adjuvant chemotherapy for high-risk stage II colon cancer (CC) has not been well established. Using propensity score matching, we previously reported that the 3-year disease-free survival (DFS) rate was significantly higher in patients treated with uracil and tegafur plus leucovorin (UFT/LV) against surgery alone. We report the final results, including updated 5-year overall survival (OS) rates and risk factor analysis outcomes.
In total, 1902 high-risk stage II CC patients with T4, perforation/penetration, poorly differentiated adenocarcinoma/mucinous carcinoma, and/or < 12 dissected lymph nodes were enrolled in this prospective, non-randomized controlled study based on their self-selected treatment. Oral UFT/LV therapy was administered for six months after surgery.
Of the 1880 eligible patients, 402 in Group A (surgery alone) and 804 in Group B (UFT/LV) were propensity score-matched. The 5-year DFS rate was significantly higher in Group B than in Group A (P = 0.0008). The 5-year OS rates were not significantly different between groups. The inverse probability of treatment weighting revealed significantly higher 5-year DFS (P = 0.0006) and 5-year OS (P = 0.0122) rates in group B than in group A. Multivariate analyses revealed that male sex, age ≥ 70 years, T4, < 12 dissected lymph nodes, and no adjuvant chemotherapy were significant risk factors for DFS and/or OS.
The follow-up data from our prospective non-randomized controlled study revealed a considerable survival advantage in DFS offered by adjuvant chemotherapy with UFT/LV administered for six months over surgery alone in individuals with high-risk stage II CC.
Japan Registry of Clinical Trials: jRCTs031180155 (date of registration: 25/02/2019), UMIN Clinical Trials Registry: UMIN000007783 (date of registration: 18/04/2012).
辅助化疗治疗高危 II 期结肠癌(CC)的疗效尚未得到充分证实。我们先前通过倾向评分匹配法报告称,与单纯手术相比,接受替加氟+尿嘧啶+亚叶酸(UFT/LV)治疗的患者 3 年无疾病生存率(DFS)显著提高。我们报告最终结果,包括更新的 5 年总生存率(OS)和风险因素分析结果。
共有 1902 例高危 II 期 CC 患者(T4、穿孔/穿透、低分化腺癌/黏液腺癌和/或<12 个淋巴结清扫)根据其自行选择的治疗方案,纳入本前瞻性、非随机对照研究。术后给予口服 UFT/LV 治疗 6 个月。
在 1880 例合格患者中,402 例患者(A 组,单纯手术)和 804 例患者(B 组,UFT/LV)进行了倾向评分匹配。B 组的 5 年 DFS 率明显高于 A 组(P=0.0008)。两组间 5 年 OS 率无显著差异。逆概率治疗权重分析显示 B 组 5 年 DFS(P=0.0006)和 5 年 OS(P=0.0122)均显著高于 A 组。多因素分析显示,男性、年龄≥70 岁、T4、<12 个淋巴结清扫和无辅助化疗是 DFS 和/或 OS 的显著危险因素。
我们前瞻性非随机对照研究的随访数据显示,高危 II 期 CC 患者接受 UFT/LV 辅助化疗 6 个月后,DFS 明显优于单纯手术,具有显著生存优势。
日本临床试验注册:jRCTs031180155(注册日期:2019 年 2 月 25 日),UMIN 临床试验注册:UMIN000007783(注册日期:2012 年 4 月 18 日)。