Emory R McTyre1, Michael H Soike2, Michael Farris3, Diandra N Ayala-Peacock4, Jaroslaw T Hepel5, Brandi R Page6, Colette Shen7, Lawrence Kleinberg6, Joseph N Contessa8, Christopher Corso9, Veronica Chiang8, Adrianna Henson-Masters3, Christina K Cramer3, Jimmy Ruiz10, Boris Pasche10, Kounosuke Watabe11, Ralph D'Agostino12, Jing Su12, Adrian W Laxton13, Stephen B Tatter13, John B Fiveash14, Manmeet Ahluwalia15, Rupesh Kotecha16, Samuel T Chao15, Steve E Braunstein17, Albert Attia4, Caroline Chung18, Michael D Chan3. 1. Department of Radiation Oncology, Greenville Health System Cancer Institute, USA. 2. Hazelrig-Salter Radiation Oncology Center, University of Alabama at Birmingham, USA. Electronic address: msoike@uabmc.edu. 3. Department of Radiation Oncology, Wake Forest School of Medicine, USA. 4. Department of Radiation Oncology, Vanderbilt University School of Medicine, USA. 5. Department of Radiation Oncology, Brown University Alpert Medical School, USA. 6. Department of Radiation Oncology, Johns Hopkins School of Medicine, USA. 7. Department of Radiation Oncology, University of North Carolina, USA. 8. Department of Neurosurgery, Yale School of Medicine, USA. 9. Levine Cancer Institute, Carolinas Healthcare System, USA. 10. Department of Medicine, Wake Forest School of Medicine, USA. 11. Department of Cancer Biology, Wake Forest School of Medicine, USA. 12. Department of Biostatistical Sciences, Wake Forest School of Medicine, USA. 13. Department of Neurosurgery, Wake Forest School of Medicine, USA. 14. Hazelrig-Salter Radiation Oncology Center, University of Alabama at Birmingham, USA. 15. Brain Tumor and Neuro-Oncology Center, Neurological Institute, Cleveland Clinic Foundation, USA. 16. Department of Radiation Oncology, Miami Cancer Institute, USA. 17. Department of Radiation Oncology, University of California San Francisco, USA. 18. Department of Radiation Oncology, M.D. Anderson Cancer Center, USA.
Abstract
INTRODUCTION: Brain metastasis velocity (BMV) is a prognostic metric that describes the recurrence rate of new brain metastases after initial treatment with radiosurgery (SRS). We have previously risk stratified patients into high, intermediate, and low-risk BMV groups, which correlates with overall survival (OS). We sought to externally validate BMV in a multi-institutional setting. METHODS: Patients from nine academic centers were treated with upfront SRS; the validation cohort consisted of data from eight institutions not previously used to define BMV. Patients were classified by BMV into low (<4 BMV), intermediate (4-13 BMV), and high-risk groups (>13 BMV). Time-to-event outcomes were estimated using the Kaplan-Meier method. Cox proportional hazards methods were used to estimate the effect of BMV and salvage modality on OS. RESULTS: Of 2829 patients, 2092 patients were included in the validation dataset. Of these, 921 (44.0%) experienced distant brain failure (DBF). Median OS from initial SRS was 11.2 mo. Median OS for BMV < 4, BMV 4-13, and BMV > 13 were 12.5 mo, 7.0 mo, and 4.6 mo (p < 0.0001). After multivariate regression modeling, melanoma histology (β: 10.10, SE: 1.89, p < 0.0001) and number of initial brain metastases (β: 1.52, SE: 0.34, p < 0.0001) remained predictive of BMV (adjusted R2 = 0.06). CONCLUSIONS: This multi-institutional dataset validates BMV as a predictor of OS following initial SRS. BMV is being utilized in upcoming multi-institutional randomized controlled trials as a stratification variable for salvage whole brain radiation versus salvage SRS after DBF.
INTRODUCTION: Brain metastasis velocity (BMV) is a prognostic metric that describes the recurrence rate of new brain metastases after initial treatment with radiosurgery (SRS). We have previously risk stratified patients into high, intermediate, and low-risk BMV groups, which correlates with overall survival (OS). We sought to externally validate BMV in a multi-institutional setting. METHODS:Patients from nine academic centers were treated with upfront SRS; the validation cohort consisted of data from eight institutions not previously used to define BMV. Patients were classified by BMV into low (<4 BMV), intermediate (4-13 BMV), and high-risk groups (>13 BMV). Time-to-event outcomes were estimated using the Kaplan-Meier method. Cox proportional hazards methods were used to estimate the effect of BMV and salvage modality on OS. RESULTS: Of 2829 patients, 2092 patients were included in the validation dataset. Of these, 921 (44.0%) experienced distant brain failure (DBF). Median OS from initial SRS was 11.2 mo. Median OS for BMV < 4, BMV 4-13, and BMV > 13 were 12.5 mo, 7.0 mo, and 4.6 mo (p < 0.0001). After multivariate regression modeling, melanoma histology (β: 10.10, SE: 1.89, p < 0.0001) and number of initial brain metastases (β: 1.52, SE: 0.34, p < 0.0001) remained predictive of BMV (adjusted R2 = 0.06). CONCLUSIONS: This multi-institutional dataset validates BMV as a predictor of OS following initial SRS. BMV is being utilized in upcoming multi-institutional randomized controlled trials as a stratification variable for salvage whole brain radiation versus salvage SRS after DBF.
Authors: Eric J Lehrer; Brianna M Jones; Daniel R Dickstein; Sheryl Green; Isabelle M Germano; Joshua D Palmer; Nadia Laack; Paul D Brown; Vinai Gondi; Jeffrey S Wefel; Jason P Sheehan; Daniel M Trifiletti Journal: Front Oncol Date: 2022-06-30 Impact factor: 5.738
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Authors: Michael T Milano; Veronica L S Chiang; Scott G Soltys; Tony J C Wang; Simon S Lo; Alexandria Brackett; Seema Nagpal; Samuel Chao; Amit K Garg; Siavash Jabbari; Lia M Halasz; Melanie Hayden Gephart; Jonathan P S Knisely; Arjun Sahgal; Eric L Chang Journal: Neuro Oncol Date: 2020-12-18 Impact factor: 12.300
Authors: Gabriel Cassinelli Petersen; Khaled Bousabarah; Tej Verma; Marc von Reppert; Leon Jekel; Ayyuce Gordem; Benjamin Jang; Sara Merkaj; Sandra Abi Fadel; Randy Owens; Antonio Omuro; Veronica Chiang; Ichiro Ikuta; MingDe Lin; Mariam S Aboian Journal: Neurooncol Adv Date: 2022-07-26