Spine SABR - Dose-escalated Stereotactic Ablative Body Radiotherapy (SABR) for Solid Tumour Spine Metastases (Spine-SABR)

Cancer Trials Ireland

Status and phase: Enrolling; Phase 2; Phase 1

Conditions: Solid Tumor Spine Metastases

Treatments: Radiation: Radiation: image guided dose escalated SABR using a simultaneous integrated boost (SIB)

Study type: Interventional

Funder types: NETWORK

Identifiers

NCT06078813

CTRIAL-IE 20-03

Details and patient eligibility

About

This study will look at treatment for patients that have already been diagnosed with cancer, but develop a new tumor(s) in the spine. Patients who are not recommended for surgery are usually treated with 5-10 sessions of radiotherapy to manage symptoms. For patients with a longer life expectancy (>6 months), it is better to give a higher dose of treatment to potentially improve the duration of pain relief, cancer control and potentially survival. Higher doses of radiotherapy, however, may also cause worse toxicity and side effects. This study will look at delivering higher doses of radiation in 2 sessions rather than 5-10, using a more modern, targeted technique called image-guided Stereotactic Ablative Body Radiotherapy (SABR). This method requires special equipment and expertise compared to the traditional radiotherapy and this has limited availability in Ireland. This study aims to find out the highest dose that is safe to be given to patients and carefully examine the side effects. These results will help create national and international guidelines to benefit all cancer patients. Patients will be monitored closely during treatment and for 2 years afterwards. Patients have been involved in developing the treatment protocol and the patient information leaflet. Patients will also be asked to fill in quality of life (QOL) questionnaires at certain timepoints during the study. It is anticipated that this study will support the delivery of high quality SABR to all cancer patients in Ireland, resulting in potentially better quality of life, symptom and tumor control.

Enrollment: 126 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Written informed consent obtained prior to any study-related procedures

2. ≥ 18 years of age

3. Life expectancy > 6 months

4. ECOG (Eastern Cooperative Oncology Group) performance status (PS) 0-2

5. Histological diagnosis of malignant primary disease (excluding haematologic, seminomatous or small cell subtype)

6. Diagnosis of oligometastatic disease (OMD) or oligoprogressive disease (OPD) defined as:

   1. OMD where there are 1 to 5 metastatic lesions, with a controlled primary tumor being optional, but where all metastatic sites must be safely treatable (can be synchronous or metachronous to primary tumor diagnosis) with curative intent OR
   2. OPD with 1 to 5 lesions progressing on a background of widespread but stable metastatic disease OR
   3. Systemic therapy-induced OMD where there are 1 to 5 persistent lesions after systemic therapy, all safely treatable with SABR

7. Single spinal level from C1 to L5 to be treated for the purpose of the study (co-existing lesion(s) on non-consecutive spinal level(s) may receive RT at Investigator discretion, if deemed unlikely to interfere with study treatment and assessment of outcomes).

8. Stable spine assessed by Spinal Instability Neoplastic Score (SINS) (SINS 0-6, or SINS 7-12 and not for surgical intervention).

9. Bilsky Grade 0-1a (i.e. minimal (epidural impingement, without deformation of thecal sac) or no epidural disease) as confirmed by Radiation Oncologist

10. Able to lie flat in the treatment position for radiotherapy for up to 60 minutes

11. Females of childbearing potential must not be pregnant or lactating, and must be prepared to take adequate contraception methods during treatment. Males whose female partners are of childbearing potential must be prepared to take adequate contraception methods during treatment. Examples of effective contraception methods are a condom or a diaphragm with spermicidal jelly, or oral, injectable or implanted birth control

Exclusion criteria

1. Previous radiotherapy or surgery to the proposed SABR treatment site which is likely to interfere with treatment or assessment of outcomes (for radiotherapy, this includes prior thoracic radiotherapy to the lung or oesophagus which would result in overlap of fields if a T spine lesion will be treated)
2. Patients with symptomatic spinal cord compression or cauda equina syndrome, resulting in bony compression or epidural compression of the spinal cord or cauda equine, respectively
3. Patients with syndromes or conditions associated with increased radiosensitivity
4. Patients with radiosensitive histologies, e.g. myeloma or lymphoma
5. Contraindication to MRI, e.g. MRI-incompatible personal pacemaker in situ
6. Patients with pre-existing osteoporotic fractures of the spine
7. Prior treatment with any radionuclide within 30 days prior to registration
8. Patients who have received chemotherapy within 1 week prior to administration of protocol RT or who are expected/planned to receive chemotherapy during RT or within 1 week after completing protocol RT
9. Uncontrolled intercurrent illness that is likely to interfere with treatment or assessment of outcomes, or psychiatric illness/social situations that would limit compliance with study requirements
10. Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study, or if it is felt by the research / medical team that the patient may not be able to comply with the protocol and follow-up schedule due to psychological, familial, sociological or geographical conditions
11. Significant or progressive neurological deficit such that emergency surgery or radiation required

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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126 participants in 2 patient groups

Low baseline VCF risk

Experimental group

Description:

All of: * No VCF * Predominantly sclerotic lesion (as determined by the Investigator based on MRI) * Normal spinal alignment * \<50% vertebral body involvement

Treatment:

Radiation: Radiation: image guided dose escalated SABR using a simultaneous integrated boost (SIB)

High baseline VCF risk

Experimental group

Description:

Any of: * Pre-existing VCF * Predominantly lytic lesion (as determined by the Investigator based on MRI) * Spinal deformity * ≥50% vertebral body involvement

Treatment:

Radiation: Radiation: image guided dose escalated SABR using a simultaneous integrated boost (SIB)