Randomized Study of Stereotactic Body Radiotherapy vs. Conventional Radiation for Spine Metastasis

Phase 2

Terminated

Conditions: Primary Tumor
Metastatic Cancer

Interventions: Radiation: Radiosurgery/SBRT
Radiation: External Beam Radiation Therapy

Registration Number: NCT01525745

Lead Sponsor: Beth Israel Deaconess Medical Center

Brief Summary: The purpose of this study is to determine how effective SBRT is compared to traditional radiation in treating the cancer that has spread to your spine and is causing pain. SBRT is delivered at a higher dose for a shorter period of time when compared to standard radiation therapy and the aim is to see if there will be an improvement both in pain control and your cancer It is not known whether SBRT is better or worse than current standard therapy. If you are selected to receive the experimental treatment in this research study, SBRT uses highly focused x-rays that deliver a single high dose to a specific area of the spine compared to conventional standard radiation over a period of 10 days which has been the standard proven treatment to help your condition. The investigators will also determine which treatment provides the most rapid pain relief with the least side effects. It is possible that SBRT may not be better or could be more toxic. The investigators will conduct quality of life assessments and pain scale index to assess how you are feeling once you have had the intervention.

Detailed Description: Randomization means that you are put into a group by chance. It is like flipping a coin. Neither you nor the research doctor will choose what group you will be in.

You will have a 2 to 1 chance of being placed in the SBRT to standard radiation group. Since SBRT is the newer treatment being tested, we would like to include more patients in this group.

Treatment Procedures:

SBRT: You may receive one, three or five SBRT treatments depending on the extent of your cancer. During each treatment you will be assessed by a nurse and a physician for a physical and neurological assessment. The treatment itself would last approximately I hour where you will be lying on a treatment table. Prior to each treatment you will have a physical and neurological assessment by a physician. Standard Radiation: You will receive ten consecutive working days of standard radiation. While each treatment lasts five to ten minutes, the entire visit may last up to thirty minutes. During the treatment you will be lying on a treatment table. Once per week you will have a physical and neurological assessment by your treating physician After the final treatment of the study therapy: We would like to keep track of your medical condition for at least 12 months after you receive treatment. We would like to do this by having you come in to the clinic at months 1, 3, 6, 12 and 24 months after treatment\*. At these visits we will be looking for the same information as during the screening time frame. This includes:

* A history and physical from you

* A Performance Status of how you are able to carry on with your usual activities.

* A Pain scale questionnaire called the Numerical Rating Pain Scale(NRPS) that asks to explain your pain symptoms on a 0-10 scale

* 3 Quality Of Life (QOL) Assessments described below:

* Functional Assessment of Cancer Therapy-General (FACT-G)

* The Brief Pain Inventory (BPI)

* The EuroQOL (EQ-5D)

* An assessment of your tumor by MRI (Magnetic Resonance Imaging)

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 6

Inclusion Criteria

Histologically confirmed primary tumor or metastatic cancer with radiological diagnosis of spine metastasis
The patient must have localized spine metastasis from the C1 to L5 levels by a screening imaging study
Zubrod Performance Status 0-2
History/physical examination within 2 weeks prior to registration
Negative pregnancy test within 2 weeks prior to registration for women of childbearing potential
Women of childbearing potential and male participants who are sexually active must agree to use a medically effective contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation.
MRI of the involved spine within 4 weeks prior to registration to determine the extent of the spine involvement
Numerical Rating Pain Scale within 1 week prior to registration; the patient must have a score on the Scale of >5 for at least one of the planned sites for spine radiosurgery. Patients taking medication for pain at the time of registration are eligible.
Neurological examination within 1 week prior to registration to rule out rapid neurologic decline

Exclusion Criteria

Histology of myeloma, lymphoma or germ cell tumors.
Non-ambulatory patients
Spine instability due to a compression fracture
> 50% loss of vertebral body height
Frank spinal cord displacement or epidural involvement with> 25% encirclement of cord or >25% spinal canal involvement.
Prior radiation to the index spine
Patients for whom an MRI of the spine is medically contraindicated
Uncontrolled intercurrent illness

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Radiosurgery/SBRT	Radiosurgery/SBRT	Radiosurgery/SBRT
External Beam Radiation Therapy	External Beam Radiation Therapy	External Beam Radiation Therapy

Primary Outcome Measures

Name	Time	Method
Pain Control as Measured by NPRS	2 years	Determine if image-guided radiosurgery/SBRT improves pain control as measured by NPRS as compared to conventional external beam radiotherapy

Secondary Outcome Measures

Name	Time	Method
Duration of Pain Response	2 years	Determine if image-guided radiosurgery/SBRT improves duration of pain as compared to conventional external beam radiotherapy
Long Term Effects of Image-guided Radiosurgery/SBRT	2 years	Long term effects of image-guided radiosurgery/SBRT on the vertevral bone and spinal cord
Quality of Life	2 years	Evaluate potential benefit of image-guided radiosurgery/SBRT on change in and overall quality of life as measured by FACT-G, BPI and EQ-5D
Survival	2 years	Progrsesion Free and Overall Survival

Trial Locations

Locations (3): Beth Israel Deacness Medical Center
🇺🇸
Boston, Massachusetts, United States
Brigham and Women's Hospital
🇺🇸
Boston, Massachusetts, United States
Dana-Farber Cancer Institute
🇺🇸
Boston, Massachusetts, United States