Stereotactic Body Radiotherapy for Osseous Low Alpha-Beta Resistant Metastases for Pain Relief (SOLAR-P)
Primary Purpose
Bone Metastases, Prostate Cancer, Breast Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
SBRT
Sponsored by
About this trial
This is an interventional treatment trial for Bone Metastases focused on measuring SOLAR-P, SBRT, Bone metastases, stereotactic, pain relief, quality of life, palliation, low alpha beta, radioresistant
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of prostate cancer, renal cell carcinoma, or melanoma
- Radiographic evidence of bone metastases requiring treatment for pain
- Brief Pain Inventory score of ≥ 2
Exclusion Criteria:
- Spinal lesions
- Severe or progressive neurological deficit
- Impending or existing pathological fracture
- Bone metastasis in a previously irradiated site
- Active systemic therapy
- >5 lesions requiring treatment
- Lesions >5 cm in largest diameter
- Life expectancy < 3 months
- Age < 18
- Karnofsky Performance Status < 50
- Unable to provide informed consent
Sites / Locations
- Juravinski Cancer CentreRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Stereotactic Body Radiotherapy
Arm Description
High dose SBRT to lesion(s) of interest.
Outcomes
Primary Outcome Measures
Overall Pain Response
Assessed using the Brief Pain Inventory
Secondary Outcome Measures
Overall Pain Response
Assessed using the Brief Pain Inventory
Acute Toxicity
According to the Common Terminology Criteria for Adverse Events 5.0
Late Toxicity
According to the Common Terminology Criteria for Adverse Events 5.0
Patient-reported Quality of Life
Assessed by EORTC quality of life questionnaires
Local Control
Assessed radiographically
Rate of Reirradiation/Salvage Surgery
Due to instability or symptomatic progression
Full Information
NCT ID
NCT04177056
First Posted
November 14, 2019
Last Updated
July 26, 2021
Sponsor
Hamilton Health Sciences Corporation
Collaborators
Juravinski Cancer Centre Foundation
1. Study Identification
Unique Protocol Identification Number
NCT04177056
Brief Title
Stereotactic Body Radiotherapy for Osseous Low Alpha-Beta Resistant Metastases for Pain Relief
Acronym
SOLAR-P
Official Title
Stereotactic Body Radiotherapy for Osseous Low Alpha-Beta Resistant Metastases for Pain Relief
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 4, 2020 (Actual)
Primary Completion Date
March 1, 2022 (Anticipated)
Study Completion Date
January 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamilton Health Sciences Corporation
Collaborators
Juravinski Cancer Centre Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Radiation therapy has been shown to be very effective at relieving pain caused by bone metastases. However, certain types of cancers such as prostate, breast, kidney, and melanoma can have resistance to radiation, making treatment less successful. Stereotactic body radiotherapy (SBRT) is a newer form of focused treatment that gives higher doses of radiation without damage to surrounding organs. It often is used to help control and cure disease, but less commonly as a way to palliate and treat symptoms. This study is looking at using SBRT for the purposes of improving pain caused by bone metastases in prostate cancer, breast cancer, kidney cancer, and melanoma patients. It is theorized that the higher levels of radiation may be able to combat the resistance some tumour cells have to radiotherapy and provide improved pain response to treatment. The investigators are looking to show that SBRT has a role in helping this group of patients deal with painful bone lesions from their cancer without increasing side effects and toxicity from the radiation treatment.
Detailed Description
Stereotactic body radiotherapy (SBRT) has shown promising early results in the management of bone metastases. However, there is a paucity of prospective data studying the use of SBRT for bone metastases originating from low alpha-beta tumors, with systematic reporting of changes in pain scores and analgesia use over time. The vast majority data looking at SBRT in bone lesions focuses on local control and survival, rather than more tangible outcomes in a palliative population including symptomatic control, durability of response, and patient reported quality of life; a component that is understudied in this group despite its tremendous value. Furthermore, SBRT for bone metastases has yet to become common practice given the limited evidence for its efficacy and uncertainty in regards to toxicity.
