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靶向儿童肾上腺皮质癌:分子洞察与新兴治疗策略

英文原题:Targeting pediatric adrenocortical carcinoma: Molecular insights and emerging therapeutic strategies.

查看英文原题

Targeting pediatric adrenocortical carcinoma: Molecular insights and emerging therapeutic strategies.

PubMed 2025/04/16(内容时间) Cancer Treat Rev Q1 · IF 10.6(JCR 2025)

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中文摘要

儿童肾上腺皮质癌(pACC)极为罕见且侵袭性强,仅占儿童癌症的0.2%–0.3%。该病具有显著内分泌活性,常与Li-Fraumeni综合征等遗传综合征相关;与成人肾上腺皮质癌(ACC)相比,其临床和分子特征不同。目前治疗主要沿用成人方案,以手术和化疗(包括米托坦)为主。但缺乏儿科特异性数据及大型临床试验,亟需制定个体化治疗策略。分子分型进展发现了可操作靶点,例如Wnt/β-catenin及MAP/ERK通路改变、IGF2过表达和表观遗传失调。免疫检查点抑制剂、CAR-T 细胞疗法及放射性药物等新兴疗法虽有潜力,但在儿童中大多尚未验证。靶向类固醇生成和脂质代谢等代谢脆弱性,为治疗创新提供其他途径。

此外,液体活检和类固醇谱分析等诊断工具有望改善疾病监测和早期检测。尽管对pACC生物学的认识有所进展,将这些发现转化为有效治疗仍面临重大挑战。欧洲儿童罕见肿瘤协作研究组(EXPeRT)等协作,以及儿科特异性临床试验的开发,对于推动该领域至关重要。多学科照护和国际研究合作将成为满足pACC患者未满足需求的关键。通过利用分子生物学发现并加强全球协作,该领域可迈向精准医疗,改善患儿结局和生活质量。扩大临床试验、改进诊断工具并将新疗法纳入治疗方案,对于缩小儿科与成人ACC治疗成效之间的差距至关重要。

展开英文摘要原文

Pediatric adrenocortical carcinoma (pACC) is an exceptionally rare and aggressive malignancy, accounting for only 0. 2-0. 3% of childhood cancers. Characterized by significant endocrine activity and often associated with genetic syndromes such as Li-Fraumeni syndrome, pACC exhibits distinct clinical and molecular profiles compared to adult adrenocortical carcinoma (ACC). Current treatment approaches, largely adapted from adult protocols, center on surgery and chemotherapy, including mitotane.

However, the lack of pediatric-specific data and major clinical trials underscores a pressing need for tailored therapeutic strategies. Advances in molecular profiling have unveiled actionable targets, such as alterations in the Wnt/ -catenin and MAP/ERK pathways, overexpression of IGF2, and epigenetic dysregulation.

Emerging therapies, including immune checkpoint inhibitors, CAR T-cell therapy, and radiopharmaceuticals, hold promise but remain largely untested in pediatric populations. Targeting metabolic vulnerabilities, such as steroidogenesis and lipid metabolism, offers additional avenues for therapeutic innovation.

Furthermore, improved diagnostic tools like liquid biopsy and steroid profiling may enhance disease monitoring and early detection. Despite progress in understanding pACC biology, significant challenges remain in translating these insights into effective treatments. Collaborative efforts, such as the European Cooperative Study Group for Pediatric Rare Tumors (EXPeRT), and the development of pediatric-specific clinical trials are vital for advancing the field.

Multidisciplinary care and international research initiatives will be pivotal in addressing the unmet needs of pACC patients. By leveraging molecular insights and fostering global collaboration, the field can move toward personalized medicine, improving outcomes and quality of life for children with this challenging disease. Expanding clinical trials, refining diagnostic tools, and integrating novel therapies into treatment regimens will be critical in bridging the gap between pediatric and adult ACC treatment success.

论文信息

作者
Kuhlen M、Schmutz M、Kunstreich M、Redlich A、Claus R
单位
Pediatrics and Adolescent Medicine, Faculty of Medicine, University of Augsburg, Stenglinstr. 2, 86156 Augsburg, Germany; Bavarian Cancer Research Center (BZKF), Augsburg, Germany. Electronic address: Michaela.Kuhlen@uk-augsburg.de.Germany
文献类型
综述
期刊
Cancer treatment reviews2025 May
原文标识
PubMed 40258305 · DOI 10.1016/j.ctrv.2025.102942