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- Sam Q Sun, Albert H Kim, Chunyu Cai, Rory K J Murphy, Todd DeWees, Peter Sylvester, Ralph G Dacey, Robert L Grubb, Keith M Rich, Gregory J Zipfel, Joshua L Dowling, Eric C Leuthardt, Jeffrey R Leonard, John Evans, Joseph R Simpson, Clifford G Robinson, Richard J Perrin, Jiayi Huang, and Michael R Chicoine.
- ‡Washington University School of Medicine, St. Louis, Missouri; and §Department of Neurosurgery, ¶Pathology and Immunology, and ‖Radiation Oncology, Washington University, St. Louis, Missouri.
- Neurosurgery. 2014 Oct 1;75(4):347-54; discussion 354-5; quiz 355.
BackgroundIndications for external beam radiation therapy (EBRT) for atypical meningiomas (AMs) remain unclear.ObjectiveTo analyze features associated with recurrence in AM patients after gross total resection (GTR) and to assess the relative benefit of EBRT in a retrospective cohort study.MethodsOne hundred fifty-one primary AMs after GTR (88 female patients; median follow-up, 45.0 months) were examined for possible predictors of recurrence (age, sex, location, volume, bone involvement, brain invasion). The Fisher exact and Wilcoxon rank-sum tests were used to analyze the association between these predictors and use of EBRT. The impact on recurrence for these predictors and EBRT was analyzed with Kaplan-Meier and Cox regression.ResultsOf 151 patients, 13 (8.6%) experienced recurrence after GTR (median, 47.0 months). Multivariate analysis identified elevated mitotic index (P = .007) and brain invasion (P = .002) as predictors of recurrence. Larger volume (P = .96) was not associated with recurrence but was more likely to prompt EBRT (P = .001). Recurrences occurred in 11 of 112 with GTR (9.8%; median, 44 months) and 2 of 39 with GTR/EBRT (5.1%; median, 133 months). The 2-, 5-, and 10-year progression-free survival rates after GTR vs GTR/EBRT were 97%, 86%, and 68% vs 100%, 100%, and 78%. Kaplan-Meier analysis demonstrated no difference in progression-free survival or overall survival after GTR vs GTR/EBRT (P = .8, P > .99).ConclusionBrain invasion and high mitotic rates may predict recurrence. After GTR of AMs, EBRT appears not to affect progression-free survival and overall survival, suggesting that observation rather than EBRT may be indicated after GTR.
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