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Standard Dose Versus High Dose Stereotactic Spine Radiosurgery for Metastatic Spinal Neoplasms - SHINE: A Prospective Randomized Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this clinical trial is to learn if a higher dose of Stereotactic Spine Radiosurgery (SSRS), an advanced radiation technique, is better for treating cancer that has spread to the spine (spinal metastases). The study will also learn about the safety of using a higher dose. The main questions it aims to answer are: Does a higher radiation dose lead to fewer treatment failures (meaning the tumor growing back or causing serious side effects) one year after treatment? What are the side effects associated with the high dose compared to the standard dose? How does each radiation dose affect a patient's pain and quality of life? Researchers will randomly assign participants (like a coin toss) to one of two groups to compare the outcomes: The Standard Dose Group: Will receive a single radiation treatment of 16 Gy. The High Dose Group: Will receive a single, more powerful radiation treatment of 20 Gy. Participants in this study will: Receive a single, one-time, highly-focused radiation treatment (SSRS) to the spinal tumor. Attend regular follow-up visits at the clinic for checkups and imaging scans (like MRI). Complete questionnaires about their pain levels and quality of life during these visits.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with a histologic diagnosis of non-hematopoietic malignancy

• Radiographic evidence of localized spine metastases without leptomeningeal involvement or intramedullary lesion

• Maximum four separate sites with a maximal involvement of two continuous vertebral levels

• Patients do not have prior radiotherapy to the index spine(s)

• Age ≥ 18 years

• Karnofsky performance status (KPS) ≥ 60%.

• Life expectancy ≥ 12 months.

• Women of childbearing potential and male participants must practice adequate contraception

• Patients must be able to comply with the study protocol and follow-up schedules and provide study-specific informed consent

Locations
Other Locations
Taiwan
National Taiwan University Cancer Center
RECRUITING
Taipei
National Taiwan University Hospital
RECRUITING
Taipei
Contact Information
Primary
Feng-Ming Hsu, M.D., Ph.D
hsufengming@ntuh.gov.tw
886-2-23123456
Time Frame
Start Date: 2025-06
Estimated Completion Date: 2035-06
Participants
Target number of participants: 196
Treatments
Active_comparator: Standard Dose Spine Stereotactic Radiosurgery
Participants randomized to this arm will receive Spine Stereotactic Radiosurgery (SSRS) delivered at a dose of 16 Gray (Gy) in a single treatment session.
Experimental: High Dose Spine Stereotactic Radiosurgery
Participants randomized to this arm will receive Spine Stereotactic Radiosurgery (SSRS) delivered at a higher dose of 20 Gray (Gy) in a single treatment session.
Related Therapeutic Areas
Sponsors
Collaborators: National Taiwan University Hospital, Yun-Lin Branch, National Taiwan University Hospital Hsin-Chu Branch, National Taiwan University
Leads: National Taiwan University Hospital

This content was sourced from clinicaltrials.gov