Cipri Selene, Del Baldo Giada, Fabozzi Francesco, Boccuto Luigi, Carai Andrea, Mastronuzzi Angela
Department of Hematology/Oncology, Cell Therapy, Gene Therapies and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Front Oncol. 2023 Jun 15;13:1204829. doi: 10.3389/fonc.2023.1204829. eCollection 2023.
In the past decade significant advancements have been made in the discovery of targetable lesions in pediatric low-grade gliomas (pLGGs). These tumors account for 30-50% of all pediatric brain tumors with generally a favorable prognosis. The latest 2021 WHO classification of pLGGs places a strong emphasis on molecular characterization for significant implications on prognosis, diagnosis, management, and the potential target treatment. With the technological advances and new applications in molecular diagnostics, the molecular characterization of pLGGs has revealed that tumors that appear similar under a microscope can have different genetic and molecular characteristics. Therefore, the new classification system divides pLGGs into several distinct subtypes based on these characteristics, enabling a more accurate strategy for diagnosis and personalized therapy based on the specific genetic and molecular abnormalities present in each tumor. This approach holds great promise for improving outcomes for patients with pLGGs, highlighting the importance of the recent breakthroughs in the discovery of targetable lesions.
在过去十年中,小儿低级别胶质瘤(pLGGs)可靶向病变的发现取得了重大进展。这些肿瘤占所有小儿脑肿瘤的30%-50%,总体预后良好。2021年最新的世界卫生组织(WHO)pLGGs分类强烈强调分子特征对预后、诊断、治疗及潜在靶向治疗具有重要意义。随着分子诊断技术的进步和新应用,pLGGs的分子特征显示,在显微镜下看似相似的肿瘤可能具有不同的遗传和分子特征。因此,新的分类系统基于这些特征将pLGGs分为几个不同的亚型,从而能够根据每个肿瘤中存在的特定遗传和分子异常制定更准确的诊断策略和个性化治疗方案。这种方法有望改善pLGGs患者的治疗结果,凸显了可靶向病变发现方面近期突破的重要性。