Prospective Evaluation Of High-Dose Systemic Methotrexate In Patients With Breast Cancer And Leptomeningeal Metastasis

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorWake Forest University Health Sciences

About this trial

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.

Eligibility criteria

Qualifiers

Adults (male and female) age >18

Eastern Cooperative Group (ECOG) Performance Scale 0-1 (see Appendix I)

TRIPLE NEGATIVE (ER-negative, PR-negative, and HER2-negative disease). Triple-negative patients will be defined per ASCO-CAP Guidelines.

HER2-POSITIVE: HER2-positive patients will be defined per ASCO-CAP Guidelines.

Disqualifiers

Prior allergy or adverse reaction to methotrexate

New York Heart Association Heart Failure Class >3

Active diabetes insipidus

Active mucositis

Trial design

Treatments tested in this trial

  • High-dose Methotrexate (8 gm/m2; HD-MTX)

Treatment groups

16 Participants
are divided into 1 treatment group

Locations

3
Sidney Kimmel Comprehensive Cancer Center21287, BaltimoreMaryland, United States
Siteman Cancer Center- Washington University School of Medicine in St. Louis63130, St LouisMissouri, United States
Comprehensive Cancer Center at Wake Forest University (CCCWFU)27157, Winston-SalemNorth Carolina, United States

Sponsors and collaborators

Wake Forest University Health Sciences

Lead sponsor

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Collaborator

National Cancer Institute (NCI)

Collaborator