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C反应蛋白与淋巴细胞比值及血红蛋白与红细胞分布宽度比值作为神经母细胞瘤患儿有效的预后预测指标

C-reactive protein-to-lymphocyte ratio and hemoglobin-to-red cell distribution width ratio as effective prognostic predictors in pediatric patients with neuroblastoma.

作者信息

Wu Qi, Xu Chencheng, Cao Zhiyao, Lv Jingchun, Han Yali, Teng Gebu, Wu Zhou, Tian Feng, Jiang Dapeng

机构信息

Department of Oncology (Ward2), Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200100, People's Republic of China.

Department of Pediatric Surgery, Suzhou Wujiang District Children's Hospital, Suzhou, Jiangsu Province, 215000, People's Republic of China.

出版信息

Eur J Pediatr. 2025 Jul 21;184(8):493. doi: 10.1007/s00431-025-06334-y.

Abstract

UNLABELLED

Inflammatory responses critically influence tumor progression, yet traditional inflammatory biomarkers in neuroblastoma (NB) research lack optimal sensitivity and specificity. This study aimed to evaluate the prognostic value of two pretreatment inflammatory biomarkers: the C-reactive protein-to-lymphocyte ratio (CLR) and hemoglobin-to-red cell distribution width ratio (HRR) in NB patients. A retrospective analysis was conducted on NB patients diagnosed and treated at Shanghai Children's Medical Center (2016-2022). Pretreatment blood parameters (within 1 week before therapy) were utilized to calculate CLR, HRR, and conventional biomarkers. Optimal cutoff values for each inflammatory biomarker were defined separately. Multivariate Cox regression models identified independent prognostic factors, while Kaplan-Meier curves with log-rank tests assessed survival differences. The cohort included 201 NB children (95 males, 106 females; median age, 37 months). CLR and HRR demonstrated clinically significant predictive accuracy (AUC > 0.7) over traditional biomarkers for both progression-free and overall survival. Elevated ferritin (hazard ratio = 0.35; 95% confidence interval, 0.14-0.90; P = 0.030) independently predicted poor short-term outcomes. For long-term survival, high CLR (hazard ratio = 0.20; 95% confidence interval, 0.05-0.86; P = 0.031) and low HRR (hazard ratio = 2.91; 95% confidence interval, 1.19-7.13; P = 0.019) were significant independent predictors. Kaplan-Meier survival curves demonstrated that high CLR and low HRR were associated with poor long-term outcomes in NB patients (P < 0.05). Intergroup comparisons indicated that the high-CLR and low-HRR groups were predominantly composed of high-risk M-stage patients (P < 0.05).

CONCLUSION

CLR and HRR outperform conventional inflammatory biomarkers as pretreatment prognostic indicators in NB. Elevated CLR and reduced HRR were strongly linked with advanced-stage grouping and adverse long-term outcomes and may serve as effective practical tools for enhancing clinical risk stratification in pediatric NB.

WHAT IS KNOWN

•Neuroblastoma is the most common extracranial solid malignancy in children, and inflammatory biomarkers can effectively predict its prognosis.

WHAT IS NEW

•CLR and HRR are cost-effective biomarkers that enhance risk stratification and correlate strongly with adverse long-term prognosis in NB.

摘要

未标注

炎症反应对肿瘤进展具有关键影响,但神经母细胞瘤(NB)研究中的传统炎症生物标志物缺乏最佳的敏感性和特异性。本研究旨在评估两种治疗前炎症生物标志物:C反应蛋白与淋巴细胞比值(CLR)和血红蛋白与红细胞分布宽度比值(HRR)在NB患者中的预后价值。对在上海儿童医学中心诊断和治疗的NB患者(2016 - 2022年)进行了回顾性分析。利用治疗前血液参数(治疗前1周内)计算CLR、HRR和传统生物标志物。分别确定每种炎症生物标志物的最佳临界值。多变量Cox回归模型确定独立的预后因素,而采用对数秩检验的Kaplan - Meier曲线评估生存差异。该队列包括201名NB儿童(95名男性,106名女性;中位年龄37个月)。CLR和HRR在无进展生存期和总生存期方面,相对于传统生物标志物显示出具有临床意义的预测准确性(AUC>0.7)。铁蛋白升高(风险比 = 0.35;95%置信区间,0.14 - 0.90;P = 0.030)独立预测短期预后不良。对于长期生存,高CLR(风险比 = 0.20;95%置信区间,0.05 - 0.86;P = 0.031)和低HRR(风险比 = 2.91;95%置信区间,1.19 - 7.13;P = 0.019)是显著的独立预测因素。Kaplan - Meier生存曲线表明,高CLR和低HRR与NB患者的长期不良预后相关(P<0.05)。组间比较表明,高CLR组和低HRR组主要由高危M期患者组成(P<0.05)。

结论

在NB中,CLR和HRR作为治疗前预后指标优于传统炎症生物标志物。CLR升高和HRR降低与晚期分组及不良长期预后密切相关,可作为增强儿童NB临床风险分层的有效实用工具。

已知信息

•神经母细胞瘤是儿童最常见的颅外实体恶性肿瘤,炎症生物标志物可有效预测其预后。

新发现

•CLR和HRR是具有成本效益的生物标志物,可增强风险分层,且与NB的不良长期预后密切相关。

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