Development and Validation of a Novel Prognostic Nomogram for CD5-Positive Diffuse Large B-Cell Lymphoma: A Retrospective Multicenter Study in China

列线图 弥漫性大B细胞淋巴瘤 国际预后指标 医学 内科学 肿瘤科 比例危险模型 CD5型 淋巴瘤 预测模型 回顾性队列研究 生存分析 队列 总体生存率
作者
Ziyuan Shen,Ling Wang,Bingpei Zhang,Tianci Li,Dashan Li,Chenlu He,Yuhao Xue,Ying Wang,Bing‐Zong Li,Qinhua Liu,Hao Zhang,Weiying Gu,Fei Wang,Chunling Wang,Yuye Shi,Jingjing Ye,Taigang Zhu,Yuqing Miao,Shuiping Huang,Wei Sang
出处
期刊:Frontiers in Oncology [Frontiers Media]
卷期号:11 被引量:3
标识
DOI:10.3389/fonc.2021.754180
摘要

CD5-positive diffuse large B-cell lymphoma (CD5+ DLBCL) is a rare subtype of DLBCL with invasive clinical features and poor prognosis. Current clinical variables based on prognostic systems for DLBCL are inadequate to accurately stratify the prognosis of CD5+ DLBCL.A total of 195 CD5+ DLBCL patients were retrospectively recruited from nine centers in Huaihai Lymphoma Working Group. MaxStat analysis was used to identify optimal cutoff points for continuous variables; univariable and multivariable Cox analyses were used for variable selection; Kaplan-Meier curve was used to analyze the value of variables on prognosis; and C-index, Brier score, and decision curve analysis were measured for predicting model performance.The derivation and validation cohorts consisted of 131 and 64 patients. Of the whole cohort, median age at diagnosis was 61 years, of whom 100 (51.28%) were males and the 5-year overall survival rate was 42.1%. MYC, BCL-2, and the coexpression of MYC/BCL-2 could distinguish the survival of CD5+ DLBCL. Multivariable analysis showed that age, IPI, red blood cell count, neutrophil count, MYC expression, and hepatosplenomegaly were independent predictors, and the prognostic nomogram was developed. The C-index of the nomogram was 0.809 in the derivation and 0.770 in the validation cohort. Decision curve analysis proved that compared with IPI, the specific nomogram showed a better identification in CD5+ DLBCL.The proposed nomogram provided a valuable tool for prognosis prediction in patients with CD5+ DLBCL.

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