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Prognostic value of FOXP3+ regulatory T cells in patients with diffuse large B-cell lymphoma: a systematic review and meta-analysis
被引:5
|作者:
Bai, Yuping
[1
]
He, Tingting
[1
]
Zhang, Liyan
[2
]
Liu, Qianqian
[1
]
Yang, Jing
[1
]
Zhao, Ziru
[1
]
Yang, Kehu
[3
]
Zhang, Min
[4
]
机构:
[1] Gansu Univ Chinese Med, Sch Basic Med, Lanzhou, Peoples R China
[2] Hebei Cangzhou Hosp Integrated Tradit Chinese & W, Dept Pathol, Cangzhou, Peoples R China
[3] Lanzhou Univ, Evidence Based Med Ctr, Sch Basic Med Sci, Lanzhou, Peoples R China
[4] Gansu Prov Hosp, Dept Pathol, Lanzhou, Peoples R China
来源:
BMJ OPEN
|
2022年
/
12卷
/
09期
基金:
中国国家自然科学基金;
关键词:
lymphoma;
immunology;
haematology;
PREDICTS POOR-PROGNOSIS;
TUMOR MICROENVIRONMENT;
EXPRESSION;
RITUXIMAB;
CYCLOPHOSPHAMIDE;
VINCRISTINE;
IMPACT;
D O I:
10.1136/bmjopen-2021-060659
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives We aimed to comprehensively evaluate the relationship between forkhead box P3 (FOXP3(+)) regulatory T cell (Treg) expression and diffuse large B-cell lymphoma (DLBCL) prognosis and to explore the sources of heterogeneity of the results. Design Systematic review and meta-analysis. Data sources We searched the Cochrane Library, PubMed, Embase and Web of Science databases up to 5 December 2021. Eligibility criteria We included studies that analysed the prognostic significance of FOXP3(+) Tregs in DLBCL. We included studies reported in Chinese or English that reported HRs and related 95% CIs for prognosis. Data extraction and synthesis We extracted data from eligible studies. HRs and 95% CIs were used to assess the prognostic value. Results Fourteen eligible studies were identified. FOXP3(+) Treg expression was not associated with overall survival (OS) (HR=0.72, 95% CI 0.45 to 1.16) or progression-free survival (HR=0.86, 95% CI 0.54 to 1.38). The three approaches used to measure FOXP3(+) Treg expression (p(interaction)<0.001) may be the source of the heterogeneity of the results. Subgroup analysis found that a higher expression of FOXP3(+) Tregs was associated with better OS in all populations and in Asians when FOXP3(+) Treg expression was measured by the number of positive cells (HR=0.36 (95% CI 0.22 to 0.58) in the former, HR=0.33 (95% CI 0.20 to 0.55) in the latter) or the percentage of positive cells (HR=0.49 (95% CI 0.27 to 0.89) in the former, HR=0.38 (95% CI 0.21 to 0.70) in the latter). However, when measured by the score, inverse results were found (HR=1.56, 95% CI 1.01 to 2.42). Conclusions Approaches to measuring FOXP3(+) Treg expression might be the major source of heterogeneity in studies of the prognostic significance of FOXP3(+) Tregs in DLBCL. FOXP3(+) Treg expression might be used to predict the prognosis of patients with DLBCL when FOXP3(+) Treg expression is calculated by the number or the percentage of positive cells, especially in Asian populations.
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