Service of Hematology/Oncology, Hospital JP Garrahan, Buenos Aires, Argentina.
Service of Diagnostic Imaging, Hospital JP Garrahan, Buenos Aires, Argentina.
Pediatr Blood Cancer. 2020 Dec;67(12):e28627. doi: 10.1002/pbc.28627. Epub 2020 Sep 22.
Central nervous system high-grade neuroepithelial tumor with MN1 alteration (CNS HGNET-MN1) is a rare recently described entity. Fourteen CNS HGNET-MN1 patients were identified using genome-wide methylation arrays/RT-PCR across seven institutions. All patients had surgery (gross total resection: 10; subtotal resection: four) as initial management followed by observation alone in three patients, followed by radiotherapy in eight patients (focal: five; craniospinal: two; CyberKnife: one) and systemic chemotherapy in three patients. Seven patients relapsed; five local and two metastatic, despite adjuvant radiotherapy, of which three died. Treatment of CNS HGNET-MN1 remains a major treatment challenge despite aggressive surgical resections and upfront radiotherapy, warranting new approaches to this rare malignancy.
中枢神经系统高级别神经上皮肿瘤伴 MN1 改变(CNS HGNET-MN1)是一种罕见的新描述实体。通过七个机构的全基因组甲基化阵列/RT-PCR 共鉴定出 14 名 CNS HGNET-MN1 患者。所有患者均接受手术治疗(完全切除:10 例;次全切除:4 例)作为初始治疗,随后仅在 3 名患者中进行观察,在 8 名患者中进行放疗(局部:5 例;颅脊髓:2 例;CyberKnife:1 例),在 3 名患者中进行全身化疗。7 名患者复发;5 例局部复发,2 例远处转移,尽管进行了辅助放疗,但其中 3 名患者死亡。尽管进行了积极的手术切除和放疗,但中枢神经系统高级别神经上皮肿瘤伴 MN1 改变的治疗仍然是一个重大挑战,需要针对这种罕见的恶性肿瘤采取新的治疗方法。