Nong Jingying, Wang Ruotian, Zhang Yi
Department of Thoracic Surgery, Xuanwu Hospital, Capital Medical University, Changchun Street 45#, Beijing, 100053, China.
Eur J Med Res. 2025 Apr 21;30(1):312. doi: 10.1186/s40001-025-02527-1.
Lymphocyte-to-C-reactive protein ratio (LCR) has been linked to survival in malignancies. However, most studies are from Asia. The knowledge about the link between LCR levels and risks of all-cause mortality and cause-specific mortality among cancer participants in the US is lacking.
Using multivariable Cox proportional hazards regression, we investigated the associations between LCR and mortalities in 1999 cancer participants from the National Health and Nutrition Examination Survey 1999-2008 with mortality follow-up through December 31, 2019.
The median follow-up time was 156 months. Cancer participants with low LCR levels were associated with increased risks for all-cause and cancer mortality. Based on the full adjustment model, compared to the lowest LCR tertile, the hazard ratios and 95% confidence interval (HR, 95% CI) of all-cause mortality were 0.75 (0.66-0.87) in the second tertile, 0.60 (0.49-0.72) in the top tertile. The HR of cancer mortality was 0.71 (0.52-0.99) in the second tertile and 0.53 (0.35-0.79) in the top tertile. The link between LCR level and all-cause and cancer mortality remained significant when individuals who died within 2 years of follow-up were excluded.
This prospective study provided evidence of inverse associations between LCR levels and all-cause and cause-specific mortalities based on representative noninstitutional US cancer survivors. Integrating LCR assessment in the clinical routine of US cancer patients may aid in identifying cancer individuals at high risk of mortalities.
淋巴细胞与C反应蛋白比值(LCR)与恶性肿瘤患者的生存率相关。然而,大多数研究来自亚洲。在美国癌症患者中,关于LCR水平与全因死亡率和特定病因死亡率之间联系的了解尚少。
我们采用多变量Cox比例风险回归模型,对1999 - 2008年美国国家健康与营养检查调查中的1999名癌症患者进行研究,这些患者的死亡率随访至2019年12月31日,以探究LCR与死亡率之间的关联。
中位随访时间为156个月。LCR水平低的癌症患者全因死亡率和癌症死亡率风险增加。基于完全调整模型,与LCR最低三分位数组相比,第二三分位数组全因死亡率的风险比及95%置信区间(HR,95%CI)为0.75(0.66 - 0.87),最高三分位数组为0.60(0.49 - 0.72)。第二三分位数组癌症死亡率的HR为0.71(0.52 - 0.99),最高三分位数组为0.53(0.35 - 0.79)。排除随访2年内死亡的个体后,LCR水平与全因死亡率和癌症死亡率之间的联系仍然显著。
这项前瞻性研究基于具有代表性的美国非机构化癌症幸存者,提供了LCR水平与全因死亡率和特定病因死亡率之间存在负相关的证据。将LCR评估纳入美国癌症患者的临床常规检查可能有助于识别死亡风险高的癌症患者。