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间变性神经胶质瘤:分子诊断时代的治疗方法。

Anaplastic Glioma: Treatment Approaches in the Era of Molecular Diagnostics.

机构信息

Division of Neuro-Oncology Mayo Clinic, Rochester, MN, USA.

Division of Medical Oncology Mayo Clinic, Rochester, MN, USA.

出版信息

Curr Treat Options Oncol. 2018 Oct 25;19(12):61. doi: 10.1007/s11864-018-0579-0.

Abstract

The treatment paradigm for anaplastic glioma has shifted, owing to new diagnostic criteria and new phase III clinical trial evidence. In 2016, the WHO classification of brain tumors including diffuse gliomas was redefined to include molecular criteria, often supplanting the morphological appearance of the tumor cells. This was necessary as prognosis is more closely associated with molecular diagnosis than with morphology and grade. Recently, the benefit of adjuvant chemotherapy in addition to radiotherapy has been demonstrated in both anaplastic oligodendroglioma and anaplastic astrocytoma, as well as lower grade gliomas with the most marked benefit evident in IDH-mutated (astrocytoma) and 1p/19q co-deleted (oligodendroglial) tumors. The defining principle of recent breakthroughs has been the benefit of combinatorial therapy (chemo-radiation) as opposed to treatment in series or treatment of either modality after a period of observation upon evidence of progression.

摘要

由于新的诊断标准和 III 期临床试验证据,间变性神经胶质瘤的治疗模式已经发生转变。2016 年,世界卫生组织(WHO)对脑肿瘤(包括弥漫性神经胶质瘤)的分类进行了重新定义,纳入了分子标准,这些标准通常取代了肿瘤细胞的形态外观。这是必要的,因为与形态学和分级相比,预后与分子诊断的关系更为密切。最近,在间变性少突胶质细胞瘤和间变性星形细胞瘤以及 IDH 突变(星形细胞瘤)和 1p/19q 共缺失(少突胶质细胞瘤)肿瘤中,放射治疗加辅助化疗的获益已得到证实,在低级别胶质瘤中获益最为显著。最近的突破原则是联合治疗(化疗-放疗)的获益,而不是序贯治疗或在观察到进展后再进行单一治疗模式的治疗。

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