Prognostic and clinicopathological role of geriatric nutritional risk index in patients with diffuse large B-cell lymphoma: A meta-analysis

被引:0
作者
Cao, Dan [1 ]
Zhang, Zongxin [2 ]
机构
[1] Huzhou Univ, Affiliated Cent Hosp, Huzhou Cent Hosp, Dept Hematol, Huzhou, Zhejiang, Peoples R China
[2] Huzhou Univ, Huzhou Cent Hosp, Affiliated Cent Hosp, Clin Lab, Huzhou, Zhejiang, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
关键词
geriatric nutritional risk index; meta-analysis; diffuse large B-cell lymphoma; prognosis; clinical practice; GLOBULIN RATIO; INFLAMMATION; ALBUMIN; CANCER;
D O I
10.3389/fonc.2023.1169749
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Previous studies have explored the relationship between the geriatric nutritional risk index (GNRI) and survival outcomes of diffuse large Bcell lymphoma (DLBCL) cases, but the results were inconsistent. Consequently, the present meta-analysis was conducted to investigate how GNRI affects DLBCL and its function in terms of prognosis. Methods: TheWeb of Science, PubMed, Embase, and Cochrane Library databases were thoroughly searched until January 18, 2023. We calculated combined hazard ratios (HRs) and 95% confidence intervals (CIs) to estimate the relationship between the GNRI and survival outcomes of patients with DLBCL. Results: This meta-analysis included seven articles involving 2,353 cases. A lower level of GNRI predicted dismal overall survival (HR=1.40, 95% CI=1.25-1.56, p< 0.001) and inferior progression-free survival (HR=1.46, 95% CI=1.19-1.80, p<0.001) of DLBCL patients. Moreover, a low GNRI was significantly related to Eastern Cooperative Oncology Group Performance Status =2 (odds ratio [OR] =4.55, 95% CI=2.75-7.54, p<0.001), Ann Arbor stage III-IV (OR=2.91, 95% CI=2.38-3.57, p<0.001), B symptoms (OR=3.51, 95% CI=2.34-5.29, p<0.001), and extranodal disease (OR=2.90, 95% CI=2.32-3.63, p<0.001). Conclusion: A lower GNRI level predicted poorer short- and long- term prognosis in patients with DLBCL. A low GNRI was correlated with clinical factors of disease progression in DLBCL patients.
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