| Literature DB >> 32959992 |
Lorena V Baroni1, Carlos Rugilo2, Fabiana Lubieniecki3, Claudia Sampor1, Candela Freytes1, Liana Nobre4, Jordan R Hansford5,6,7, Vajiranee S Malalasekera5, Michal Zapotocky8, Andrew Dodgshun9, Ofelia Cruz Martinez10, Andres Morales La Madrid10, Cinzia Lavarino11, Mariona Suñol12, Stefan Rutkowski13, Ulrich Schuller13,14,15, Eric Bouffet4, Vijay Ramaswamy4,16, Daniel Alderete1.
Abstract
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.Entities:
Keywords: CNS HGNET-MN1; MN1; astroblastoma; ependymoma; neuroepithelial tumor
Year: 2020 PMID: 32959992 DOI: 10.1002/pbc.28627
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167