Avinent-Pérez Marta, Westermann Frank, Navarro Samuel, López-Carrasco Amparo, Noguera Rosa
Department of Pathology, Medical School, University of Valencia, 46010 Valencia, Spain; Neuroblastoma Genomics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Neuroblastoma Genomics, German Cancer Research Center (DKFZ), Heidelberg, Germany; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.
Neoplasia. 2025 Feb;60:101106. doi: 10.1016/j.neo.2024.101106. Epub 2024 Dec 28.
The heterogeneous prognosis in neuroblastoma, shaped by telomere maintenance mechanisms (TMMs), notably the alternative lengthening of telomeres (ALT) pathway, necessitates a refined risk classification for high-risk patients. Current systems often lack precision, hindering tailored treatment approaches. This individual participant data (IPD) meta-analysis of survival among ALT-positive patients aims to improve risk classification systems, enhancing therapeutic strategies and patient outcomes.
Following PRISMA-IPD guidelines, we conducted a comprehensive review of neuroblastoma patients retrieved from PubMed, Scopus, and Embase databases until March-2024. Patients were stratified into ALT-positive and TMM-negative subgroups. Overall and event-free survival probabilities were evaluated.
In our cohort of 293 patients (156 ALT-positive, 137 TMM-negative) obtained from eight different studies, ALT-positive individuals displayed lower survival rates than TMM-negative patients. Non-stage 4 ALT-positive patients had reduced overall and event-free survival probabilities compared to their TMM-negative counterparts, indicating potential misclassification. Stage 4 ALT-positive patients similarly showed poorer survival outcomes than non-stage 4 TMM-negative patients, underscoring the significance of ALT in patient prognosis.
Our study highlights poorer outcomes in ALT-positive neuroblastoma patients, emphasizing the need to integrate TMM status into international risk classification guidelines. Standardizing TMM assessment is key for refining treatment strategies, considering the unique biology of ALT-positive patients.
神经母细胞瘤的预后存在异质性,其由端粒维持机制(TMMs)塑造,尤其是端粒替代延长(ALT)途径,这使得对高危患者进行精确的风险分类成为必要。当前的系统往往缺乏精准性,阻碍了个性化治疗方法的实施。这项针对ALT阳性患者生存情况的个体参与者数据(IPD)荟萃分析旨在改进风险分类系统,优化治疗策略并改善患者预后。
遵循PRISMA-IPD指南,我们对截至2024年3月从PubMed、Scopus和Embase数据库检索到的神经母细胞瘤患者进行了全面综述。患者被分为ALT阳性和TMM阴性亚组。评估了总生存率和无事件生存率。
在我们从八项不同研究中获取的293例患者队列(156例ALT阳性,137例TMM阴性)中,ALT阳性个体的生存率低于TMM阴性患者。与TMM阴性患者相比,非4期ALT阳性患者的总生存率和无事件生存率降低,表明可能存在分类错误。4期ALT阳性患者的生存结果同样比非4期TMM阴性患者差,这突出了ALT在患者预后中的重要性。
我们的研究强调了ALT阳性神经母细胞瘤患者预后较差,强调有必要将TMM状态纳入国际风险分类指南。考虑到ALT阳性患者的独特生物学特性,标准化TMM评估是优化治疗策略的关键。