This study is a prospective evaluation of systemic, intravenous high-dose methotrexate (HD-MTX, 8 g/m2) in patients with triple negative, HER2-positive, and hormone refractory breast cancer with leptomeningeal metastasis (LMD) with or without brain parenchymal involvement.
Primary Objective: \- To assess if treatment with systemic intravenous high-dose methotrexate (HD-MTX) will result in an overall survival (OS) exceeding 12 weeks at 80% among patients with triple negative, HER2-positive, and hormone refractory metastatic breast cancer patients with leptomeningeal metastasis (LMD) with and without parenchymal brain involvement. Secondary and Exploratory Objectives * To describe the one-year survival in patients with LMD from metastatic breast cancer treated with HD-MTX. * To describe the overall progression free survival (PFS) in patients with LMD from metastatic breast cancer treated with HD-MTX. * To describe the tolerability of HD-MTX in patients with LMD from metastatic breast cancer. * To describe the cost of HD-MTX treatment in patients with LMD from metastatic breast cancer. * To investigate cytologic sterilization following HD-MTX in patients with LMD from metastatic breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Enrolled patients will undergo treatment with HD-MTX (8 g/m2) as per current standard practice on an every 2 week schedule until disease progression or death from any cause. Treatment will be performed according to standard clinical practice. Surveillance imaging with or without cytologic evaluation will be performed as per standard clinical practice after every 2 cycles (\~28 days). Treatment will continue until there is unequivocal evidence of clinical or radiographic CNS or systemic disease progression, death from any cause, or intolerance.
Sidney Kimmel Comprehensive Cancer Center
Baltimore, Maryland, United States
RECRUITINGSiteman Cancer Center- Washington University School of Medicine in St. Louis
St Louis, Missouri, United States
ACTIVE_NOT_RECRUITINGComprehensive Cancer Center at Wake Forest University (CCCWFU)
Winston-Salem, North Carolina, United States
RECRUITINGOverall Survival (at 12 weeks)
The primary endpoint is survival at 12 weeks from first date of treatment. For the primary analysis, this will be dichotomized according to whether the patient achieves an OS greater than 12 weeks (i.e. survival rate). This cutoff has been selected based on reported OS data in historical controls.
Time frame: 12 weeks
One year survival
As defined as the proportion of patients with time to death greater than 12 months from the time of first date of treatment.
Time frame: 1 year
Progression Free Survival
Progression free survival as defined as the time from first date of treatment to the time of systemic or neurologic progression of disease whichever occurs first. Neurologic progression will be defined as the minimum of clinical or radiographic progression. Clinical neurologic progression will be defined by neurologic examination demonstrating objective, new neurologic deficit attributable to the underlying LMD. Radiographic progression (neurologic or systemic) will be defined by RECIST criteria.
Time frame: From date of first treatment to the time of systemic or neurologic progression of disease whichever occurs first, assessed up to 2 years
Tolerability of Treatment - Number of Grade 3 or Higher Adverse Events
Toxicity as grade 3 and higher will be tabulated by reporting period, where reporting period is defined to be the planned 14 day period between administrations of high-dose methotrexate (HD MTX).
Time frame: Up to 2 years
Number of Treatment Delays
Toxicities related to dose delays will be recorded by reporting period, where reporting period is defined to be the planned 14 day period between administrations of HD MTX. The number of times treatment is delayed divided by the number of reporting periods administered to all patients on study will be used to characterize the fraction of times treatments must be delayed.
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Time frame: Up to 2 years
Number of Dose Reductions
Toxicities related to dose delays will be recorded by reporting period, where reporting period is defined to be the planned 14 day period between administrations of HD MTX. The number of times treatment is delayed divided by the number of reporting periods administered to all patients on study will be used to characterize the fraction of times treatments must be delayed.
Time frame: Up to 2 years