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Stereotactic Body Radiotherapy Boost After Palliative Radiotherapy for Spinal Cord Compression (CRUSSH)

Primary Purpose

Spinal Cord Compression, Cauda Equina Syndrome, Stereotactic Body Radiotherapy

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
3D CRT plus SBRT boost
Sponsored by
Juravinski Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Compression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of metastatic malignancy (radiologic or pathologic)
  2. Evidence of disease in vertebral body with epidural component such that Bilsky radiologic score is 1c-2 on MRI (abuts spinal cord without cord compression (1c), or spinal cord compression but with visible CSF (2)
  3. Motor function (MF) of 3 or greater

Exclusion Criteria:

  1. Surgical candidate
  2. Instability of vertebral bodies with or without bony retropulsion requiring surgical intervention or hardware placement
  3. Previous radiotherapy course to same region of spine with overlapping fields (prior to phase I course) at discretion of treating radiation oncologist
  4. No CT or MRI within previous 3 months
  5. Life expectancy estimated <3 months
  6. Performance status KPS<40
  7. On active chemotherapy or targeted therapy or immunotherapy (must be stopped for at least one week prior to and following)
  8. Pregnant or lactating
  9. Contraindications to radiotherapy (eg. active autoimmune disease requiring medication)
  10. Inability to lie flat comfortably for at least 20 minutes
  11. Age < 18

Sites / Locations

  • Juravinski Cancer CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SBRT boost

Arm Description

Standard radiotherapy (3D conformal, urgent palliative radiotherapy) plus stereotactic body radiotherapy (SBRT) boost

Outcomes

Primary Outcome Measures

Feasibility of accrual
Success determined by accrual of 30 patients with SBRT boost is planned and delivered to 80% of these

Secondary Outcome Measures

Motor Function Description:
Motor strength evaluated by 8 point scale (0= Complete paraplegia, 1= Palpable or visible muscle contractions, 2= Active movement of the leg without gravity, 3= Active movement of the leg against gravity, 4= Active movement againt mild resistance, 5= Active movement against intermediate resistance, 6= Active movement against strong resistance, 7= Normal strength)
Overall Quality of Life (QoL)
Change in total QoL score over time per European Organization for Research and Treatment of Cancer Quality of Life Questionnaire core 30 (EORTC QLQ-c30)
Pain Response
Change in level of pain over time on 10 point scale with 0 meaning no pain and 10 meaning severe pain (patient-reported)
Local Control
Assessment of tumor volume (maximum size in 3 dimension) by Magnetic Resonance Imaging (MRI)
Toxicity
Treatment-related toxicity graded by Common Terminology for Adverse Events (CTCAE 4.03)
Overall Survival
Survival time from first radiotherapy treatment (3D CRT) in days
Bone metastasis- specific Quality of Life
Change in total QoL score over time per European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Bone Metastasis-22 (EORTC QLQ BM-22)

