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Serial Magnetic Resonance Imaging for the Prediction of Radiation-Induced Changes in Normal Tissue of Patients With Oral Cavity or Skull Base Tumors

RecruitingPhase 4

Serial Magnetic Resonance Imaging of Longitudinal Radiotherapy-Attributable Normal Tissue Injury

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

All Cohorts:

* Patients older than 18 years of age
* Patients with good performance status (ECOG score 0-2)
* Patients willing to give written informed consent.

Cohort 1 (Individuals without ORN or MRONJ):

* Patients with histologically proven malignant neoplasms of the oral cavity, oropharynx or skull base.
* Patients currently dispositioned to treatment with radiotherapy and/or antiresorptive or antiangiogenic medication therapy

Cohort 2 (Individuals with ORN or MRONJ):

* Patients with a clinical diagnosis of ORN or MRONJ following treatment for cancer
* Patients previously dispositioned to treatment with radiotherapy and/or antiresorptive or antiangiogenic medication therapy

Exclusion Criteria:

* Patients unable to tolerate DW-MRI or DCE-MRI or having an estimated GFR \< 30ml/min/1.73m2.
* Patients with contraindication to MRI (e.g. non-MRI compatible metallic implants)

About the study

This phase IV trial studies how well serial magnetic resonance imaging (MRI) after radiation therapy works in predicting radiation-induced changes in the normal tissue of patients with oral cavity or skull base tumors. Performing MRIs after radiation therapy for patients with oral cavity or skull base tumors may help to predict osteoradionecrosis (a change in non-cancerous tissue).

What is being tested

Sponsor: M.D. Anderson Cancer Center · Participants: 425 · Started: Sep 17, 2018

Contact the study team

Official record on ClinicalTrials.gov — NCT04265430

Locations in the U.S.

TexasM D Anderson Cancer Center, Houston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.