학술논문

Long-Term Update of Stereotactic Radiosurgery for Benign Spinal Tumors
RESEARCH--HUMAN--CLINICAL STUDIES
Document Type
Academic Journal
Source
Neurosurgery. November 2019, Vol. 85 Issue 5, p708, 9 p.
Subject
California
Language
English
ISSN
0148-396X
Abstract
While primary spinal cord tumors are rare and account for a minority (4%8%) of all neoplasms of the central nervous system, meningiomas and nerve sheath tumors, including neurofibromas and schwannomas, [...]
BACKGROUND: Stereotactic radiosurgery (SRS) for benign intracranial tumors is an established standard of care. The widespread implementation of SRS for benign spinal tumors has been limited by lack of long-term data. OBJECTIVE: To update our institutional experience of safety and efficacy outcomes after SRS for benign spinal tumors. METHODS: We performed a retrospective cohort study of 120 patients with 149 benign spinal tumors (39 meningiomas, 26 neurofibromas, and 84 schwannomas) treated with SRS between 1999 and 2016, with follow-up magnetic resonance imaging available for review. The primary endpoint was the cumulative incidence of local failure (LF), with death as a competing risk. Secondary endpoints included tumor shrinkage, symptom response, toxicity, and secondary malignancy. RESULTS: Median follow-up was 49 mo (interquartile range: 25-103 mo, range: 3-216 mo), including 61 courses with >5 yr and 24 courses with >10 yr of follow-up. We observed 9 LF for a cumulative incidence of LF of 2%, 5%, and 12% at 3,5, and 10 yr, respectively. Excluding 10 tumors that were previously irradiated or that arose within a previously irradiated field, the 3-, 5-, and 10-yr cumulative incidence rates of LF were 1%, 2%, and 8%, respectively. At last follow-up, 35% of all lesions had decreased in size. With a total of 776 patient-years of follow-up, no SRS-related secondary malignancies were observed. CONCLUSION: Comparable to SRS for benign intracranial tumors, SRS provides longer term local control of benign spinal tumors and is a standard-of-care alternative to surgical resection. KEYWORDS: Meningioma, Neurofibroma, Radiosurgery, Schwannoma, Spinal tumors DOI: 10.1093/neuros/nyy442