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儿童神经母细胞瘤:生物学见解、风险分层与多模式治疗进展

英文原题:Neuroblastoma in Childhood: Biological Insights, Risk Stratification, and Advances in Multimodal Therapy.

查看英文原题

Neuroblastoma in Childhood: Biological Insights, Risk Stratification, and Advances in Multimodal Therapy.

PubMed 2026/01/30(内容时间) J Clin Med Q1 · IF 3.3(JCR 2025)

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中文摘要

神经母细胞瘤是儿童期最常见的颅外实体肿瘤,也是儿科患者癌症相关死亡的主要原因之一。该病具有显著的临床和生物学异质性,范围从婴儿期可自发消退的肿瘤到年长儿童中高度侵袭性、治疗耐药的恶性肿瘤。分子生物学和基因组学的进展显著提高了对神经母细胞瘤发病机制的理解,揭示了遗传和表观遗传改变——如MYCN扩增、ALK突变和染色体畸变——在疾病行为和预后中的关键作用。当代风险分层系统现已整合临床、生物学和分子特征,以更精确地指导治疗。管理策略已向风险适应性、多模式方法演变。低危和中危患者通常通过单纯手术或有限化疗即可获得良好结局,而高危神经母细胞瘤则需要强化多模式治疗,包括诱导化疗、手术切除、大剂量化疗联合自体干细胞挽救、放疗和维持治疗。免疫治疗方法的引入,特别是抗GD2单克隆抗体,显著改善了高危疾病的生存率。新兴疗法如靶向药物、放射性药物和细胞免疫治疗正在进一步拓展治疗格局。尽管取得了这些进展,高危和复发神经母细胞瘤仍与显著的发病率和死亡率相关。持续存在的挑战包括治疗耐药、长期毒性和先进疗法可及性的差异。持续进展将取决于将分子谱分析整合到临床决策中、完善风险适配的治疗策略以及扩大国际协作研究。本叙述性综述总结了关于神经母细胞瘤流行病学、生物学、分期和治疗的当前知识,重点介绍了旨在改善患病儿童结局的最新进展和未来方向。

展开英文摘要原文

Neuroblastoma is the most common extracranial solid tumor of childhood and remains a leading cause of cancer-related mortality in pediatric patients. Characterized by marked clinical and biological heterogeneity, the disease ranges from spontaneously regressing tumors in infants to highly aggressive, treatment-resistant malignancies in older children. Advances in molecular biology and genomics have significantly improved understanding of neuroblastoma pathogenesis, revealing the critical role of genetic and epigenetic alterations-such as MYCN amplification, ALK mutations, and chromosomal aberrations-in disease behavior and prognosis. Contemporary risk stratification systems now integrate clinical, biological, and molecular features to guide therapy more precisely. Management strategies have evolved toward risk-adapted, multimodal approaches. Low- and intermediate-risk patients often achieve excellent outcomes with surgery alone or limited chemotherapy, whereas high-risk neuroblastoma requires intensive multimodal treatment including induction chemotherapy, surgical resection, high-dose chemotherapy with autologous stem cell rescue, radiotherapy, and maintenance therapy.

The incorporation of immunotherapeutic approaches, particularly anti-GD2 monoclonal antibodies, has significantly improved survival in high-risk disease. Emerging therapies such as targeted agents, radiopharmaceuticals, and cellular immunotherapies are further expanding the therapeutic landscape. Despite these advances, high-risk and relapsed neuroblastoma remain associated with substantial morbidity and mortality.

Ongoing challenges include treatment resistance, long-term toxicity, and disparities in access to advanced therapies. Continued progress will depend on integrating molecular profiling into clinical decision-making, refining risk-adapted treatment strategies, and expanding international collaborative research efforts. This narrative review summarizes current knowledge on neuroblastoma epidemiology, biology, staging, and treatment, highlighting recent advances and future directions aimed at improving outcomes for affected children.

论文信息

作者
De Bona A、Barbieri M、Rinaldi N、Esposito S
单位
Pediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.Italy
文献类型
综述
期刊
Journal of clinical medicine2026 Jan 30
原文标识
PubMed 41682783 · DOI 10.3390/jcm15031101