Construction and Validation of a Novel Nomogram for Predicting the Recurrence of Diffuse Large B Cell Lymphoma Treated with R-CHOP.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacogenomics & Personalized Medicine Pub Date : 2023-01-01 DOI:10.2147/PGPM.S399336
Yuxi Gong, Haitao Yan, Yefan Yang, Boya Zhai, Zhendong Huang, Zhihong Zhang
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引用次数: 1

Abstract

Purpose: To explore recurrence-risk factors of diffuse large B cell lymphoma (DLBCL) and construct a risk nomogram for predicting recurrence.

Patients and methods: A retrospective analysis was performed on 228 DLBCL patients who achieved complete remission after R-CHOP treatment between January 2015 and December 2019. Univariate and multivariate analyses were applied to identify recurrence-related risk factors from the pretreatment evaluation factors covering patients' demographic characteristics, clinical manifestations, serological indicators, pathological and immunohistochemical results. A nomogram was developed based on the above results and validated by the concordance index (C-index), the receiver operating characteristic (ROC) curve, and the calibration curve.

Results: The training and validation cohorts consisted of 160 and 68 patients (randomized by 7:3). Of the whole cohort, 50 of 228 (21.9%) cases recurred during follow-up. Three recurrence-risk factors including BCL2 expression (P = 0.027), CD10 expression (P = 0.021), LDH level (P = 0.004) were identified from multivariate analysis and entered the final nomogram. The C-index of the nomogram was 0.815 in training cohort and 0.797 in the validation cohort, higher than that of IPI system (0.699) and NCCN-IPI system (0.709). And the 1-year, 2-year, 3-year, and 4-year areas under ROC (AUC) were 0.812, 0.850, 0.837, and 0.801, respectively. The calibration curves also showed a good discrimination capability and accuracy.

Conclusion: The novel nomogram incorporating the three independent risk factors (BCL2 expression, CD10 expression and LDH level) provided a valuable tool for predicting DLBCL recurrence.

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预测R-CHOP治疗弥漫性大B细胞淋巴瘤复发的新Nomogram构建与验证
目的:探讨弥漫大B细胞淋巴瘤(DLBCL)复发的危险因素,构建预测复发的危险图。患者和方法:对2015年1月至2019年12月期间接受R-CHOP治疗后完全缓解的228例DLBCL患者进行回顾性分析。采用单因素和多因素分析,从患者的人口学特征、临床表现、血清学指标、病理和免疫组化结果等预处理评价因素中识别与复发相关的危险因素。根据上述结果建立nomogram,并通过一致性指数(C-index)、受试者工作特征(ROC)曲线和校准曲线进行验证。结果:训练组和验证组分别由160例和68例患者组成(按7:3随机分组)。在整个队列中,228例患者中有50例(21.9%)在随访期间复发。多因素分析确定BCL2表达(P = 0.027)、CD10表达(P = 0.021)、LDH水平(P = 0.004) 3个复发危险因素进入最终nomogram。训练组和验证组的nomogram C-index分别为0.815和0.797,高于IPI系统(0.699)和NCCN-IPI系统(0.709)。1年、2年、3年、4年的ROC (AUC)面积分别为0.812、0.850、0.837、0.801。标定曲线具有良好的分辨能力和精度。结论:结合3个独立危险因素(BCL2表达、CD10表达和LDH水平)的新nomogram预测DLBCL复发提供了一种有价值的工具。
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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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