Purpose: To evaluate the efficacy of radiotherapy (RT) for WHO grade 1 and 2 intracranial meningiomas, focusing on the impact of post-surgical tumor volume on treatment outcomes.
Methods: Adult patients (≥18 years) with WHO grade 1 or 2 intracranial meningiomas who received RT between January 1, 2019, and April 1, 2022, were identified. Exclusion criteria encompassed known extracranial tumors, preoperative radio- or chemotherapy, and insufficient RT modality data. Patients were treated according to the international guidelines. Tumor recurrence was identified on MRI with a follow-up period until April 2024. Kaplan-Meier estimates for progression-free survival (PFS) calculations and Cox proportional hazard models were performed to evaluate the impact of tumor volume and other covariates on PFS.
Results: Among 113 patients with intracranial meningiomas who received RT, 103 met the inclusion criteria. Of these, 84.5% received photon-based and 15.5% proton-based treatment. The cohort was predominantly female (72.8%) with a mean age of 59 years. The 2-year and 5-year PFS rates were 95.6% and 90% for grade 1 tumors, respectively, and 83.3% for grade 2 tumors. Tumors >21 cm post-surgical pre-RT had a significantly higher risk of progression (HR = 4.35, p = 0.006).
Conclusions: Tumor volume was identified as a key prognostic factor for PFS in WHO grade 1 and 2 intracranial meningiomas treated with RT. A critical post-surgical volume threshold of 21 cm significantly influences 2-year and 5-year PFS rates, with patients exceeding this threshold experiencing a 335% increase in risk of progression.
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http://dx.doi.org/10.1016/j.wneu.2025.123858 | DOI Listing |
BMC Med Genomics
March 2025
Department of Urology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Background: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of overt Cushing's syndrome (CS), which usually manifests as bilateral macronodular adrenal nodules and varying levels of cortisol secretion. Previous studies have shown that ARMC5 play a huge role in the occurrence of PBMAH, which may be inherited to family members and lead to more severe clinical symptoms. ARMC5 variants may be associated with meningiomas, which is also illustrated by our report.
View Article and Find Full Text PDFJ Neurosurg Case Lessons
March 2025
Department of Neurosurgery, Mayo Clinic, Jacksonville, Florida.
Background: Tumor-to-tumor metastasis (TTM) is an exceptionally rare phenomenon. To date, only 12 cases of the metastasis of clear cell renal cell carcinoma (ccRCC) to a meningioma have been reported in the literature. The authors present a unique case of TTM involving ccRCC metastasizing to a meningioma in a patient with a history of both primary cancers.
View Article and Find Full Text PDFJ Pharm Bioallied Sci
December 2024
Department of Neurosurgery, Madurai Medical College, Madurai, Affiliated under The Tamil Nadu Dr. M.G.R. Medical University, Chennai, Tamil Nadu, India.
Parasagittal and falcine meningiomas pose significant challenges to surgical removal due to their close proximity to the superior sagittal sinus and venous structures, posing high complications. The study evaluated the effectiveness of a microsurgical approach in reducing complication rates and achieving good tumor control in parasagittal and falcine meningiomas. A study involving 20 patients with parasagittal and falcine meningiomas underwent surgery at Madurai Medical College between January 2023 and December 2023.
View Article and Find Full Text PDFNeurochirurgie
March 2025
Neurosurgical Oncology Division - Barretos Cancer Hospital, Barretos, SP, Brazil.
Introduction: Meningioma is the most common benign tumor in the central nervous system and may arise from the sphenoid wing region. The tumor can involve the cavernous sinus medially, periorbital and orbital apex structures anteriorly, and infratemporal fossa inferiorly. Surgical approaches more currently used include the fronto-temporal approach, the pterional approach, and even the frontotemporal-orbitozygomatic approach.
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