This is a Pilot clinical trial determining the safety of an active surveillance approach to local therapy in subjects with brain metastases. These are subjects who are undergoing CNS-penetrating systemic therapy.
Study Type
OBSERVATIONAL
Enrollment
12
Chao Family Comprehensive Cancer Center, University of California, Irvine
Orange, California, United States
RECRUITINGFeasibility of Enrolling Patients
Feasibility of enrolling patients as measured by percentage of patients enrolled compared to the anticipated study accrual.
Time frame: 1 year
Feasibility of completing required surveillance imaging
Feasibility of completing required surveillance imaging as measured by percentage of enrolled patients that complete surveillance imaging.
Time frame: 1 year
Feasibility of administering Cognitive Assessments
Feasibility of completing required Cognitive Assessments as measured by percentage of enrolled patients that complete QOL and Cognitive Assessments..
Time frame: 1 year
Feasibility of administering QOL Questionnaires
Feasibility of completing required Quality of Life (QOL) Questionnaires as measured by percentage of enrolled patients that complete QOL and Cognitive Assessments..
Time frame: 1 year
Incidence of pre-defined safety events
Number of subjects who experience incidence of pre-defined safety events associated with progression of intracranial disease while on systemic therapy
Time frame: 1 year
Chao Family Comprehensive Cancer Center University of California, Irvine
CONTACT
University of California Irvine Medical
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.