Michael Farris1, Emory R McTyre2, Christina K Cramer2, Ryan Hughes2, David M Randolph2, Diandra N Ayala-Peacock2, J Daniel Bourland2, Jimmy Ruiz3, Kounosuke Watabe4, Adrian W Laxton5, Stephen B Tatter5, Xiaobo Zhou6, Michael D Chan2. 1. Department of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina. Electronic address: mfarris@wakehealth.edu. 2. Department of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina. 3. Department of Medicine (Hematology & Oncology), Wake Forest School of Medicine, Winston-Salem, North Carolina. 4. Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina. 5. Department of Neurosurgery, Wake Forest School of Medicine, Winston-Salem, North Carolina. 6. Center for Bioinformatics & Systems Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Abstract
PURPOSE: Prior statistical models attempted to identify risk factors for time to distant brain failure (DBF) or time to salvage whole-brain radiation therapy (WBRT) to predict the benefit of early WBRT versus stereotactic radiosurgery (SRS) alone. We introduce a novel clinical metric, brain metastasis velocity (BMV), for predicting clinical outcomes after initial DBF following upfront SRS alone. METHODS AND MATERIALS: BMV was defined as the cumulative number of new brain metastases that developed over time since first SRS in years. Patients were classified by BMV into low-, intermediate-, and high-risk groups, consisting of <4, 4 to 13, and >13 new metastases per year, respectively. Histology, number of metastases at the time of first SRS, and systemic disease status were assessed for effect on BMV. RESULTS: Of 737 patients treated at our institution with upfront SRS without WBRT, 286 had ≥1 DBF event. A lower BMV predicted for improved overall survival (OS) following initial DBF (log-rank P<.0001). Median OS for the low, intermediate, and high BMV groups was 12.4 months (95% confidence interval [CI], 10.4-16.9 months), 8.2 months (95% CI, 5.0-9.7 months), and 4.3 months (95% CI, 2.6-6.7 months), respectively. Multivariate analysis showed that BMV remained the dominant predictor of OS, with a hazard ratio of 2.75 for the high BMV group (95% CI, 1.94-3.89; P<.0001) and a hazard ratio of 1.65 for the intermediate BMV group (95% CI, 1.18-2.30; P<.004). A lower BMV was associated with decreased rates of salvage WBRT (P=.02) and neurologic death (P=.008). Factors predictive for a higher BMV included ≥2 initial brain metastases (P=.004) and melanoma histology (P=.008). CONCLUSIONS: BMV is a novel metric associated with OS, neurologic death, and need for salvage WBRT after initial DBF following upfront SRS alone.
PURPOSE: Prior statistical models attempted to identify risk factors for time to distant brain failure (DBF) or time to salvage whole-brain radiation therapy (WBRT) to predict the benefit of early WBRT versus stereotactic radiosurgery (SRS) alone. We introduce a novel clinical metric, brain metastasis velocity (BMV), for predicting clinical outcomes after initial DBF following upfront SRS alone. METHODS AND MATERIALS: BMV was defined as the cumulative number of new brain metastases that developed over time since first SRS in years. Patients were classified by BMV into low-, intermediate-, and high-risk groups, consisting of <4, 4 to 13, and >13 new metastases per year, respectively. Histology, number of metastases at the time of first SRS, and systemic disease status were assessed for effect on BMV. RESULTS: Of 737 patients treated at our institution with upfront SRS without WBRT, 286 had ≥1 DBF event. A lower BMV predicted for improved overall survival (OS) following initial DBF (log-rank P<.0001). Median OS for the low, intermediate, and high BMV groups was 12.4 months (95% confidence interval [CI], 10.4-16.9 months), 8.2 months (95% CI, 5.0-9.7 months), and 4.3 months (95% CI, 2.6-6.7 months), respectively. Multivariate analysis showed that BMV remained the dominant predictor of OS, with a hazard ratio of 2.75 for the high BMV group (95% CI, 1.94-3.89; P<.0001) and a hazard ratio of 1.65 for the intermediate BMV group (95% CI, 1.18-2.30; P<.004). A lower BMV was associated with decreased rates of salvage WBRT (P=.02) and neurologic death (P=.008). Factors predictive for a higher BMV included ≥2 initial brain metastases (P=.004) and melanoma histology (P=.008). CONCLUSIONS:BMV is a novel metric associated with OS, neurologic death, and need for salvage WBRT after initial DBF following upfront SRS alone.
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Authors: Michael C LeCompte; Ryan T Hughes; Michael Farris; Adrianna Masters; Michael H Soike; Claire Lanier; Chase Glenn; Christina K Cramer; Kounosuke Watabe; Jing Su; Jimmy Ruiz; Christopher T Whitlow; Ge Wang; Adrian W Laxton; Stephen B Tatter; Michael D Chan Journal: J Neurooncol Date: 2020-01-01 Impact factor: 4.130
Authors: Claire M Lanier; Ryan Hughes; Tamjeed Ahmed; Michael LeCompte; Adrianna H Masters; William J Petty; Jimmy Ruiz; Pierre Triozzi; Jing Su; Stacy O'Neill; Kuonosuke Watabe; Christina K Cramer; Adrian W Laxton; Stephen B Tatter; Ge Wang; Christopher Whitlow; Michael D Chan Journal: Neurooncol Pract Date: 2019-02-05
Authors: Michael H Soike; Emory R McTyre; Ryan T Hughes; Michael Farris; Christina K Cramer; Michael C LeCompte; Claire M Lanier; Jimmy Ruiz; Jing Su; Kounosuke Watabe; J Daniel Bourland; Michael T Munley; Stacey O'Neill; Adrian W Laxton; Stephen B Tatter; Michael D Chan Journal: J Neurooncol Date: 2018-05-08 Impact factor: 4.130