Preoperative stereotactic radiosurgery for patients with 1-4 brain metastases: A single-arm phase 2 trial outcome analysis (NCT03398694)

dc.contributor.authorAgrawal, Namita
dc.contributor.authorShireman, Jack M.
dc.contributor.authorShiue, Kevin
dc.contributor.authorKamer, Aaron
dc.contributor.authorBoyd, LaKeisha
dc.contributor.authorZang, Yong
dc.contributor.authorMukherjee, Neel
dc.contributor.authorMiller, James
dc.contributor.authorKulwin, Charles
dc.contributor.authorCohen-Gadol, Aaron
dc.contributor.authorPayner, Troy
dc.contributor.authorLin, Chih-Ta
dc.contributor.authorSavage, Jesse J.
dc.contributor.authorLane, Brandon
dc.contributor.authorBohnstedt, Bradley
dc.contributor.authorLautenschlaeger, Tim
dc.contributor.authorSaito, Naoyuki
dc.contributor.authorShah, Mitesh
dc.contributor.authorWatson, Gordon
dc.contributor.authorDey, Mahua
dc.contributor.departmentRadiation Oncology, School of Medicine
dc.date.accessioned2025-06-17T15:41:05Z
dc.date.available2025-06-17T15:41:05Z
dc.date.issued2024-05-08
dc.description.abstractBackground: Stereotactic radiosurgery (SRS) following surgical resection is the standard of care for patients with symptomatic oligo brain metastasis (BM), however, it is associated with 10-15% local failure. Targeting a resection cavity is imprecise, thus preoperative radiosurgery where the target is well-defined may be superior, however, the efficacy of preoperative SRS has not yet been tested in a clinical trial. Methods: We conducted a phase 2, single-arm trial of preoperative SRS followed by surgical resection in patients with 1-4 symptomatic oligo BMs (NCT03398694) with the primary objective of measuring 6-month local control (LC). SRS was delivered to all patients utilizing a gamma knife or linear accelerator as per RTOG-9005 dosing criteria [Shaw E, Scott C, Souhami L, et al. Single dose radiosurgical treatment of recurrent previously irradiated primary brain tumors and brain metastases: final report of RTOG protocol 90-05. Int J Radiat Oncol Biol Phys. 2000;47(2):291-298] based on tumor diameter with the exception that the largest lesion diameter treated was 5 cm with 15 Gy with all SRS treatment given in single fraction dosing. Results: The trial screened 50 patients, 48 patients were treated under the protocol and 32 patients completed the entire follow-up period. Of all the patients who completed the follow-up period, the primary endpoint of 6-month LC was 100% (95% CI: 0.891-1.000; P = .005). Secondary endpoints, presented as medians, were overall survival (17.6 months), progression-free survival (5.3 months), distant in-brain failure (40.8% at 1 year), leptomeningeal failure (4.8% at 1 year), and radiation necrosis (7.7% at 1 year). Conclusions: Our data confirms superior local control in patients who received preoperative SRS when compared to historical controls. Further study with a larger randomized cohort of patients is warranted to fully understand the benefits of preoperative SRS.
dc.eprint.versionFinal published version
dc.identifier.citationAgrawal N, Shireman JM, Shiue K, et al. Preoperative stereotactic radiosurgery for patients with 1-4 brain metastases: A single-arm phase 2 trial outcome analysis (NCT03398694). Neurooncol Pract. 2024;11(5):593-603. Published 2024 May 8. doi:10.1093/nop/npae043
dc.identifier.urihttps://hdl.handle.net/1805/48822
dc.language.isoen_US
dc.publisherOxford University Press
dc.relation.isversionof10.1093/nop/npae043
dc.relation.journalNeuro-Oncology Practice
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectBrain metastases
dc.subjectPhase II clinical trial
dc.subjectStereotactic radiosurgery
dc.titlePreoperative stereotactic radiosurgery for patients with 1-4 brain metastases: A single-arm phase 2 trial outcome analysis (NCT03398694)
dc.typeArticle
ul.alternative.fulltexthttps://pmc.ncbi.nlm.nih.gov/articles/PMC11398945/
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