Related Experiment Video
Updated: Jan 24, 2026

02:22
Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
Published on: April 12, 2024
917
Radiosurgery for Chordoma and Chondrosarcoma.
Hideyuki Kano1, Ajay Niranjan2, L Dade Lunsford2
1Department of Neurological Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA, kanoh@upmc.edu.
Progress in Neurological Surgery
|May 17, 2019
Summary
Chordomas and chondrosarcomas are rare skull base tumors. Stereotactic radiosurgery (SRS) is evaluated as a key treatment for recurrent or residual tumors after surgery and radiation.
Area of Science:
- Oncology
- Neurosurgery
- Radiation Oncology
Background:
- Chordomas and chondrosarcomas are rare, locally aggressive skull base tumors.
- These tumors have high rates of progression and recurrence.
- Effective management often requires multimodality treatment, including surgery, radiation therapy, and stereotactic radiosurgery (SRS).
Purpose of the Study:
- To examine the role and efficacy of stereotactic radiosurgery (SRS) in managing skull base chordomas and chondrosarcomas.
- To review SRS as a treatment option for patients with recurrent or residual tumors.
Main Methods:
- Review of existing literature and clinical data on SRS for skull base chordomas and chondrosarcomas.
- Analysis of treatment outcomes, including progression-free survival and local control rates.
- Evaluation of SRS in the context of multimodality treatment protocols.
Main Results:
- Stereotactic radiosurgery (SRS) is a recognized management option for skull base chordomas and chondrosarcomas.
- SRS is particularly utilized for recurrent or residual tumors following initial surgical resection and fractionated radiation therapy.
- The effectiveness of SRS in controlling tumor progression and recurrence is a key focus.
Conclusions:
- Stereotactic radiosurgery (SRS) plays a significant role in the multimodality management of skull base chordomas and chondrosarcomas.
- SRS offers a valuable therapeutic option for patients with challenging recurrent or residual disease.
- Further investigation into optimal SRS protocols may enhance outcomes for these rare tumors.

