Spine Radiosurgery for Symptomatic Metastatic Neoplasms

Case Comprehensive Cancer Center (Case CCC)

Status and phase: Active, not recruiting; Phase 2

Conditions: Metastatic Neoplasm; Metastatic Neoplasm to the Spine

Treatments: Radiation: Spine radiosurgery/stereotactic body radiation therapy high dose; Radiation: Spine radiosurgery/stereotactic body radiation therapy standard dose; Radiation: Conventional external beam radiation therapy dose (EBRT)

Study type: Interventional

Funder types: Other

Identifiers

NCT05617716

CASE4322

Details and patient eligibility

About

The purpose of this study is to compare three types of radiation therapy for cancer that has spread to the spine. The two types of radiation therapy used in this trial are External Beam Radiation Therapy (EBRT) and Stereotactic Body Radiation Therapy (SBRT). EBRT delivers tightly targeted radiation beams from outside the body. SBRT is a specialized type of radiation therapy that allows high doses of radiation to small targets. This study will include standard dose SBRT and higher dose SBRT. Each participant will be randomly assigned to either EBRT, standard dose SBRT, or higher dose SBRT.

Full description

Metastatic spine cancer incidence is increasing; the primary treatment is radiation therapy. Metastatic spine disease has been historically treated with external beam radiation therapy (EBRT) with conventional fractionation, yielding relatively limited durability in pain control. The increased lifespan of patients with metastatic cancer has resulted in an increase in the incidence of spine metastases, which has led to a need for more durable treatment results. Stereotactic radiosurgery (SRS)/Stereotactic body radiation therapy (SBRT) of the spine has exponentially increased, with the theoretical advantages of higher tumoricidal dose and more rapid fall off between tumor and surrounding normal tissue compared with EBRT. The goal of this study is to compare three types of radiation therapy to draw conclusions on what is an effective treatment to reduce pain and increase pain freedom rates.

Enrollment: 16 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participant must have histologic confirmation of malignancy. Spinal metastatic disease must be confirmed by imaging.
• Participant must have received no prior therapies for this disease. Prior therapy includes previous radiation therapy encompassing the anatomic site to be treated with spine SBRT. This includes any previous radiation therapy where the treatment field overlaps with the anatomic site to be treated with spine SBRT (even if that previous radiation therapy was not for treatment of spinal disease). Systemic radiation therapy for metastatic disease such as Pluvicto also counts as previous radiation therapy.
• Age >18 years. This study requires informed consent by the participant; as children are not able to perform this without parental approval, Participant < age 18 are excluded from this study.
• Life expectancy of≥ 3 months, in the opinion of and as documented by the investigator.
• Participant must have a worst pain score < 2 of 10 according to the Brief Pain Inventory
• Participant must have no intention of changing pain medications on the first day of SBRT
• Participant must have a Spinal Instability score (SINS) ≤ 12
• Participant must be a spine SBRT candidate per Radiation Oncology
• Participant must have the ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

• Participant receiving any other investigational agents.
• Participant with prognosis less than 3 months will be excluded from this clinical trial because of their poor prognosis and decreased likelihood to meet the primary endpoint
• Participant with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant or nursing Participant are excluded due to toxicity of radiation therapy.
• Participant is unable to receive MRI of the spine
• Participant has a Spinal Instability in Neoplasia score (SINS) ≥ 12
• Participant has received previous stereotactic radiosurgery where the 50% isodose line overlaps with current treatment field
• Participant has more than 3 consecutive vertebral bodies in the SBRT treatment volume
• Participant is not an SBRT candidate per radiation oncology discretion
• Participant has a known primary and has an estimated median survival≤ 3 months
• Participant has an unknown primary
• Participant has a Brief Pain Inventory score > 2
• Participant has received previous radiation therapy involving the intended SBRT treatment field
• Participant has received previous spinal surgical procedure involving the SBRT target volume. Biopsy is not considered a previous spinal surgical procedure.
• Participant has neurological deficits from malignant cauda equina compression or epidural spinal cord compression

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

16 participants in 3 patient groups

Standard dose SBRT

Experimental group

Description:

Participants will undergo standard dose Stereotactic Body Radiation Therapy

Treatment:

Radiation: Spine radiosurgery/stereotactic body radiation therapy standard dose

High dose SBRT

Experimental group

Description:

Participants will undergo high dose Stereotactic Body Radiation Therapy

Treatment:

Radiation: Spine radiosurgery/stereotactic body radiation therapy high dose

Conventional EBRT

Experimental group

Description:

Participants will undergo External Beam Radiation Therapy

Treatment:

Radiation: Conventional external beam radiation therapy dose (EBRT)