Phase II Study of Intraventricular Methotrexate in Children With Recurrent or Progressive Malignant Brain Tumors

Nicklaus Children's Hospital f/k/a Miami Children's Hospital

Status and phase

Terminated

Phase 2

Conditions

Embryonal Tumor With Abundant Neuropil and True Rosettes

Recurrent Childhood Medulloblastoma

Childhood Atypical Teratoid/Rhabdoid Tumor

Metastatic Malignant Neoplasm to the Leptomeninges

Recurrent Childhood Ependymoma

Treatments

Drug: cyclophosphamide

Drug: topotecan

Drug: Intra thecal methotrexate

Study type

Interventional

Funder types

Other

Identifiers

NCT02684071

NCH-CNS-1601

Details and patient eligibility

About

Full description

The purpose of this research study is to test an experimental treatment method for recurrent or progressive brain tumors in children aged from 0-22 years. The use of methotrexate and chemotherapy (topotecan and cyclophosphamide) is experimental in this study. This means that their use by themselves or together has not been approved by the U.S. Food and Drug Administration for this usage. This study will attempt to determine via serial MRI scans if methotrexate administration into the lateral or fourth ventricle in combination with systemic intravenous topotecan and cyclophosphamide is effective in reducing tumor burden in the brain and spine for patients with recurrent or progressive brain tumors, including medulloblastoma, ependymoma, PNET (Primitive Neuroectodermal Tumor), atypical teratoid/rhabdoid tumor (AT/RT), and other malignant embryonal tumors. In addition, the study will evaluate the toxicity of the above mentioned experimental treatment during a two-year progression-free survival and survival of children with recurrent malignant brain tumors.

Enrollment

3 patients

Sex

All

Ages

Under 22 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Recurrent or progressive supratentorial or posterior fossa tumors with measurable disease on imaging studies of the brain and spine or CSF cytology.
Tumor histology, including: Medulloblastoma , PNET, or other embryonal tumor, Atypical teratoid/rhaboid tumor (AT/RT), and Ependymoma.
Leptomeningeal dissemination of a previously diagnosed CNS tumor.
Diagnosis of tumor pathology will be based upon pathology diagnosis from previous surgeries for patients with recurrent tumors.
Patients must have received prior radiation before current recurrence, unless the patient is less than 36 months old at diagnosis and has progressed after at least one upfront chemotherapy regimen in which case no prior radiation is required.
Patients must have a life expectancy of at least 12 weeks as indicated by the patient's oncologist and/or neurosurgeon.
Lansky or Karnofsky Performance status of at least 50.
Negative pregnancy test.
Specific organ function requirements for: Central Nervous System, Bone Marrow, renal and liver.

Exclusion criteria

Patients that do not meet the inclusion criteria above.
Pregnant or lactating female patients.
Patients currently enrolled in another experimental treatment protocol.
Patients with documented allergies to any of the chemotherapy agents used in this study.
Patient/Parent refuses study participation.
Patient is severely somnolent or comatose.
Unable or unwilling to commit to return or to follow-up visits.