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Delayed radiation-induced myelopathy after spinal radiosurgery
Iris C Gibbs1, Chirag Patil, Peter C Gerszten
1Department of Radiation Oncology, Stanford University Medical Center, Stanford, California 94305-5847, USA. iris.gibbs@stanford.edu
Neurosurgery
|January 24, 2009
Summary
Delayed myelopathy after spinal radiosurgery is uncommon. Half of patients experiencing this complication received spinal cord doses exceeding 8 Gy, suggesting a need to limit treatment volumes at this level.
Area of Science:
- Neurology
- Radiation Oncology
- Neurosurgery
Background:
- Spinal cord injury is a feared complication of radiotherapy, often limiting treatment aggressiveness for spinal tumors.
- Radiosurgery offers a precise treatment modality, but understanding its potential complications like delayed myelopathy is crucial.
Purpose of the Study:
- To report a case series of patients who developed delayed myelopathy after spinal radiosurgery.
- To analyze clinical and dosimetric factors associated with radiation-induced myelopathy following spinal radiosurgery.
Main Methods:
- Retrospective review of 1075 patients treated with CyberKnife robotic radiosurgery for spinal tumors between 1996 and 2005.
- Prospective clinical and radiographic follow-up assessments.
- Identification of six patients who developed delayed radiation-induced myelopathy.
Main Results:
- Six patients (5 women, 1 man; mean age 48 years) developed delayed myelopathy at a mean of 6.3 months post-treatment.
- Tumors treated included 3 metastatic and 3 benign, with locations in the upper to midthoracic and cervical spine.
- Half of the patients with myelopathy received spinal cord biological equivalent doses exceeding 8 Gy; specific predictive dosimetric factors were not identified.
Conclusions:
- Delayed myelopathy is uncommon with current radiosurgery dose schedules.
- Radiation injury occurred across a spectrum of doses, preventing identification of specific contributing dosimetric factors.
- Recommend limiting spinal cord treatment volume to below an 8-Gy equivalent dose to mitigate myelopathy risk.