LITT Followed by Hypofractionated RT for Recurrent Gliomas

Description

The purpose of this study is to evaluate the treatment regimen of using Laser Interstitial Thermal Therapy (LITT) and Hypo-fractionated Radiation Therapy to treat patients with recurrent gliomas.

Conditions

Glioblastoma, Brain Tumor, Glioma, Neoplasms

Study Overview

Study Details

Study overview

The purpose of this study is to evaluate the treatment regimen of using Laser Interstitial Thermal Therapy (LITT) and Hypo-fractionated Radiation Therapy to treat patients with recurrent gliomas.

Pilot Study of Laser Interstitial Thermal Therapy Followed By Hypofractionated Radiation Therapy for Treatment of Recurrent Gliomas.

LITT Followed by Hypofractionated RT for Recurrent Gliomas

Condition
Glioblastoma
Intervention / Treatment

-

Contacts and Locations

Baltimore

University of Maryland Greenebaum Cancer Center, Baltimore, Maryland, United States, 21201

Bel Air

UCH Kaufman Cancer Center, Bel Air, Maryland, United States, 21014

Columbia

Central Maryland Radiation Oncology, Columbia, Maryland, United States, 21044

Glen Burnie

Baltimore Washington Medical Center, Glen Burnie, Maryland, United States, 21061

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patients with history of a WHO Grade II-IV glioma with radiographic evidence of recurrent or progressive tumor
  • * Patient must have received prior radiation therapy for initial treatment of glioma
  • * Patients with any number of recurrences are allowed as long as the patient has not undergone re-irradiation
  • 2. Brain MRI with contrast demonstrates an enhancing tumor ≤ 6 cm in largest diameter within 60 days prior to registration
  • 3. History and physical including neurological exam within 30 days prior to registration
  • 4. Karnofsky performance status ≥ 60% within 30 days prior to registration
  • 5. Age ≥ 22 years old
  • 6. Minimum interval since completion of prior radiation treatment is 8 weeks
  • * Patients will only receive re-irradiation if pathology from LITT is consistent with recurrent tumor
  • 7. Patients must have signed an approved informed consent
  • 8. Patients with the potential for pregnancy or impregnating their partner must agree to practice effective contraceptive methods to avoid conception while on study and for 6 months after study completion.
  • 9. Female patients of child-bearing potential must have a negative pregnancy test within 28 days prior to study registration.
  • 1. Patients that are not surgical candidates for stereotactic biopsy or laser ablation
  • 2. Patients with impaired cardiac function or clinically significant cardiac diseases, including any of the following:
  • * History or presence of serious uncontrolled ventricular or significant arrhythmias.
  • * Any of the following within 6 months prior to registration: myocardial infarction, severe/unstable angina, coronary artery bypass graft, congestive heart failure, cerebrovascular accident, transient ischemic attack , pulmonary embolism
  • 3. Infratentorial tumor or evidence of leptomeningeal spread
  • 4. Inability to undergo a MRI
  • 5. Pregnant or breast-feeding women

Ages Eligible for Study

22 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Maryland, Baltimore,

Study Record Dates

2026-12