Men Velia, Bahl Praharsh, Jin James Z, Singh Primal Parry, Hill Andrew G
Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
South Auckland Clinical Campus, The University of Auckland, Auckland, New Zealand.
Ann Surg Oncol. 2025 Feb;32(2):1117-1127. doi: 10.1245/s10434-024-16428-w. Epub 2024 Nov 4.
Lymph node status is a well-established prognostic factor for colon cancer, but the optimal number of nodes for accurate staging remains unclear. This study explored the relationship between lymph node yield (LNY) and 5-year mortality rates in colon cancer patients in New Zealand.
Data from the New Zealand Cancer Registry were retrospectively analyzed for patients with TNM stage I, II, and III colon cancer between August 2003 and December 2021, with follow-up until January 2024. The primary outcome was the 5-year all-cause mortality rate, with LNY, age, sex, ethnicity, tumor site, district health board (DHB), and the number of positive nodes as covariates. Statistical analyses included univariate analysis, Cox regression modeling, and chi-squared tests.
LNY was a significant predictor of 5-year mortality risk (hazard ratio 0.985, p < 0.0001), adjusted for age, sex, ethnicity, tumor site, and DHB. The strongest association between LNY and mortality rate was observed at 12 nodes. Further increases in LNY beyond 22 nodes did not lead to statistically significant differences in mortality rates. Lymph node ratio (LNR) was strongly associated with survival in stage III colon cancer, independent of LNY and the number of positive nodes.
Higher LNY is significantly associated with reduced 5-year mortality rates in stage I-III colon cancer up to the 22-node mark. The strong correlation between LNR and mortality highlights its potential value for improving treatment planning in future clinical practice.
淋巴结状态是结肠癌公认的预后因素,但准确分期所需的最佳淋巴结数量仍不明确。本研究探讨了新西兰结肠癌患者的淋巴结获取数量(LNY)与5年死亡率之间的关系。
对新西兰癌症登记处2003年8月至2021年12月期间TNM分期为I、II和III期的结肠癌患者数据进行回顾性分析,随访至2024年1月。主要结局是5年全因死亡率,将LNY、年龄、性别、种族、肿瘤部位、地区卫生委员会(DHB)和阳性淋巴结数量作为协变量。统计分析包括单因素分析、Cox回归建模和卡方检验。
在对年龄、性别、种族、肿瘤部位和DHB进行校正后,LNY是5年死亡风险的显著预测因素(风险比0.985,p < 0.0001)。在12个淋巴结时观察到LNY与死亡率之间的最强关联。LNY超过22个淋巴结后进一步增加并未导致死亡率有统计学显著差异。淋巴结比率(LNR)与III期结肠癌的生存率密切相关,独立于LNY和阳性淋巴结数量。
在达到22个淋巴结之前,较高的LNY与I - III期结肠癌患者5年死亡率降低显著相关。LNR与死亡率之间的强相关性凸显了其在未来临床实践中改善治疗规划的潜在价值。