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Association of frequent NF2 mutations with spinal location predominance and worse outcomes in psammomatous meningiomas.
Ren, Leihao; Xie, Qing; Deng, Jiaojiao; Chen, Jiawei; Yu, Jinxiu; Wang, Daijun; Wakimoto, Hiroaki; Gong, Ye; Hua, Lingyang.
Afiliación
  • Ren L; 1Departments of Neurosurgery and.
  • Xie Q; 2Institute of Neurosurgery, Fudan University, Shanghai, China.
  • Deng J; 3Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Fudan University, Shanghai, China; and.
  • Chen J; 1Departments of Neurosurgery and.
  • Yu J; 2Institute of Neurosurgery, Fudan University, Shanghai, China.
  • Wang D; 3Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Fudan University, Shanghai, China; and.
  • Wakimoto H; 1Departments of Neurosurgery and.
  • Gong Y; 2Institute of Neurosurgery, Fudan University, Shanghai, China.
  • Hua L; 3Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Fudan University, Shanghai, China; and.
J Neurosurg ; 141(3): 593-601, 2024 Sep 01.
Article en En | MEDLINE | ID: mdl-38552238
ABSTRACT

OBJECTIVE:

Psammomatous meningiomas (PMs) are a rare histological subtype of meningioma but are rather frequent in spinal meningiomas. The authors aimed to analyze the incidence, clinical features, molecular alterations, long-term outcomes, and prognostic factors of PMs.

METHODS:

In total, 151 patients with PMs were included in this study. Clinical characteristics, molecular alterations, and progression-free survival (PFS) were analyzed in PMs. Clinical characteristics were compared between PMs and other WHO grade 1 meningiomas. Targeted sequencing of meningioma-relevant genes was performed to determine the molecular alterations in PMs.

RESULTS:

PMs accounted for 1.34% of all meningiomas. Clinically, spinal location (p < 0.001) and female predominance (p < 0.001) were statistically significant in PMs when compared with the other grade 1 subtypes. Radiologically, calcification was frequently found in PMs (88.24%). Genetically, NF2 was the most frequently mutated gene in PMs (59.7%), followed by TRAF7 and AKT1. Ten patients experienced recurrence during the long-term follow-up. Multivariate analysis demonstrated that age (p = 0.009), extent of resection (p < 0.001), Ki-67 index (p = 0.007), and NF2 status (p < 0.001) were independent prognostic factors in the cohort of PMs. Interestingly, NF2 mutation was detected in all (48/48) spinal PMs (SPMs) but in only 38.46% (35/91) of cranial PMs (CPMs), revealing a significant difference (p < 0.001). The mean Ki-67 index (p = 0.044) and proportion of PMs with PR-positive expression (p = 0.048) were significantly higher in SPMs than in CPMs. The frequent NF2 mutations are associated with spinal location predominance and worse PFS in PMs.

CONCLUSIONS:

Female sex and spinal location predominance were statistically significant in PMs. NF2 mutation was an independent predictor for worse PFS of PMs. Of note, NF2 mutation was detected in all SPMs but in only 38.46% of CPMs, revealing a significant difference.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromina 2 / Neoplasias Meníngeas / Meningioma / Mutación Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurosurg Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromina 2 / Neoplasias Meníngeas / Meningioma / Mutación Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurosurg Año: 2024 Tipo del documento: Article
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