Current insights and future directions in systemic therapies for gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) in children and adolescents: a critical review of advancements and challenges

Michaela Kuhlen , Katharina Karges , Marina Kunstreich , Maximilian Schmutz , Antje Redlich , Rainer Claus , Constantin Lapa
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Abstract

Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) in children and adolescents are rare and biologically heterogeneous. Due to their low incidence, therapeutic strategies are largely adapted from adult protocols, underscoring a critical need for paediatric-specific evidence.
Surgical resection remains the mainstay of curative treatment for localized disease and should be prioritized before the initiation of systemic therapy whenever feasible. This review synthesizes current knowledge on systemic therapies in paediatric GEP-NENs,
including somatostatin analogues (SSAs), peptide receptor radionuclide therapy (PRRT), chemotherapy, small molecules (e.g., everolimus, sunitinib), and immune checkpoint inhibitors (ICIs). While SSAs remain the mainstay for well-differentiated, somatostatin receptor (SSTR)-positive tumours, emerging data support the safety and potential efficacy of PRRT in paediatric populations, despite limited prospective evidence. Chemotherapy continues to play a role in high-grade or progressive disease, although responses are variable.
Supportive therapies, including high-dose proton pump inhibitors (PPIs), are also important in managing functional tumours and can significantly alleviate clinical symptoms in advanced disease.
Novel approaches, including SSTR antagonists, α- and β-emitting radiopharmaceuticals, and oncolytic virotherapy (e.g., SVV-001), are under active investigation in adults and may inform future paediatric protocols. Resistance mechanisms—particularly to SSAs—highlight the dynamic nature of tumour evolution and the need for individualized strategies.
These insights underscore the importance of molecular profiling and imaging-based SSTR assessment to guide therapeutic selection, particularly in refractory or complex paediatric cases. Future efforts should prioritize international collaboration, the design of rational combination regimens, and the integration of radiomics, genomics, and biomarker-driven approaches to advance precision medicine in paediatric GEP-NENs.
儿童和青少年胃肠胰神经内分泌肿瘤(GEP-NENs)系统治疗的当前见解和未来方向:对进展和挑战的批判性回顾
胃肠胰神经内分泌肿瘤(GEP-NENs)在儿童和青少年是罕见的和生物学异质性。由于其发病率低,治疗策略在很大程度上改编自成人方案,强调了对儿科特异性证据的迫切需要。手术切除仍然是局部疾病根治性治疗的主要方法,在可能的情况下,应优先于全身治疗。这篇综述综合了目前关于儿科GEP-NENs的全身治疗的知识,包括生长抑素类似物(SSAs)、肽受体放射性核素治疗(PRRT)、化疗、小分子(如依维莫司、舒尼替尼)和免疫检查点抑制剂(ICIs)。尽管ssa仍然是治疗分化良好的生长抑素受体(SSTR)阳性肿瘤的主要药物,但新出现的数据支持PRRT在儿科人群中的安全性和潜在疗效,尽管前瞻性证据有限。化疗继续在高度或进展性疾病中发挥作用,尽管反应是可变的。支持性治疗,包括大剂量质子泵抑制剂(PPIs),在治疗功能性肿瘤中也很重要,可以显著缓解晚期疾病的临床症状。新的治疗方法,包括SSTR拮抗剂、释放α和β的放射性药物以及溶瘤病毒疗法(如SVV-001),正在积极研究中,并可能为未来的儿科治疗方案提供信息。耐药机制——尤其是对ssa的耐药机制——强调了肿瘤进化的动态性和个体化策略的必要性。这些见解强调了分子谱分析和基于成像的SSTR评估对指导治疗选择的重要性,特别是在难治性或复杂的儿科病例中。未来的工作应优先考虑国际合作,设计合理的联合方案,并整合放射组学、基因组学和生物标志物驱动的方法,以推进儿科GEP-NENs的精准医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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