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NCT Number: NCT05346367

Improving Therapeutic Ratio With Hypo Fractionated Stereotactic Radiotherapy for Brain Metastases

Randomized phase II trial. The study aims to investigate a different and potentially safer radio therapeutic treatment method for brain metastases. The current standard of stereotactic radiotherapy (SRT) in one or three fractions is compared to fractionated stereotactic radiotherapy (fSRT) in five fractions.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Haaglanden Medisch Centrum

Leidschendam, South Holland, 2262 BA, Netherlands

Location status: Recruiting

Location contact

Jaap Zindler, Dr

CONTACT

[email protected]

Ursula Fisscher, PhD

CONTACT

[email protected]

About this study

Randomized phase II trial. Stereotactic radiotherapy is one of the most frequently chosen treatment options for brain metastases. There are an increasing number of long term survivors. Brain necrosis (e.g. radio necrosis) is the most important long term side effect of the treatment, occurring in up to 40% of patients, dependent on the size of the metastasis and delivered radiotherapy dose. Retrospective studies have shown that the incidence of radio necrosis, as well as local tumor recurrence, can be decreased with a risk difference of around 20% by administrating fractionated stereotactic radiotherapy (fSRT, e.g. five fractions) over single fraction stereotactic radiotherapy, especially in large brain metastases. In this trial, one group is treated with SRT in one or three fractions. The other group is treated with fSRT in five fractions. Survival, toxicity and patient reported quality of life are monitored.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • At least one brain metastasis of large cell cancer suitable for SRT
  • Karnofsky Performance Status ≥ 70
  • Ability to provide written informed consent
  • New brain metastases during follow-up after surgery allowed (when outside of resection cavity area)
  • New brain metastases during follow-up after previous SRT allowed (when outside of previous irradiation field)

Exclusion criteria

  • Contra-indication for MRI scan
  • Primary tumor of small cell lung cancer, germinoma or lymphoma
  • Prior whole brain radiotherapy or SRT on the current target brain metastases (in field re-irradiation)
  • Presence of leptomeningeal metastases
  • Previous inclusion in the SAFESTEREO study

Treatment and study plan

SRT

Radiation

SRT

FSRT

Radiation

fSRT

Primary outcomes

  1. radio necrosis or local failure

    Time frame: 2 years after treatment

    Incidence of either radio necrosis or local failure according to Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM).

Secondary outcomes

  1. Survival

    Time frame: 2 years after treatment

    median survival with Kaplan Meyer analysis

  2. symptomatic radio necrosis (RN) or local failure (LF)

    Time frame: 2 years after treatment

    incidence of RN or LF within 2 years after SRT

  3. salvage treatment

    Time frame: 2 years after treatment

    incidence of salvage treatment within 2 years after SRT

  4. distant brain recurrences

    Time frame: 2 years after treatment

    incidence of distant brain recurrences within 2 years after SRT

  5. Dose dexamethasone

    Time frame: baseline - 2 years after treatment

    Dose dexamethasone in mg per day

  6. Anti-epileptic drug use

    Time frame: baseline - 2 years after treatment

    Anti-epileptic drug use in mg per day

  7. Grade 2 or more toxicity (CTCAE v5.0)

    Time frame: baseline - 2 years after treatment

    incidence of Grade 2 or more toxicity according to CTCAE version 5.0 within 2 years after SRT

Study contacts

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

Jaap D Zindler, MD, PhD

CONTACT

[email protected]

+31-88-9792013

Mirjam Mast, PhD

CONTACT

[email protected]

+31-88-9792013

Sponsors and collaborators

Lead sponsor

Haaglanden Medical Centre

Other

Registry information

Acronym: SAFESTEREO

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Apr 26, 2022
Registry last updated
Mar 12, 2024

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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