Stereotactic Radiotherapy for SPinal Metastases With Limited Extent of Epidural Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorInstitut Cancerologie de l'Ouest

About this trial

This study evaluates a new radiation treatment approach for patients with cancer that has spread to the spine (vertebral metastases) and involves limited extension around the spinal cord without causing compression (non-compressive epiduritis). This condition is common and can lead to serious complications, including pain and spinal cord compression, potentially affecting mobility and quality of life.

The current standard of care is conventional radiotherapy, which is effective for symptom relief but may provide limited long-term tumor control. As advances in cancer treatments have improved survival, there is an increasing need for treatment approaches that better prevent local tumor progression in the spine.

This randomized clinical trial compares standard radiotherapy with stereotactic radiotherapy (SRT), an advanced and highly precise radiation technique that delivers higher doses directly to the tumor while minimizing exposure to surrounding healthy tissues, including the spinal cord.

The primary objective is to determine whether SRT can improve local disease control while maintaining an acceptable safety profile. The study will evaluate the proportion of patients who are alive without spinal disease progression (including spinal cord compression or local tumor recurrence) at one year after treatment. Secondary outcomes include treatment-related side effects, time to disease progression, overall survival, quality of life, feasibility of delivering SRT within a defined timeframe, risk of vertebral fractures, and need for additional radiation treatment.

Eligible patients will have an estimated life expectancy greater than six months. Strict radiation dose constraints will be applied to minimize the risk of spinal cord injury, and patient safety will be closely monitored, including implementation of an early stopping rule in case of unexpected severe toxicity.

The hypothesis of the study is that stereotactic radiotherapy will improve local control of spinal metastases compared with standard radiotherapy, without increasing the risk of serious adverse effects.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Histologically confirmed solid tumor;

Vertebral bone metastasis located between C2 and S1 (inclusive) with epiduritis (spinal cord or cauda equina) without clinical and/or radiological spinal cord compression on MRI;

Performance status (PS) ≤ 1;

Spinal Instability Neoplastic Score (SINS) ≤12;

Disqualifiers

Neurological deficit attributable to spinal cord compression or cauda equina syndrome;

Patient experiencing pain that prevents lying down for 30 minutes despite optimal analgesic treatment;

Life expectancy ≤6 months as estimated by the investigator;

Neurosurgical indication (preventive or decompressive) prior to radiotherapy;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Stereotactic Body Radiotherapy (SBRT)

    Radiation

    Stereotactic body radiotherapy delivered in 5 fractions, consisting of 20 Gy to the involved vertebra and spinal canal (including adjacent hemi-vertebrae) with a simultaneous integrated boost to 35 Gy in 5 fractions to the tumor volume, according to protocol-defined delineation and dose constraints.

  • Conventional External Beam Radiotherapy

    Radiation

    Conventional external beam radiotherapy delivered in 5 fractions with a total dose of 20 Gy to the involved vertebra and spinal canal, including adjacent hemi-vertebrae, in accordance with standard palliative practice.

Treatment groups

167 Participants
are divided into 2 treatment groups
Group A: Stereotactic Body Radiotherapy (SBRT)Experimental treatment 1 intervention
Group B: Conventional Radiotherapy (palliative dose)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

1-year Clinical Disease Control Rate

Proportion of participants who are alive 12 months after randomization without clinical progression of the treated spinal lesion and without neurological deterioration attributable to the treated lesion during the 12-month follow-up.

Time frame
12 months after randomization

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: