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OpenTrials
Completed

NCT Number: NCT00916877

Prophylactic Cranial Irradiation in Patients With HER-2-Positive Metastatic Breast Cancer

Though brain metastases are a risk in all patients with breast cancer, those with HER-2 overexpression are at significantly greater risk. One series estimated a 30% incidence of brain metastases in this population, while another study found an incidence of approximately 40%. Traditional systemic therapies do not cross the blood brain barrier to any significant degree or at all, but radiation treatment can be effective in the treatment of intracranial metastases.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Cross Cancer Institute

Edmonton, Alberta, T6G 1Z2, Canada

About this study

The rationale for PCI is that the brain is a sanctuary site where cancer cells can remain inaccessible to chemotheraphy and agents such as trastuzumab due to the blood brain barrier, which prevents potentially harmful chemicals such as chemotherapy agents and antibodies such as trastuzumab from reaching the brain. Decreasing the incidence of brain metastasis with acceptable effects on neurocognitive function would be a significant improvement in the care of patients with MBC.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Female with HER2-positive disease
  • 18 years of age or older
  • ECOG greater or equal to 2
  • Life expectancy greater or equal to 6 months
  • Able to complete self administered quality of life evaluations and neurocognitive testing
  • Willing and able to comply with study instructions and commit to all clinic visits for the duration of the study
  • Women of child-bearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test at the baseline visit and must use highly effective birth control during study
  • Signed informed consent form

Exclusion criteria

  • Current malignancy in the brain, as determined by screening MRI/CT done no more then 6 weeks prior to study treatment with PCI
  • Chemo or radiation planned during the period when patients will receive study treatment with PCI
  • Prior radiotherapy of the brain
  • Prior stroke or brain hemorrhage in the 6 months prior to screening
  • History of neurological/psychiatric disorders, including psychotic disorders or demential, or any other reason, which may affect neurocognitive assessment
  • Inadequate renal function
  • Other known previous or concomitant serious illness or medical condition that may interfere with participation in the study

Treatment and study plan

Prophylactic Cranial Irradiation

Radiation

Prophylactic Cranial Irradiation

Primary outcomes

  1. To evaluate the safety of PCI, specifically with respect to neurocognitive function in patients with HER-2-positive metastatic breast cancer.

    Time frame: approximately 2 to 3 years from study start

Secondary outcomes

  1. To assess the impact of PCI on measures of survival, specifically brain metastases-free survival, overall progression free survival and overall survival

    Time frame: approximately 4 years from study start

Sponsors and collaborators

Lead sponsor

Alberta Health services

Other

Registry information

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Jun 10, 2009
Registry last updated
Aug 8, 2011

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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