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Intraoperative Radiotherapy After the Resection of Brain Metastases

NCT03226483 — Not applicable, Unknown, 50 participants, Universitätsmedizin Mannheim

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Intraoperative Radiotherapy After the Resection of Brain Metastases - a Phase II Feasibility Study

RegistryNCT03226483, acronym INTRAMET
StatusUnknown
PhaseNot applicable
Study typeInterventional; na, single group, masking: none, treatment
Enrollment50 (Estimated)
SponsorUniversitätsmedizin Mannheim (Other)
ConditionsBrain Metastases
InterventionsIntraoperative Radiotherapy (Radiation)
Datesstart 2017-03-28, primary completion 2023-12-31 (estimated), completion 2023-12-31 (estimated), first posted 2017-07-21, last updated 2022-06-03
Locations1 site in Germany

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-Summary

INTRAMET examines prospectively the effectiveness of an intraoperative radiotherapy immediate after the surgical resection of brain metastases. Patients won't receive further radiation therapy of the intraoperatively treated lesion.

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+Detailed description

Brain metastases occur in up to 40% of all patients diagnosed with systemic cancer. Without adjuvant radiotherapy after resection of space occupying lesions local recurrence rates are high. That is why guidelines recommend a cavity boosting with x-rays. External beam radiotherapy can lower the risk of local recurrence but means longer hospitalization, prolongs the time to systemic salvage therapies and bears risks of radionecrosis and leucoencephalopathy with neurological and cognitive decline. A solution for this problem could be onetime intraoperative radiotherapy (IORT) with soft x-rays to sterilize the resection cavity, which may provide both: freedom from local recurrence fast track salvage therapy initiation.

INTRAMET is a single institution, open-label, prospective, phase 2 feasibility study for intraoperative radiotherapy immediately following resection of brain metastases. 50 adult patients with resectable not dural brain metastases should be treated in surgery after tumor resection with IORT with 20-30Gy prescribed to the margin of the resection cavity. The highest dose tolerable to surrounding risk structures (N. opticus, brainstem) should be used.

With this method, the investigators hope to show similar local control rates to postoperative external beam radiotherapy in line with guideline recommendations with less patient hospitalization and faster start of rescue therapies which could lead to a favorable overall outcome and less cognitive side effects.

+Arms and interventions

ArmTypeInterventionsDescription
Intraoperative radiotherapyExperimentalRadiation: Intraoperative RadiotherapyAfter neurosurgical resection and proven metastasis (frozen section) a local intraoperative radiotherapy with soft energy x-rays is applied to the resection cavity. To perform this an applicator is inserted into the situs in the tightest fit rule. The highest possible dose between 30-20 Gy is chosen depending on nearby risk structures (Optic nerve, brainstem) is prescribed. After radiotherapy the applicator is removed and the surgery will be finished in standard way.
  • Intraoperative Radiotherapy (Radiation): Intraoperative Radiotherapy is performed with a mobile radiation device emitting soft energy x-rays in a spherical way. Different size applicators are available to cover the resection cavity after the tightest fit rule.

+Outcome measures

Primary outcomes

  • Median local progression-free-survival [2 years]: Rate of recurrence of the treated lesion in the brain

Secondary outcomes

  • Overall-survival [5 years]: Survival differentiated between death due to systemic cancer progress and death due to cerebral progress
  • Time to further therapy [6 month]: Time to further cancer therapy (e.g. salvage chemotherapy)
  • Patients cognitive performance [5 years]: Neuropsychological battery
  • Patients quality of life [5 years]: Patient questionary
  • Global progression-free-survival [2 years]: Systemic cancer progression-free-survival
  • Regional progression-free-survival [2 years]: Progression-free survival concerning other brain metastases
  • Intraoperative radiotherapy caused dose-limiting toxicities [6 month after intervention]: Occurrence of wound healing disorders or infection requiring surgical revision, cerebral bleeding or ischemia, radionecrosis requiring surgical intervention

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Karnofsky Performance index ≥ 50%
* MRI T1 Gadolinium enhancing non-dural resectable lesion
* Informed consent
* Adequate birth control
* Frozen section confirms metastasis
* Adequate distance to optic nerve and brainstem

Exclusion Criteria:

* Dural lesions or meningeal carcinomatosis
* Frozen section reveals glioma, lymphoma,small cell lung cancer or germinoma
* Psychiatric or social condition interfering compliance
* Contraindication against anesthesia, surgery, MRI and/or Gadolinium
* Pregnant or breast-feeding women

+Locations (1)

FacilityCityCountryStatus
Universitätsmedizin MannheimMannheimGermanyRecruiting

+Investigators

My Notes