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Multi-institutional validation of brain metastasis velocity, a recently defined predictor of outcomes following stereotactic radiosurgery

Authors :
Jaroslaw T. Hepel
Boris Pasche
Ralph B. D'Agostino
Joseph N. Contessa
Stephen B. Tatter
Albert Attia
Brandi R. Page
Christopher D. Corso
Manmeet Ahluwalia
Lawrence Kleinberg
Samuel T. Chao
Caroline Chung
Michael Farris
D.N. Ayala-Peacock
Emory R. McTyre
Colette J. Shen
Christina K. Cramer
Jing Su
Kounosuke Watabe
Jimmy Ruiz
Adrian W. Laxton
Adrianna Henson-Masters
Michael H. Soike
Rupesh Kotecha
Veronica Chiang
John B. Fiveash
Michael D. Chan
Steve Braunstein
Source :
Radiotherapy and Oncology. 142:168-174
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

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.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.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 RThis 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.

Details

ISSN :
01678140
Volume :
142
Database :
OpenAIRE
Journal :
Radiotherapy and Oncology
Accession number :
edsair.doi.dedup.....1f59550ac1bd33e6222d86471e76a007
Full Text :
https://doi.org/10.1016/j.radonc.2019.08.011