Prophylactic Radiotherapy of MInimally Symptomatic Spinal Disease
ConditionSpine Metastases
Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorBaptist Health South Florida
About this trial
Early palliative care has been shown to improve the quality of life and even survival for patients with metastatic cancer. More and more supportive oncology teams in cancer centers now advocate for early integration of radiation therapy (RT) in a patient's palliative management course. While multiple randomized studies have evaluated the efficacy of different RT regimens in the treatment of symptomatic bone lesions, few studies have examined the impact of early, upfront RT for asymptomatic or minimally symptomatic (non- opioid dependent) spine metastases and its efficacy in preventing skeletal-related events (SREs). Since the pathophysiology of spinal metastatic disease is distinct from other bony metastatic disease, the proposed trial seeks to understand whether it is beneficial to patients with minimally symptomatic disease to undergo upfront RT to reduce the risks of SREs and their sequelae, including hospitalizations.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Histologically-confirmed solid tumor malignancy with greater than 5 sites of metastatic disease detected on cross-sectional imaging.
Bulkiest sites of spinal osseous disease ≥ 2cm,
Disease at junctional levels, including the thoracic apex (Occiput to C2, C7-T1, T12-L2, and L5- S1)
Disease with posterior element involvement, including interspinous, unilateral, or bilateral facet joints.
Disqualifiers
Previous RT to the intended treatment site that precludes developing a treatment plan that respects normal tissue tolerances.
Serious medical co-morbidities precluding RT.
Pregnant or lactating women.
Target lesion(s) is/are complicated bone metastases that include clinical or radiological evidence of spinal cord compression or impending pathological fracture.
Trial design
Design model
Parallel
Treatments tested in this trial
Prophylactic Radiotherapy
RadiationRadiation therapy will be delivered according to department standards. For this protocol, total dose and dose fractionation may be delivered at the discretion of the treating radiation oncologist according to department standards. All techniques including conventional, three-dimensional conformal radiation therapy (3D-CRT), intensity-modulated radiation therapy (IMRT), and stereotactic radiosurgery/stereotactic body radiation therapy (SRS/SBRT) techniques may be used. Image guidance at the time of treatment delivery to verify patient positioning may be chosen at the discretion of the treating radiation oncologist according to department standards.
Standard of care systemic therapy
DrugStandard of care systemic therapy, including chemotherapeutics, targeted therapies, immunomodulatory agents, and hormonal therapies will be delivered at the discretion of the treating medical oncologist. Patients may receive systemic therapy concurrently and there are no restrictions on initiation of systemic agents after radiotherapy including immunotherapy and hormonal therapy, the timing of which will be determined by a consensus between the treating medical and radiation oncologists.
Treatment groups
74 Participants
are divided into 2 treatment groupsGroup A: Standard of Care Systemic Therapy or SurveillanceActive comparator 1 intervention
Group B: Prophylactic Radiation TherapyExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Number of patients who have skeletal-related events (SREs)
Number of skeletal related events (SREs), which will be defined as pathological fractures, spinal cord compression, or interventions (palliative RT, interventional procedures, or spine surgery)
Time frame
1 yearSecondary outcomes
1
Number of skeletal-related event (SRE) hospitalizations
Number of hospitalizations attributed to skeletal-related events (SREs)
Time frame
1 year2
Pain-related quality of life
Pain-related quality of life using the Brief Pain Inventory (BPI) form. The BPI is a 17-item patient self-rating scale assessing demographic data, use of medications, as well as the sensory and reactive components of pain. The scale is from 0-10, and there are breakpoints between scores of 4 and 5 and between 6 and 7, indicating that mild pain correlates with scores of 1-4, moderate pain with 5-6, and severe pain with scores of 7-10.
Time frame
3 months, 6 months, and 12 months, optionally within 1 week of a skeletal-related event (SRE)3
Health care utilities and quality of life
Health care utilities and quality of life using the EuroQol Group EQ-5D-5L form and FACT-G questionnaires. It has been developed to generate a generic cardinal index of health, thus giving it considerable potential for future use in economic evaluation. The EQ-5D-5L is a two-part, patient-completed questionnaire. The first part consists of 5 items covering 5 dimensions including: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension can be graded on 3 levels including: 1=no problems; 2= moderate problems; and 3=extreme problems. The second component is the visual analog scale, where the participant rates their own overall health on a scale of 0 (worst health) to 100 (best health).
Time frame
3 months, 6 months, and 12 months, optionally within 1 week of a skeletal-related event (SRE)4
Pain-free survival (PFS)
Pain-free survival (PFS) is defined as the time from study entry to until the start of opioid use or until death.
Time frame
Until 1 yearSponsors and contacts
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Source ClinicalTrials.gov