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Radiation

SBRT boost for Cauda Equina Syndrome (CRUSSH Trial)

N/A
Waitlist Available
Research Sponsored by Juravinski Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks, 12 weeks, 6 months
Awards & highlights
No Placebo-Only Group

Summary

Spinal cord compression (SCC) is a devastating complication of advanced malignancy, and can cause significant deterioration in function and quality of life (QoL). The goal of treatment is to improve functional status and symptoms, but the optimal treatment regimen for these patients has not been thoroughly established. Many patients with SCC present with uncontrolled systemic disease and poor performance status, and are not eligible for standard surgical resection. They are generally treated with 3D conformal palliative RT (3DCRT) alone, however recent trials suggest that less than 70% of patients are ambulatory, that the re-establishment of ambulation in non-ambulatory patients is poor, and the duration of improvement is guarded with radiotherapy alone. Recently, stereotactic body radiotherapy (SBRT) used alone or after previous radiotherapy to treat spinal metastasis has demonstrated superior results in pain control, tumour response and durability. SBRT requires time for careful planning, and many patients with neurologic symptoms must be treated immediately to prevent progression. Therefore the role of SBRT is still unclear in this patient population, although it seems to be a potential alternative to surgical decompression in patient not suitable for surgery. The investigators propose a feasibility study to investigate the potential benefits of dose escalation with a sequential SBRT boost to urgent 3D CRT in the setting of SCC. This regimen will allow inoperable patients to receive urgent 3DCRT while simultaneously creating the opportunity for superior outcomes with SBRT. The investigators also aim to characterize the effect on motor function and ambulation, pain and QoL. This study could stimulate further multi-center randomized trials in this area, improve motor function and patient-reported QoL, and contribute to improving oncology care in Canada in a meaningful way.

Eligible Conditions
  • Cauda Equina Syndrome
  • Spinal Cord Compression
  • Stereotactic Body Radiotherapy

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks, 12 weeks, 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 weeks, 12 weeks, 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Feasibility of accrual
Secondary study objectives
Bone metastasis- specific Quality of Life
Local Control
Motor Function Description
+4 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: SBRT boostExperimental Treatment1 Intervention
Standard radiotherapy (3D conformal, urgent palliative radiotherapy) plus stereotactic body radiotherapy (SBRT) boost

Find a Location

Who is running the clinical trial?

Juravinski Cancer CenterLead Sponsor
13 Previous Clinical Trials
2,315 Total Patients Enrolled
Hamilton Health Sciences CorporationOTHER
377 Previous Clinical Trials
340,370 Total Patients Enrolled
Juravinski Cancer Centre FoundationOTHER
12 Previous Clinical Trials
1,923 Total Patients Enrolled
~4 spots leftby Nov 2025