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Completed

NCT Number: NCT02654106

Stereotactic Radiotherapy Plus Temozolomide for Refractory Brain Metastases

This clinical trial was designed to investigate the efficiency and toxicity of fractionated stereotactic radiotherapy(FSRT) combined with Temozolomide(TMZ) for refractory brain metastases.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, 100021, China

About this study

This is a single-arm, single center, phase II trial to investigate the feasibility and toxicity of FSRT plus TMZ for refractory brain metastases, which are defined as A: multiple brain metastases(≥3 lesions); B: large brain metastases(with one lesion's volume is no smaller than 6cc or the longest diameter is no shorter than 3cm); C: meningeal metastases.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologic or cytologic diagnosis of primary tumor and conformed brain metastases by enhanced MRI or CT
  • the lesion number is no less than 3; or the tumor volume is no smaller than 6cc; or tumor diameter is no shorter than 3cm; or uncontrolled brain tumor after whole brain radiotherapy(WBRT); or the tumor is adjacent to essential structures of the brain, such as brain stem, optic chiasma, optic tract, etc.
  • KPS ≥60,or KPS ≥40 and the limitation of motion is simply caused by brain tumor that is adjacent to the motor function areas.
  • Age: 18-75 years old.
  • Adequate end-organ function:

WBC≥4.0x109/L Neu ≥ 1.5x109/L Hemoglobin ≥ 110 g/L Platelets ≥100 x109/L Total bilirubin ≤ 1.5x ULN AST and ALT ≤ 1.5x ULN BUN and Cr: within the normal range

Exclusion criteria

  • Other clinically significant diseases (e.g.myocardial infarction within the past 6 months, severe arrhythmia).
  • Unable or unwilling to comply with the study protocol.
  • The expected survival time is less than 3 months.
  • Patients who are anticipated in other clinical trials of brain metastases.
  • Patients who has been treated with SRT in other hospitals
  • Pregnant patients or female patients whose HCG is positive
  • Unsuitable to participate in study, that in the opinion of the treating physician.

Treatment and study plan

Fractionated Stereotactic Radiotherapy

Radiation

The regular fraction modes were as follows: a. lesions≥3 cm:52Gy/4Gy/13f or 52.5Gy/3.5Gy/15f; b. lesions<2cm:36Gy/12Gy/3f or 24Gy/24Gy/1f; for lesions located in function areas, it would be adjusted to 40Gy/8Gy/5f; c. lesions 2-3cm:40-48Gy/8-10Gy/6-4f; d. lesions located in brainstem:50-60Gy/2.5-3Gy/20f.

Other names: FSRT

Temozolomide

Drug

concomitant TMZ: 75mg/m2 adjuvant TMZ: 150mg/m2*5d, q28d, 6cycles

Other names: TMZ

Primary outcomes

  1. intracranial progress free survival rate

    Time frame: up to 2 years

    defined as no progress of the treated lesions and no distant progress in the brain

Secondary outcomes

  1. Overall survival rate

    Time frame: up to 3 year

  2. progress free survival rate

    Time frame: up to 1 year

  3. local control rate

    Time frame: up to 1 year

  4. disease control rate (DCR)

    Time frame: 2-3 months after radiation

    Using RTOG9508 criteria, Tumor control is defined as CR+PR+SD

  5. adverse event

    Time frame: from the day of radiation to the end of adjuvant TMZ,up to 6 months

    assessed by CTCAE criteria, v4.0 and RTOG criteria of the central nervous system

  6. causes of death

    Time frame: from the day of radiation to death date, up to 5 years

    collect the data of causes of death and analyze

Sponsors and collaborators

Lead sponsor

Chinese Academy of Medical Sciences

Other

Collaborators

  • Cancer Foundation, China

Registry information

Official study title

Fractionated Stereotactic Radiotherapy Combined With Temozolomide for Refractory Brain Metastases: A Single-arm, Single-center Phase II Trial

Acronym: SRTRBM

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Jan 13, 2016
Registry last updated
Jun 6, 2017

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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