Full Information

First Posted
April 24, 2018
Last Updated
January 27, 2020
Sponsor
Juravinski Cancer Center
Collaborators
Hamilton Health Sciences Corporation, Juravinski Cancer Centre Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03529708
Brief Title
Stereotactic Body Radiotherapy Boost After Palliative Radiotherapy for Spinal Cord Compression
Acronym
CRUSSH
Official Title
Stereotactic Body Radiotherapy (SBRT) Boost Following Urgent 3D Conformal Radiotherapy in the Treatment of Metastatic Epidural Spinal Cord Compression (SCC): A Phase I Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
June 1, 2020 (Anticipated)
Study Completion Date
December 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Juravinski Cancer Center
Collaborators
Hamilton Health Sciences Corporation, Juravinski Cancer Centre Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Compression, Cauda Equina Syndrome, Stereotactic Body Radiotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single arm pilot study of standard of care 3D conformal radiotherapy plus Stereotactic body radiotherapy (SBRT) boost
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
SBRT boost
Arm Type
Experimental
Arm Description
Standard radiotherapy (3D conformal, urgent palliative radiotherapy) plus stereotactic body radiotherapy (SBRT) boost
Intervention Type
Radiation
Intervention Name(s)
3D CRT plus SBRT boost
Intervention Description
Patients will receive urgent standard 3D conformal radiotherapy (3D CRT) of plus stereotactic boost to tumor causing spinal cord compression (SCC). Initial dose for 3D CRT will be either 8Gy in 1 fraction or 20Gy in 5 fractions, with SBRT boost dose15Gy in 2 fractions of 12Gy in 2 fractions (depending on 8Gy/1 or 20Gy/5 initial RT dose respectively), delivered within three weeks of first treatment.
Primary Outcome Measure Information:
Title
Feasibility of accrual
Description
Success determined by accrual of 30 patients with SBRT boost is planned and delivered to 80% of these
Time Frame
up to 12 months
Secondary Outcome Measure Information:
Title
Motor Function Description:
Description
Motor strength evaluated by 8 point scale (0= Complete paraplegia, 1= Palpable or visible muscle contractions, 2= Active movement of the leg without gravity, 3= Active movement of the leg against gravity, 4= Active movement againt mild resistance, 5= Active movement against intermediate resistance, 6= Active movement against strong resistance, 7= Normal strength)
Time Frame
4 weeks (primary), 12 weeks, 6 months
Title
Overall Quality of Life (QoL)
Description
Change in total QoL score over time per European Organization for Research and Treatment of Cancer Quality of Life Questionnaire core 30 (EORTC QLQ-c30)
Time Frame
4 weeks, 12 weeks, 6 months
Title
Pain Response
Description
Change in level of pain over time on 10 point scale with 0 meaning no pain and 10 meaning severe pain (patient-reported)
Time Frame
4 weeks, 12 weeks, 6 months
Title
Local Control
Description
Assessment of tumor volume (maximum size in 3 dimension) by Magnetic Resonance Imaging (MRI)
Time Frame
12 weeks, 6 months
Title
Toxicity
Description
Treatment-related toxicity graded by Common Terminology for Adverse Events (CTCAE 4.03)
Time Frame
4 weeks, 12 weeks, 6 months
Title
Overall Survival
Description
Survival time from first radiotherapy treatment (3D CRT) in days
Time Frame
4 weeks, 12 weeks, 6 months
Title
Bone metastasis- specific Quality of Life
Description
Change in total QoL score over time per European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Bone Metastasis-22 (EORTC QLQ BM-22)
Time Frame
4 weeks, 12 weeks, 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of metastatic malignancy (radiologic or pathologic) Evidence of disease in vertebral body with epidural component such that Bilsky radiologic score is 1c-2 on MRI (abuts spinal cord without cord compression (1c), or spinal cord compression but with visible CSF (2) Motor function (MF) of 3 or greater Exclusion Criteria: Surgical candidate Instability of vertebral bodies with or without bony retropulsion requiring surgical intervention or hardware placement Previous radiotherapy course to same region of spine with overlapping fields (prior to phase I course) at discretion of treating radiation oncologist No CT or MRI within previous 3 months Life expectancy estimated <3 months Performance status KPS<40 On active chemotherapy or targeted therapy or immunotherapy (must be stopped for at least one week prior to and following) Pregnant or lactating Contraindications to radiotherapy (eg. active autoimmune disease requiring medication) Inability to lie flat comfortably for at least 20 minutes Age < 18
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elysia K Donovan, MD,FRCPC
Phone
9053879495
Email
donovane@hhsc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Shelley Chambers, MA
Phone
9053879495
Facility Information:
Facility Name
Juravinski Cancer Center
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V1C5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kara L Schnarr

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33208170
Citation
Donovan EK, Greenspoon J, Schnarr KL, Whelan TJ, Wright JR, Hann C, Whitton A, Chow T, Parpia S, Swaminath A. A pilot study of stereotactic boost for malignant epidural spinal cord compression: clinical significance and initial dosimetric evaluation. Radiat Oncol. 2020 Nov 18;15(1):267. doi: 10.1186/s13014-020-01710-4.
Results Reference
derived

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Stereotactic Body Radiotherapy Boost After Palliative Radiotherapy for Spinal Cord Compression

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