Mantalovas Stylianos, Karakousis Vasileios Alexandros, Sevva Christina, Roulia Panagiota, Savvakis Stavros, Anthimidis Georgios, Papadopoulos Konstantinos, Magra Vasiliki, Varsamis Nikolaos, Kosmidis Christoforos S, Kesisoglou Isaak
3rd Surgical Department, AHEPA University Hospital of Thessaloniki, School of Medicine, Aristotle University of Thessaloniki, 1st St. Kiriakidi Street, 54621 Thessaloniki, Greece.
Plastic Surgery Department, Papageorgiou General Hospital of Thessaloniki, School of Medicine, Aristotle University of Thessaloniki, Ring Road, 56403 Thessaloniki, Greece.
Cancers (Basel). 2025 Jun 10;17(12):1934. doi: 10.3390/cancers17121934.
: The present investigation quantifies the striking predisposition for small intestinal GISTs in NF-1 patients, examining both multifocal and solitary tumor patterns while establishing critical epidemiological comparisons with the general population. By elucidating these distinct clinical and biological profiles, the study aims to transform the understanding of NF1-associated tumorigenesis and optimize patient surveillance strategies. : This systematic review and meta-analysis was conducted in strict accordance with PRISMA guidelines, the gold-standard framework for minimizing bias and maximizing reproducibility in evidence synthesis. Prospectively registered in PROSPERO, the study employed a PICO framework to evaluate interventions, outcomes, and comparisons. : This systematic review and meta-analysis reveals a profound oncogenic propensity for small intestinal GISTs in NF-1 patients, demonstrating markedly increased prevalence relative to population baselines. The tumors display characteristic presentation and histological profiles, with a distribution of 54% multifocal lesions, 41% solitary SI-GIST, and 5% solitary duodenal GIST cases, demonstrating the diverse clinical manifestations of NF-1-associated tumors. These compelling findings not only redefine the epidemiological landscape of NF1-associated malignancies but also underscore extraordinary disease susceptibility, far surpassing previous estimates and sporadic occurrence rates in the general population. : The distinct clinical patterns and high frequency of these tumors among NF-1 patients provide important insights into GIST development while underscoring the need for heightened clinical suspicion, particularly in patients manifesting gastrointestinal hemorrhage. These findings highlight the unique challenges in managing these cases-including diagnostic limitations and therapeutic constraints-underscoring the imperative for multidisciplinary therapeutic frameworks for detection, monitoring and treatment in this high-risk population.
本研究对神经纤维瘤病1型(NF-1)患者小肠胃肠道间质瘤(GIST)的显著易感性进行了量化,研究了多灶性和孤立性肿瘤模式,并与普通人群进行了关键的流行病学比较。通过阐明这些不同的临床和生物学特征,该研究旨在改变对NF1相关肿瘤发生的理解,并优化患者监测策略。
本系统评价和荟萃分析严格按照PRISMA指南进行,PRISMA指南是在证据综合中最小化偏倚和最大化可重复性的金标准框架。该研究在PROSPERO中进行了前瞻性注册,采用PICO框架来评估干预措施、结局和比较。
本系统评价和荟萃分析揭示了NF-1患者小肠GIST有显著的致癌倾向,相对于人群基线,其患病率显著增加。这些肿瘤表现出特征性的临床表现和组织学特征,其中54%为多灶性病变,41%为孤立性小肠GIST,5%为孤立性十二指肠GIST病例,显示了NF-1相关肿瘤的多样临床表现。这些令人信服的发现不仅重新定义了NF1相关恶性肿瘤的流行病学格局,也凸显了其极高的疾病易感性,远远超过先前的估计以及普通人群中的散发病例发生率。
这些肿瘤在NF-1患者中的独特临床模式和高频率为GIST的发展提供了重要见解,同时强调了提高临床怀疑度的必要性,特别是在出现胃肠道出血的患者中。这些发现突出了管理这些病例的独特挑战,包括诊断局限性和治疗限制,强调了在这个高风险人群中建立多学科治疗框架以进行检测、监测和治疗的紧迫性。