The current study proposes an investigation of the potential benefits of SBRT for symptomatic bone metastases in patients with prostate cancer, breast cancer, renal cell carcinoma, melanoma, and sarcoma. The investigators look to conduct a prospective cohort study that is adequately powered to analyse efficacy in alleviating pain from bone lesions and compare this to well-established rates in literature for conventionally fractionated palliative RT. Furthermore, this study will assess the tolerability of this modality, toxicity rates, and effect on quality of life. If the results show that SBRT has a significant benefit on this population, the goal would be to pursue a larger randomized trial to confirm the findings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Metastases, Prostate Cancer, Breast Cancer, Renal Cell Carcinoma, Melanoma
Keywords
SOLAR-P, SBRT, Bone metastases, stereotactic, pain relief, quality of life, palliation, low alpha beta, radioresistant
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Stereotactic Body Radiotherapy
Arm Type
Experimental
Arm Description
High dose SBRT to lesion(s) of interest.
Intervention Type
Radiation
Intervention Name(s)
SBRT
Intervention Description
Patients will received a single fraction of 15-20 Gy to bone metastases causing pain. Planning and delivery will be conducted using a volumetric modulated arc therapy (VMAT) approach on the Varian TrueBeam platform. Patients will be CT simulated, with vac-lock immobilization. Use of 4-dimensional CT will be dependent on the area being treated. Daily image guidance will be performed using cone beam CT aligning to relevant bony anatomy.
Primary Outcome Measure Information:
Title
Overall Pain Response
Description
Assessed using the Brief Pain Inventory
Time Frame
3 months after treatment
Secondary Outcome Measure Information:
Title
Overall Pain Response
Description
Assessed using the Brief Pain Inventory
Time Frame
6 months after treatment
Title
Acute Toxicity
Description
According to the Common Terminology Criteria for Adverse Events 5.0
Time Frame
3 months or less
Title
Late Toxicity
Description
According to the Common Terminology Criteria for Adverse Events 5.0
Time Frame
greater than 3 months
Title
Patient-reported Quality of Life
Description
Assessed by EORTC quality of life questionnaires
Time Frame
1 month, 3 months, and 6 months
Title
Local Control
Description
Assessed radiographically
Time Frame
up to 1 year
Title
Rate of Reirradiation/Salvage Surgery
Description
Due to instability or symptomatic progression
Time Frame
up to 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of prostate cancer, renal cell carcinoma, or melanoma
Radiographic evidence of bone metastases requiring treatment for pain
Brief Pain Inventory score of ≥ 2
Exclusion Criteria:
Spinal lesions
Severe or progressive neurological deficit
Impending or existing pathological fracture
Bone metastasis in a previously irradiated site
Active systemic therapy
>5 lesions requiring treatment
Lesions >5 cm in largest diameter
Life expectancy < 3 months
Age < 18
Karnofsky Performance Status < 50
Unable to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephan Tran, MD
Phone
905-387-9711
Ext
63123
Email
transt@hhsc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Eric K Nguyen, MD
Phone
905-387-9711
Ext
63123
Email
eric.nguyen@medportal.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anand Swaminath, MD
Organizational Affiliation
Hamilton Health Sciences Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Juravinski Cancer Centre
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V 5C2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anand Swaminath, MD
Phone
905-387-9711
Email
swaminath@hhsc.ca
12. IPD Sharing Statement
Citations:
PubMed Identifier
34479581
Citation
Nguyen EK, Quan K, Parpia S, Tran S, Swaminath A. Stereotactic body radiotherapy for osseous low alpha-beta resistant metastases for pain relief-SOLAR-P. Radiat Oncol. 2021 Sep 3;16(1):170. doi: 10.1186/s13014-021-01897-0.
Results Reference
derived
Learn more about this trial
Stereotactic Body Radiotherapy for Osseous Low Alpha-Beta Resistant Metastases for Pain Relief
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