Prognostic role of lymphocyte to monocyte ratio for patients with cancer: evidence from a systematic review and meta-analysis

被引:135
作者
Gu, Liangyou [1 ]
Li, Hongzhao [1 ]
Chen, Luyao [1 ]
Ma, Xin [1 ]
Li, Xintao [1 ]
Gao, Yu [1 ]
Zhang, Yu [1 ]
Xie, Yongpeng [1 ,2 ]
Zhang, Xu [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, PLA Med Sch, Dept Urol, State Key Lab Kidney Dis, Beijing 100853, Peoples R China
[2] Nankai Univ, Sch Med, Tianjin 300071, Peoples R China
关键词
inflammation; lymphocyte to monocyte ratio; cancer; prognosis; meta-analysis; B-CELL LYMPHOMA; PREDICTS UNFAVORABLE PROGNOSIS; TUMOR-ASSOCIATED MACROPHAGES; LOW PREOPERATIVE LYMPHOCYTE; INFLAMMATORY RESPONSE; SOLID TUMORS; SURVIVAL; DIAGNOSIS; COUNT; PROGRESSION;
D O I
10.18632/oncotarget.7876
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inflammation influences cancer development and progression, and a low lymphocyte to monocyte ratio (LMR) has been reported to be a poor prognostic indicator in several malignancies. Here we quantify the prognostic impact of this biomarker and assess its consistency in various cancers. Eligible studies were retrieved from PubMed, Embase and Web of Science databases. Overall survival (OS) was the primary outcome, cancer-specific survival (CSS), disease-free survival (DFS), recurrence-free survival (RFS), and progression-free survival (PFS) were secondary outcomes. Pooled hazard ratios (HRs), odds ratios (ORs), and 95% confidence intervals (CIs) were calculated. Fifty-six studies comprising 20,248 patients were included in the analysis. Overall, decreased LMR was significantly associated with shorter OS in non-hematological malignancy (HR: 0.59, 95% CI: 0.53-0.66; P < 0.001) and hematological malignancy (HR: 0.44, 95% CI: 0.34-0.56; P < 0.001). Similar results were found in CSS, DFS, RFS and PFS. Moreover, low LMR was significantly associated with some clinicopathological characteristics that are indicative of poor prognosis and disease aggressiveness. By these results, we conclude that a decreased LMR implied poor prognosis in patients with cancer and could serve as a readily available and inexpensive biomarker for clinical decision.
引用
收藏
页码:31926 / 31942
页数:17
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