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TERT 启动子突变的成人 IDH 野生型星形细胞瘤的放射学特征和自然史。

Radiological Characteristics and Natural History of Adult IDH-Wildtype Astrocytomas with TERT Promoter Mutations.

机构信息

Hospices Civils de Lyon, Groupe Hos-pitalier Est, Service de Neuro-Oncologie, Lyon, France.

Unit of Neuro-Oncology, Hospital Universitari de Bellvitge-ICO L'Hospitalet-IDIBELL, l'Hospitalet de Llo-bregat, Barcelona, Spain.

出版信息

Neurosurgery. 2019 Sep 1;85(3):E448-E456. doi: 10.1093/neuros/nyy513.

Abstract

BACKGROUND

Adult IDH-wildtype astrocytomas with TERT promoter mutations (TERTp) are associated with a poor prognosis.

OBJECTIVE

To analyze the radiological presentation and natural history of adult IDH-wildtype astrocytomas with TERTp.

METHODS

We retrospectively reviewed the characteristics of 40 IDH-wildtype TERTp-mutant astrocytomas (grade II n = 19, grade III n = 21) and compared them to those of 114 IDH-mutant lower grade gliomas (LGG), of 92 IDH-wildtype TERTp-mutant glioblastomas, and of 15 IDH-wildtype TERTp-wildtype astrocytomas.

RESULTS

Most cases of IDH-wildtype TERTp-mutant astrocytomas occurred in patients aged >50 yr (88%) and presented as infiltrative lesions without contrast enhancement (73%) that were localized in the temporal and/or insular lobes (37.5%) or corresponded to a gliomatosis cerebri (43%). Thalamic involvement (33%) and extension to the brainstem (27%) were frequently observed, as was gyriform infiltration (33%). This radiological presentation was different from that of IDH-mutant LGG, IDH-wildtype TERTp-mutant glioblastomas, and IDH-wildtype TERTp-wildtype astrocytomas. Tumor evolution before treatment initiation was assessable in 17 cases. Ten cases demonstrated a rapid growth characterized by the apparition of a ring-like contrast enhancement and/or a median velocity of diametric expansion (VDE) ≥8 mm/yr but 7 cases displayed a slow growth (VDE <8 mm/yr) that could last several years before anaplastic transformation. Median overall survival of IDH-wildtype TERTp-mutant astrocytomas was 27 mo.

CONCLUSION

IDH-wildtype TERTp-mutant astrocytomas typically present as nonenhancing temporo-insular infiltrative lesions or as gliomatosis cerebri in patients aged >50 yr. In the absence of treatment, although rapid tumor growth is frequent, an initial falsely reassuring, slow growth can be observed.

摘要

背景

伴 TERT 启动子突变的成人 IDH 野生型星形细胞瘤与不良预后相关。

目的

分析伴 TERT 启动子突变的成人 IDH 野生型星形细胞瘤的影像学表现和自然病程。

方法

我们回顾性分析了 40 例 IDH 野生型 TERTp 突变星形细胞瘤(2 级 n=19,3 级 n=21)的特征,并将其与 114 例 IDH 突变的低级别胶质瘤(LGG)、92 例 IDH 野生型 TERTp 突变的胶质母细胞瘤和 15 例 IDH 野生型 TERTp 野生型星形细胞瘤进行比较。

结果

大多数 IDH 野生型 TERTp 突变星形细胞瘤发生于年龄>50 岁的患者(88%),表现为无强化的浸润性病变(73%),位于颞叶和/或岛叶(37.5%)或符合大脑胶质瘤病(43%)。丘脑受累(33%)和脑干延伸(27%)很常见,也有脑回样浸润(33%)。这种影像学表现与 IDH 突变的 LGG、IDH 野生型 TERTp 突变的胶质母细胞瘤和 IDH 野生型 TERTp 野生型星形细胞瘤不同。在开始治疗前可评估 17 例肿瘤的演变。10 例表现为快速生长,特征为出现环状强化和/或直径膨胀的平均速度(VDE)≥8mm/yr,但 7 例表现为缓慢生长(VDE<8mm/yr),在发生间变之前可能持续数年。IDH 野生型 TERTp 突变星形细胞瘤的中位总生存期为 27 个月。

结论

IDH 野生型 TERTp 突变星形细胞瘤在年龄>50 岁的患者中通常表现为无强化的颞叶-岛叶浸润性病变或大脑胶质瘤病。在未治疗的情况下,尽管快速肿瘤生长很常见,但也可以观察到最初看似令人安心的缓慢生长。

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