Risk Factors for Progression and Toxic Effects After Preoperative Stereotactic Radiosurgery for Patients With Resected Brain Metastases

Author:

Prabhu Roshan S.12,Akinyelu Tobi1,Vaslow Zachary K.3,Matsui Jennifer K.4,Haghighi Neda56,Dan Tu7,Mishra Mark V.8,Murphy Erin S.9,Boyles Susan3,Perlow Haley K.4,Palmer Joshua D.4,Udovicich Cristian5,Patel Toral R.7,Wardak Zabi7,Woodworth Graeme F.8,Ksendzovsky Alexander8,Yang Kailin9,Chao Samuel T.9,Asher Anthony L.110,Burri Stuart H.12

Affiliation:

1. Levine Cancer Institute, Atrium Health, Charlotte, North Carolina

2. Southeast Radiation Oncology Group, Charlotte, North Carolina

3. Cone Health Cancer Center, Greensboro, North Carolina

4. The Ohio State University College of Medicine, Columbus

5. Peter McCallum Cancer Centre, Melbourne, Victoria, Australia

6. Icon Cancer Centre, Epworth Centre, Richmond, Victoria, Australia

7. University of Texas Southwestern Medical Center, Dallas

8. University of Maryland School of Medicine, Baltimore

9. Taussig Cancer Center, Cleveland Clinic, Cleveland, Ohio

10. Carolina Neurosurgery and Spine Associates, Charlotte, North Carolina

Abstract

ImportancePreoperative stereotactic radiosurgery (SRS) has been demonstrated as a feasible alternative to postoperative SRS for resectable brain metastases (BMs) with potential benefits in adverse radiation effects (AREs) and meningeal disease (MD). However, mature large-cohort multicenter data are lacking.ObjectiveTo evaluate preoperative SRS outcomes and prognostic factors from a large international multicenter cohort (Preoperative Radiosurgery for Brain Metastases–PROPS-BM).Design, Setting, and ParticipantsThis multicenter cohort study included patients with BMs from solid cancers, of which at least 1 lesion received preoperative SRS and a planned resection, from 8 institutions. Radiosurgery to synchronous intact BMs was allowed. Exclusion criteria included prior or planned whole-brain radiotherapy and no cranial imaging follow-up. Patients were treated between 2005 and 2021, with most treated between 2017 and 2021.ExposuresPreoperative SRS to a median dose to 15 Gy in 1 fraction or 24 Gy in 3 fractions delivered at a median (IQR) of 2 (1-4) days before resection.Main Outcomes and MeasuresThe primary end points were cavity local recurrence (LR), MD, ARE, overall survival (OS), and multivariable analysis of prognostic factors associated with these outcomes.ResultsThe study cohort included 404 patients (214 women [53%]; median [IQR] age, 60.6 [54.0-69.6] years) with 416 resected index lesions. The 2-year cavity LR rate was 13.7%. Systemic disease status, extent of resection, SRS fractionation, type of surgery (piecemeal vs en bloc), and primary tumor type were associated with cavity LR risk. The 2-year MD rate was 5.8%, with extent of resection, primary tumor type, and posterior fossa location being associated with MD risk. The 2-year any-grade ARE rate was 7.4%, with target margin expansion greater than 1 mm and melanoma primary being associated with ARE risk. Median OS was 17.2 months (95% CI, 14.1-21.3 months), with systemic disease status, extent of resection, and primary tumor type being the strongest prognostic factors associated with OS.Conclusions and RelevanceIn this cohort study, the rates of cavity LR, ARE, and MD after preoperative SRS were found to be notably low. Several tumor and treatment factors were identified that are associated with risk of cavity LR, ARE, MD, and OS after treatment with preoperative SRS. A phase 3 randomized clinical trial of preoperative vs postoperative SRS (NRG BN012) has began enrolling (NCT05438212).

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

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