Aierken Ailikamu, Atabieke Falide, Li Shui-Xue, Li Kai
Department of General Surgery, Children's Hospital of Xinjiang Uygur Autonomous Region, No.393 Aletai Road, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China.
Graduate School of Xinjiang Medical University, Urumqi, Xinjiang Uygur Autonomous Region, China.
Sci Rep. 2025 May 2;15(1):15466. doi: 10.1038/s41598-025-99170-x.
Metastatic neuroblastoma is a highly aggressive pediatric malignancy with poor prognosis. Radiotherapy is commonly used as part of multimodal treatment, but its impact on survival outcomes remains controversial. This study investigates the association between radiotherapy and survival in patients with metastatic neuroblastoma using data from the Surveillance, Epidemiology, and End Results (SEER) database. A retrospective analysis was conducted on 4,850 patients diagnosed with metastatic neuroblastoma from the SEER database (2004-2015). After applying exclusion criteria, 981 patients were included, with 368 receiving radiotherapy. Propensity score matching (PSM) was used to balance baseline characteristics between the radiotherapy and non-radiotherapy groups, resulting in 234 patients in each group. Survival outcomes were analyzed using Kaplan-Meier curves and Cox proportional hazards models. Before PSM, no significant difference in overall survival (OS) and cancer-specific survival (CSS) was observed between patients who received radiotherapy and those who did not. After PSM, there was a trend toward improved OS and CSS in the radiotherapy group, though statistical significance was not reached. Cox regression analysis identified age ≥ 1 year and non-adrenal primary tumor site as significant independent predictors of poorer OS and CSS. Radiotherapy was not an independent predictor of survival in the multivariate analysis, but a trend toward a survival benefit was noted, particularly in patients with larger tumors and those who underwent surgery. Radiotherapy may improve survival in metastatic neuroblastoma patients with large tumors or surgical resection, though its independent benefit remains uncertain. Personalized strategies require integrating updated COG risk stratification with biomarkers and prospective trials assessing long-term outcomes to refine treatment approaches.
转移性神经母细胞瘤是一种侵袭性很强的儿科恶性肿瘤,预后较差。放射治疗通常作为多模式治疗的一部分使用,但其对生存结果的影响仍存在争议。本研究利用监测、流行病学和最终结果(SEER)数据库的数据,调查转移性神经母细胞瘤患者放疗与生存之间的关联。对SEER数据库(2004 - 2015年)中4850例诊断为转移性神经母细胞瘤的患者进行了回顾性分析。应用排除标准后,纳入981例患者,其中368例接受了放射治疗。采用倾向评分匹配(PSM)来平衡放疗组和非放疗组之间的基线特征,每组各有234例患者。使用Kaplan - Meier曲线和Cox比例风险模型分析生存结果。在PSM之前,接受放疗和未接受放疗的患者之间在总生存期(OS)和癌症特异性生存期(CSS)方面未观察到显著差异。PSM之后,放疗组的OS和CSS有改善的趋势,但未达到统计学显著性。Cox回归分析确定年龄≥1岁和非肾上腺原发性肿瘤部位是OS和CSS较差的显著独立预测因素。在多变量分析中,放疗不是生存的独立预测因素,但注意到有生存获益的趋势,特别是在肿瘤较大和接受手术的患者中。放疗可能改善有大肿瘤或接受手术切除的转移性神经母细胞瘤患者的生存,但其独立获益仍不确定。个性化策略需要将更新的儿童肿瘤协作组(COG)风险分层与生物标志物以及评估长期结果的前瞻性试验相结合,以完善治疗方法。