An Investigational Scan (hpMRI) for Monitoring Treatment Response in Patients With Thyroid Cancer and Other Malignancies of the Head and Neck Undergoing Radiation Therapy and/or Systemic Therapy

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

This trial investigates whether hyperpolarized magnetic resonance imaging (hpMRI) can predict treatment response in patients with thyroid cancer and other malignancies of the head and neck undergoing radiation therapy and/or receiving systemic therapy before surgery. An hpMRI is like a standard MRI but involves the use of an imaging contrast agent called hyperpolarized 13-C-pyruvate. Diagnostic procedures, such as hpMRI, may predict a patient's response to treatment and may help plan the best treatment.

Eligibility criteria

Qualifiers

Be willing and able to provide informed consent

Be informed of the investigational nature of this study

Be diagnosed with thyroid cancer and other malignancies of the head and neck with intent for treatment

Disqualifiers

Have a history of severe claustrophobia

Have electrically, magnetically or mechanically activated implants that would preclude magnetic resonance imaging (MRI)

Have a history of cardiac arrhythmia

Have an allergy to Gadavist intravenous contrast

Trial design

Treatments tested in this trial

  • Hyperpolarized Carbon C 13 Pyruvate
  • Magnetic Resonance Imaging
  • Magnetic Resonance Imaging

Treatment groups

42 Participants
are divided into 2 treatment groups

Sponsors and collaborators

M.D. Anderson Cancer Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator