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MAPK 抑制治疗小儿低级别胶质瘤的耐药、反弹和复发模式:一种建立国际共识定义的改良 Delphi 方法——国际小儿低级别胶质瘤联盟。

Resistance, rebound, and recurrence regrowth patterns in pediatric low-grade glioma treated by MAPK inhibition: A modified Delphi approach to build international consensus-based definitions-International Pediatric Low-Grade Glioma Coalition.

机构信息

Department of Paediatric Oncology, Royal Belfast Hospital for Sick Children, Northern Ireland, UK.

Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.

出版信息

Neuro Oncol. 2024 Aug 5;26(8):1357-1366. doi: 10.1093/neuonc/noae074.

Abstract

Pediatric low-grade glioma (pLGG) is the most common childhood brain tumor group. The natural history, when curative resection is not possible, is one of a chronic disease with periods of tumor stability and episodes of tumor progression. While there is a high overall survival rate, many patients experience significant and potentially lifelong morbidities. The majority of pLGGs have an underlying activation of the RAS/MAPK pathway due to mutational events, leading to the use of molecularly targeted therapies in clinical trials, with recent regulatory approval for the combination of BRAF and MEK inhibition for BRAFV600E mutated pLGG. Despite encouraging activity, tumor regrowth can occur during therapy due to drug resistance, off treatment as tumor recurrence, or as reported in some patients as a rapid rebound growth within 3 months of discontinuing targeted therapy. Definitions of these patterns of regrowth have not been well described in pLGG. For this reason, the International Pediatric Low-Grade Glioma Coalition, a global group of physicians and scientists, formed the Resistance, Rebound, and Recurrence (R3) working group to study resistance, rebound, and recurrence. A modified Delphi approach was undertaken to produce consensus-based definitions and recommendations for regrowth patterns in pLGG with specific reference to targeted therapies.

摘要

儿童低级别胶质瘤(pLGG)是最常见的儿童脑肿瘤群体。在无法进行治愈性切除的情况下,其自然史是一种慢性疾病,存在肿瘤稳定期和肿瘤进展期。尽管总体生存率较高,但许多患者会经历严重且潜在的终身疾病。大多数 pLGG 由于突变事件而导致 RAS/MAPK 通路的激活,这导致了在临床试验中使用分子靶向治疗,最近监管机构批准了 BRAF 和 MEK 抑制联合用于治疗 BRAFV600E 突变型 pLGG。尽管具有令人鼓舞的活性,但由于耐药性、治疗后肿瘤复发,或在一些患者中报告为在停止靶向治疗后 3 个月内快速反弹生长,治疗期间可能会发生肿瘤生长。在 pLGG 中,这些生长模式的定义尚未得到很好的描述。出于这个原因,国际儿科低级别胶质瘤联盟,一个由医生和科学家组成的全球性组织,成立了耐药性、反弹和复发(R3)工作组,以研究耐药性、反弹和复发。采用改良 Delphi 方法达成共识,为 pLGG 的生长模式制定定义和建议,特别是针对靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be80/11300023/2ad53de5876f/noae074_fig1.jpg

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