Leng Jiali, Wu Fei, Zhang Lihui
Division of Obstetrics and Gynecology, The Second Hospital of Jilin University, Jilin University, Changchun, China.
Division of Obstetrics and Gynecology, The Second Hospital of Jilin University, Changchun, China.
Front Oncol. 2022 May 16;12:734948. doi: 10.3389/fonc.2022.734948. eCollection 2022.
Neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), or monocyte-lymphocyte ratio (MLR) has been shown to be related to the poor prognosis of cervical cancer, ovarian cancer, breast cancer, and other malignant tumors, but their role in predicting the prognosis of endometrial cancer is still controversial. Therefore, we conducted this meta-analysis to evaluate the effectiveness of NLR more accurately, PLR, or MLR in predicting the prognosis of endometrial cancer (EC).
This review systematically searched for relevant publications in databases of the Cochrane Library, PubMed, EMBASE, CNKI, WanFang, VIP, and CBM. Pooled hazard ratios (HR) with 95% confidence intervals (95% CI) were determined and used to explore the association between inflammatory biomarkers (NLR, PLR, and MLR) and overall survival (OS), progression-free survival (PFS), and disease-free survival (DFS) in a random-effects model. We also conducted subgroup analysis and publication bias in this meta-analysis. Stata 12.0 was used for statistical analysis.
This meta-analysis contained 14 eligible studies including 5,274 patients. Our results showed that NLR or PLR was associated with OS [NLR: HR, 2.51; 95% CI, 1.70-3.71; 0.001 in univariate analysis (Ua); HR, 1.87; 95% CI, 1.34-2.60; 0.001 in multivariate analysis (Ma); PLR: HR, 2.50; 95% CI, 1.82-3.43; 0.001 in Ua; HR, 1.86; 95% CI, 1.22-2.83; = 0.004 in Ma], but MLR was not associated with OS (HR, 1.44; 95% CI, 0.70-2.95; = 0.325 in Ua; HR, 1.01; 95% CI, 0.39-2.60; =0.987 in Ma). A further subgroup analysis found that the correlations were not affected by race, cutoff value, sample size, or treatment. Our meta-analysis showed that NLR or PLR was associated with DFS (NLR: HR, 2.50; 95% CI, 1.38-4.56; =0.003 in Ua; HR, 2.06; 95% CI, 1.26-3.37, =0.004 in Ma; PLR: HR, 1.91; 95% CI, 1.30-2.81; = 0.001 in Ua), and NLR was associated with PFS only in the univariate analysis (HR, 1.71; 95% CI, 1.04-2.81; =0.035 in Ua; HR, 1.79; 95% CI, 0.65-4.89; =0.257 in Ma), but MLR was not associated with DFS (HR, 0.36; 95% CI, 0.03-4.13; =0.409 in Ua).
Our results indicated that pretreatment NLR and PLR were biomarkers of poor prognosis in patients with endometrial cancer. The results indicated that NLR or PLR was associated with OS and disease-free survival DFS, and NLR was associated with PFS only in univariate analysis, but MLR was not associated with OS or DFS.
中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)或单核细胞与淋巴细胞比值(MLR)已被证明与宫颈癌、卵巢癌、乳腺癌及其他恶性肿瘤的不良预后相关,但其在预测子宫内膜癌预后中的作用仍存在争议。因此,我们进行了这项荟萃分析,以更准确地评估NLR、PLR或MLR在预测子宫内膜癌(EC)预后方面的有效性。
本综述系统检索了Cochrane图书馆、PubMed、EMBASE、中国知网、万方、维普和中国生物医学文献数据库中的相关出版物。采用随机效应模型确定合并风险比(HR)及95%置信区间(95%CI),以探讨炎症生物标志物(NLR、PLR和MLR)与总生存期(OS)、无进展生存期(PFS)和无病生存期(DFS)之间的关联。我们还在这项荟萃分析中进行了亚组分析和发表偏倚分析。使用Stata 12.0进行统计分析。
这项荟萃分析纳入了14项符合条件的研究,共5274例患者。我们的结果显示,NLR或PLR与OS相关[NLR:单因素分析(Ua)中HR为2.51;95%CI为1.70 - 3.71;P = 0.001;多因素分析(Ma)中HR为1.87;95%CI为1.34 - 2.60;P = 0.001;PLR:Ua中HR为2.50;95%CI为1.82 - 3.43;P = 0.001;Ma中HR为1.86;95%CI为1.22 - 2.83;P = 0.004],但MLR与OS无关(Ua中HR为1.44;95%CI为0.70 - 2.95;P = 0.325;Ma中HR为1.01;95%CI为0.39 - 2.60;P = 0.987)。进一步的亚组分析发现,这些相关性不受种族、临界值、样本量或治疗的影响。我们的荟萃分析显示,NLR或PLR与DFS相关(NLR:Ua中HR为2.50;95%CI为1.38 - 4.56;P = 0.003;Ma中HR为2.06;95%CI为1.26 - 3.37,P = 0.004;PLR:Ua中HR为1.91;95%CI为1.30 - 2.81;P = 0.001),且NLR仅在单因素分析中与PFS相关(Ua中HR为1.71;95%CI为1.04 - 2.81;P = 0.035;Ma中HR为1.79;95%CI为0.65 - 4.89;P = 0.257),但MLR与DFS无关(Ua中HR为0.36;95%CI为0.03 - 4.13;P = 0.409)。
我们的结果表明,预处理时的NLR和PLR是子宫内膜癌患者预后不良的生物标志物。结果表明,NLR或PLR与OS和无病生存期DFS相关,NLR仅在单因素分析中与PFS相关,但MLR与OS或DFS均无关。