Prognostic significance of the red blood cell distribution width in diffuse large B-cell lymphoma patients
Metrics: PDF 1614 views | HTML 2523 views | ?
Shujuan Zhou1, Fang Fang1, Huiyao Chen1, Wei Zhang1, Yang Chen1, Yifen Shi1, Zhouyi Zheng2, Yongyong Ma1, Liyuan Tang1, Jianhua Feng1, Yu Zhang1, Lan Sun1, Yi Chen1, Bin Liang1, Kang Yu1 and Songfu Jiang1
1Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, P.R. China
2Department of Hematology and oncology, Traditional Chinese Medical Hospital of Zhuji, Shaoxing, Zhejiang, P.R. China
Songfu Jiang, email: firstname.lastname@example.org
Kang Yu, email: email@example.com
Keywords: diffuse large B cell lymphoma, red blood cell distribution width, prognosis, survival
Received: November 30, 2016 Accepted: March 09, 2017 Published: March 25, 2017
This study examined the prognostic value of the baseline red blood cell distribution width (RDW) in diffuse large B cell lymphoma (DLBCL) patients. The associations between RDW and clinical characteristics were assessed in 161 DLBCL patients from 2005 to 2016. The log-rank test, univariate analysis, and Cox regression analysis were used to evaluate the relationship between RDW and survival. A RDW of 14.1% was considered to be the optimal cut-off value for predicting prognosis. A high RDW was associated with more frequent B symptoms (P=0.001), a higher International Prognostic Index score (P=0.032), more extranodal sites of disease (P=0.035), and significantly lower Eastern Cooperative Oncology Group performance status (P=0.031). The log-rank test demonstrated that patients with a high RDW had a shorter overall survival (OS) (2-year OS rate, 53.6% vs. 83.6%, P<0.001) and progression-free survival (PFS) (2-year PFS rate, 44.7% vs. 81.8%, P<0.001). The multivariate analysis demonstrated that RDW ≥14.1% was an independent predictor of OS (odds ratio [OR] = 0.345, P<0.001) and PFS (OR = 0.393, P=0.001). We demonstrated that a high RDW predicted an unfavorable prognosis in patients with DLBCL.
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.