Team studies association between tumor mutations and meningioma recurrence in Grade I/II disease

A new research paper titled "Association between tumor mutations and meningioma recurrence in Grade I/II disease" has been published inOncoscience.

Meningiomas are common intracranial tumors with variable prognoses not entirely captured by commonly used classification schemes. In this new study, researchers from Icahn School of Medicine at Mount Sinai and Sema4 (A Mount Sinai Venture) sought to determine the relationship between meningioma mutations and oncologic outcomes using a targeted next-generation sequencing panel.

The researchers note, "As such, there is a need to further characterize meningioma disease mechanisms in pursuit of better diagnostics and novel targets to improve treatment paradigms."

The team identified 184 grade I and II meningiomas with both more than 90 days of post-surgical follow-up and linked targeted next-generation sequencing. For mutated genes in greater than 5% of the sample, progression-free survival Cox-regression models stratified by gene were computed. The researchers then built a multi-gene model by including all gene predictors with a p-value of less than 0.20. Starting with that model, the researchers performed backward selection to identify the most predictive factors.

ATM (HR = 4.448; 95% CI: 1.517-13.046), CREBBP (HR = 2.727; 95% CI = 1.163-6.396), and POLE (HR = 0.544; HR = 0.311-0.952) were significantly associated with alterations in disease progression after adjusting for clinical and pathologic factors. In the multi-gene model, only POLE remained a significant predictor ofrecurrence协变量调整后的临床。Backwards selection identified recurrence status, resection extent, and mutations in ATM (HR = 7.333; 95% CI = 2.318-23.195) and POLE (HR = 0.413; 95% CI = 0.229-0.743) as predictive of recurrence.

"Mutations in ATM and CREBBP were associated with acceleratedmeningiomarecurrence, and mutations in POLE were protective of recurrence. Each mutation has potential implications for treatment. The effect of these mutations on oncologic outcomes and as potential targets for intervention warrants future study," the researchers conclude.