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NCT Number: NCT05124236

Trial of Preoperative Radiosurgery Versus Postoperative Stereotactic Radiotherapy for Resectable Brain Metastases

The research question is whether a single fraction of preoperative radiosurgery can reduce the incidence of leptomeningeal disease 12 months following resection of a brain metastasis (BM) as compared with 5 fractions of postoperative stereotactic radiotherapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tirol Kliniken Innsbruck, Innsbruck, Austria

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About this study

Neurosurgical resection of a brain metastasis in patients with a diagnosis of cancer may be indicated however the recurrence rate approximates 50% and adjuvant radiotherapy is standard. Single fraction postoperative stereotactic radiosurgery (SRS) has been widely adopted as a standard therapy as it achieves equivalent survival and prevents loss of neurocognitive function as compared with whole brain radiotherapy and improves cavity local control rates as compared with observation. Hypofractionated stereotactic radiotherapy in 3 to 5 fractions (hfSRT) is also used in the postoperative setting.

Nodular leptomeningeal disease (nLMD) is a recognised pattern of failure after postoperative SRS and hfSRT. A 16.9% incidence of nodular LMD was seen after surgery and a similar incidence of 11%-28%is reported following postoperative SRS in retrospective series. These data suggest that postoperative SRS/hfSRT have no significant effect on the development of LMD following surgery.

The incidence of LMD following single fraction preoperative SRS is only 6.1% according to the largest retrospective series. Preoperative SRS takes advantage of the easier delineation of an intact BM and sterilizes tumor cells disseminated at surgery. Side effects are minimized by a smaller planning margin, a dose reduction and resection of the irradiated volume. In addition, there is no delay to systemic therapy due to wound healing/complications. Furthermore, a single fraction offers patient convenience.

This trial will randomise and compare intracranial outcomes between single fraction preoperative SRS and 5 fraction postoperative hFSRT.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Age ≥18
  • Karnofsky performance status ≥60
  • Histological diagnosis of a malignant primary or metastatic tumour
  • Ability to take steroids
  • No contraindication to magnetic resonance imaging (MRI)
  • MRI-diagnosis of a clearly demarcated contrast-enhancing brain metastasis up to 4.0 cm diameter indicated for neurosurgical resection (tumorboard decision). Up to 3 other brain metastases suitable for primary radiosurgery/ stereotactic radiotherapy
  • Survival estimated by primary clinician > 12 months
  • Platelet count > 100/ml, INR < 1.3, Hb > 7.5 g/dL

Exclusion criteria

  • Radiosensitive histology: germ cell tumour, lymphoma, multiple myeloma
  • >10 mm midline shift, effacement of the 4th ventricle or other sign of raised intracranial pressure requiring urgent decompressive surgery
  • More than 4 brain metastases or the diameter of the metastasis for resection >4.0 cm.
  • More than 1 metastasis requiring resection
  • Leptomeningeal disease in the CSF or on MRI (unless localized and can be irradiated then resected with the metastasis)
  • Prior radiation to the brain (SRS/SRT to lesion to be resected and /or WBRT)
  • Prior resection of a primary or secondary brain tumor
  • Prior diagnosis of a non-meningioma brain tumor
  • Prior radionuclide therapy within 30 days
  • Prior anti-VEGF therapy within 6 weeks
  • Unable to tolerate radiosurgery immobilization and treatment
  • Inability to give informed consent
  • Pregnancy or lactation
  • Females of reproductive potential not willing to use effective contraception for at least 6 months after radiotherapy
  • Males of reproductive potential not effective contraception for 3 months after radiotherapy
  • Lack of likely compliance with protocol and follow-up

Treatment and study plan

preoperative radiosurgery

Radiation

single fraction radiosurgery

postoperative hypofractionated stereotactic radiotherapy

Radiation

fractionated stereotactic radiotherapy /radiosurgery in 1 to 6 fractions according to local standard of care

Primary outcomes

  1. Leptomeningeal disease

    Time frame: 12 months after intervention

    time to leptomeningeal disease

Secondary outcomes

  1. Local control of the surgical cavity

    Time frame: 12 months after intervention

    No evidence of tumour recurrence on contrast-enhanced MRI

  2. Distant brain failure

    Time frame: 12 months after intervention

    New brain metastases

  3. Radionecrosis

    Time frame: 12 months after intervention

    Adverse radiation effects

  4. Quality of life assessment

    Time frame: 3,6,12 months after intervention

    EORTC questionnaire core questionnaire QLQ30, EORTC questionnaire brain module BN 20 (1-4, low scores reflect better QoL)

Study contacts

Contact information is provided by the study sponsor or research team.

Oliver Riesterer, Prof.

CONTACT

[email protected]

+41 62 838 4249

Susanne Rogers, MD PhD

CONTACT

[email protected]

+41 62 838 57 26

Sponsors and collaborators

Lead sponsor

Susanne Rogers

Other

Collaborators

  • University of Basel

Registry information

Official study title

A Multicenter Prospective, Interventional, Randomized Trial of Preoperative Radiosurgery Compared With Postoperative Stereotactic Radiotherapy for Resectable Brain Metastases

Acronym: PREOP-2

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Nov 17, 2021
Registry last updated
Mar 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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