Intraoperative Radiotherapy in Patients With Brain Metastases

Parc de Salut Mar

Status: Enrolling

Conditions: Brain Metastases

Treatments: Radiation: Intraoperative radiotherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT04847284

2020/9548/I

Details and patient eligibility

About

Intraoperative radiotherapy (IORT) is a new alternative for local radiotherapy with the advantages of dose escalation, reduced overall treatment time, and enhanced patient convenience, however the degree of efficacy is unknown, as well as and which is the most efficient dose.

The objective of this study is to evaluate the efficacy and safety of IORT in patients with surgical excision of brain metastases at a dose of 20 Gy is at least as effective and safe as other forms of radiation therapy in patients with resection of brain metastases.

Full description

1. INTRODUCTION

   Brain metastases occur in roughly 30% of all cancer patients during their course of disease. Their incidence is believed to rise due to the aging population that develops more cancer per se, an increase in overall survival due to more effective extracranial therapies but with only few (novel) substances crossing the blood-brain barrier and more broadly available and more advanced imaging techniques.

   Neurosurgical treatment remains a cornerstone in the management of brain metastasis, especially for lesions causing mass effects or neurological deficits or in case tissue is necessary to establish a diagnosis. As local recurrence rates are as high as 50-60% after surgical resection alone, adjuvant therapies to prevent such are necessary.

   Whole brain radiotherapy (WBRT) does not influence survival but rather impairs neurocognitive functions and, as histologic in-depth exams of cavity borders showed that most brain metastases infiltrate only 0.3-1.2 mm into the surrounding healthy brain tissue, therefore treatment is to date usually confined to the cavity margin. Thus, the currently recommended standard of care is post-operative stereotactic radiosurgery (SRS) to the resection cavity. One of the drawbacks of this modality is the incidence of radionecrosis, especially in large tumor volumes. As an alternative to radiosurgery, hypofractionated local radiotherapy is also used, reducing the risk of radionecrosis in large volumes. There are no prospective randomized studies comparing both techniques.

   The need to find a modality of radiotherapy that achieves al least the efficacy of radiosurgery or hypofractionated local radiotherapy, without the disadvantages thereof, makes IORT as a possible treatment alternative.

   The objective of this study is to evaluate the efficacy and safety of IORT in patients with surgical excision of brain metastases at a dose of 20 Gy is at least as effective and safe as other forms of radiation therapy in patients with resection of brain metastases.

2. OBJECTIVES

   Primary Objective

   • Median local progression free survival (lPFS), defined as time span (in months) between surgery and recurrence within a 0,5 cm margin around the resection cavity, assessed by serial MRI scans and RANO response assessment criteria for brain metastases .
   • Radiation-related (acute / late) neurotoxicity, assessed by regular neurological examinations and serial MRI scans.

   Secondary objectives

   • Median regional PFS (rPFS), resembling the time (in months) from surgery to any progression outside of the 0,5 cm margin around the resection cavity, assessed by serial MRI scans and RANO response assessment criteria for brain metastases .
   • Global PFS (gPFS), defined as the time (in months) from surgery to any intra- and extracranial tumor progress.
   • Median overall survival (OS), defined as the time (in months) from surgery of brain metastases to death from by any cause.

3. DESIGN

This trial is an open, single arm, single institution, prospective trial to determine the efficiency and safety of IORT with low-energy photons to the cavity after resection of brain metastases. A total of 25 patients will be included.

Enrollment: 25 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥ 18 years
• Karnofsky Performance Status ≥ 70
• Newly diagnosed cerebral or cerebellar lesion (contrast enhancing on a T1-weighted MRI scan) amenable to total resection with no dural attachment
• Frozen section confirming a metastasis of an extracranial ( Central Nervous System i.e. non-CNS) tumor
• Adequate distance to optic nerve(s), chiasm and brainstem (organs at risk for radiotherapy)
• Adequate birth control

Exclusion criteria

• Leptomeningeal spread and dural attachment (assessed pre- and intraoperatively)
• Frozen section reveals primary CNS tumor, lymphoma, SCLC (Small-cell lung cancer) or germinoma
• More than one brain metastasis
• Psychiatric or social condition potentially interfering with compliance
• Contraindication against anesthesia, surgery, MRI and/or contrast agents
• Pregnant or breast-feeding women

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

Single arms

Experimental group

Description:

To determine the efficiency and safety of IORT with low-energy photons to the cavity after resection of brain metastases

Treatment:

Radiation: Intraoperative radiotherapy