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

Randomized Ph II Study of Stereotactic Body Radiotherapy (SBRT) Versus Conventional Radiation for Spine Metastasis

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01525745
Enrollment
6
Registered
2012-02-03
Start date
2012-01-31
Completion date
2014-01-31
Last updated
2017-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic Cancer, Primary Tumor

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)

Interventions

1, 3 or 5 SBRT treatments

RADIATIONExternal Beam Radiation Therapy

10 consecutive days of standard radiation

Sponsors

Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pain Control as Measured by NPRS2 yearsDetermine if image-guided radiosurgery/SBRT improves pain control as measured by NPRS as compared to conventional external beam radiotherapy

Secondary

MeasureTime frameDescription
Duration of Pain Response2 yearsDetermine if image-guided radiosurgery/SBRT improves duration of pain as compared to conventional external beam radiotherapy
Quality of Life2 yearsEvaluate potential benefit of image-guided radiosurgery/SBRT on change in and overall quality of life as measured by FACT-G, BPI and EQ-5D
Long Term Effects of Image-guided Radiosurgery/SBRT2 yearsLong term effects of image-guided radiosurgery/SBRT on the vertevral bone and spinal cord
Survival2 yearsProgrsesion Free and Overall Survival

Countries

United States

Participant flow

Recruitment details

all participants were enrolled in the RadOnc clinic at BIDMC

Participants by arm

ArmCount
A/Radiosurgery-SBRT
Radiosurgery/SBRT: 1, 3 or 5 SBRT treatments
4
B/External Beam Radiation Therapy
External Beam Radiation Therapy: 10 consecutive days of standard radiation
2
Total6

Baseline characteristics

CharacteristicA/Radiosurgery-SBRTB/External Beam Radiation TherapyTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
2 Participants1 Participants3 Participants
Age, Categorical
Between 18 and 65 years
2 Participants1 Participants3 Participants
Region of Enrollment
United States
4 participants2 participants6 participants
Sex: Female, Male
Female
2 Participants1 Participants3 Participants
Sex: Female, Male
Male
2 Participants1 Participants3 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 40 / 2
serious
Total, serious adverse events
0 / 40 / 2

Outcome results

Primary

Pain Control as Measured by NPRS

Determine if image-guided radiosurgery/SBRT improves pain control as measured by NPRS as compared to conventional external beam radiotherapy

Time frame: 2 years

Population: study was terminated by the local IRB due to slow accrual. 1 participant withdrew consent and 1 participant did not complete the assigned arm treatment per protocol and then removed from study. left with 4 participants and data were not collected for any participants therefore no analysis has been done.

Secondary

Duration of Pain Response

Determine if image-guided radiosurgery/SBRT improves duration of pain as compared to conventional external beam radiotherapy

Time frame: 2 years

Population: data not collected, therefore no analysis done

Secondary

Long Term Effects of Image-guided Radiosurgery/SBRT

Long term effects of image-guided radiosurgery/SBRT on the vertevral bone and spinal cord

Time frame: 2 years

Population: data not collected, therefore no analysis done

Secondary

Quality of Life

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

Time frame: 2 years

Population: data not collected, therefore no analysis done

Secondary

Survival

Progrsesion Free and Overall Survival

Time frame: 2 years

Population: data not collected, therefore no analysis done

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026