Fernández María Baro, Alonso Vanesa Pérez
Department of Pediatric Hemato-Oncology, Hospital 12 de Octubre, Madrid, Spain.
Childs Nerv Syst. 2016 Oct;32(10):1939-45. doi: 10.1007/s00381-016-3132-0. Epub 2016 Sep 20.
Pediatric low-grade gliomas (PLGG) are the most common primary central nervous system tumor in children. Patients in whom gross total resection can be achieved have an excellent overall (OS) and event-free survival (EFS) and do not require adjuvant therapy. However, children with unresectable tumors often experience multiple progressions and require additional treatment.
Radiotherapy results in long-term tumor control, but it is associated with significant toxicity, making chemotherapy the preferred therapeutic option. Several chemotherapy combinations have been found to be successful in PLGG, but 5-year EFS has been below 60 % with most of them.
MOLECULAR-BASED TREATMENT: Recent molecular advances have led to a better understanding of the molecular pathways involved in the biology of LGG, allowing the development of promising tumor-specific, molecularly targeted therapies.
小儿低级别胶质瘤(PLGG)是儿童最常见的原发性中枢神经系统肿瘤。能够实现肿瘤全切的患者具有出色的总生存期(OS)和无事件生存期(EFS),且无需辅助治疗。然而,患有无法切除肿瘤的儿童常经历多次病情进展,需要额外治疗。
放疗可实现长期肿瘤控制,但会带来显著毒性,因此化疗成为首选治疗方案。已发现几种化疗联合方案在小儿低级别胶质瘤治疗中取得成功,但其中大多数方案的5年无事件生存率低于60%。
最近的分子研究进展使人们对低级别胶质瘤生物学中涉及的分子途径有了更深入的了解,从而得以开发出有前景的肿瘤特异性分子靶向疗法。