Pre-Operative Nodal Staging of Thyroid Cancer Using Ultra-Small Superparamagnetic Iron Oxide Magnetic Resonance Imaging (USPIO MRI): Preliminary Study

In this research study each participant will have the study MRI (USPIO MRI) before he/she
undergoes surgery. Radiologists (doctors trained to read and understand this test) will
review this study MRI. The imaging results will be compared with the pathology reports from
the tissue removed during your surgery.

Before the research starts (screening):

After signing this consent form, the participant will be asked to undergo some screening
tests or procedures to find out if the participant can be in the research study. These
tests and procedures were done as part of regular care and would have been done even if it
turns out that the participant does not take part in the research study.

- An tumor assessment by CT (Computerized Tomography) scan or thyroid US
(ultrasonography) scans.

- If these tests show that the participant is eligible to participate in the research
study, they will begin the study. If the participant does not meet the eligibility
criteria, they will not be able to participate in this research study.

- Because women who are pregnant or nursing a baby cannot be in this research study, the
participant will have a urine pregnancy test if they are a woman of child bearing
potential. The participant cannot be in this research study if they are pregnant or
breastfeeding.

- The investigator will also ask if the participant is allergic to iron. Because the
study agent contains iron, the participant cannot be in this research study if they
have this allergy.

After the screening procedures confirm that the Participant is eligible to participate in
the research study:

The participant will have one research MRI scan:

On the first day, the participant will receive the contrast agent intravenously. This visit
will take about 30 minutes.

Before injecting the contrast medium, the investigator will clean the skin on the
participant's forearm with alcohol. Then the investigator will insert a small plastic tube
(IV) into a vein in the participant's forearm. The investigator will give the participant
the study agent, ferumoxytol, through the IV line. The dose of ferumoxytol and the rate of
administration will not be more than the dose the FDA has approved when people who have
anemia use this for iron replacement therapy. Before, during and until 30 minutes after the
participant get the ferumoxytol, the investigator will monitor (watch) the participant
closely for any reactions to the infusion. The participant will return to Massachusetts
General Hospital, Boston MA 02114, 48-72 hours for the post contrast MRI. The participant
will not receive Ferumoxytol before this MRI. This study visit will take about 45 minutes.

The participant will lie on a padded table. The table will move into a scanning machine. The
space in the scanning machine is very narrow, just a bit wider than that participant's body.
The participant will need to lie quietly for about 30 minutes while the images are being
taken. If the participant has problems with claustrophobia (fear or discomfort in small or
confined spaces), let the study doctor or a member of the staff know before enrolling in
this study.

During the MRI procedure, the participant will hear loud "banging" noises. This is the sound
the powerful magnets make during the test. The participant will be given earplugs to help
reduce the noise. The participant will also be able to talk to the MRI technologist during
the test and the technologist will be able to talk to the participant. If, during the test,
the participant feels too uncomfortable to continue, let the technologist know, and the test
will be stopped immediately.

If any of the participant's MRIs show unusual results that might be important for your
health, the study doctor will contact the participant's primary surgeon. The participant's
MRIs will be reviewed by a radiologist. They will be read and interpreted and the results
will be communicated to the participant's surgeon before scheduled surgery. The MRI scan
may show abnormal signals in lymph nodes that are outside the area that the surgeon normally
removes and the surgeon may decide to extend the surgery to include this additional area.
During the scheduled surgery, the participant's surgeon will remove the participant's
thyroid and any lymph nodes that s/he believes are involved.

The surgery will be performed within 30 days of the MRIs. The imaging results will then be
compared with the tissue that is removed during the surgery.

The thyroid and involved lymph nodes that were surgically removed will be evaluated by a
pathologist and then stored for future assessment in case the thyroid cancer recurs in the
body. This will allow the investigators to compare the kind of tumor removed at time of
first surgery to the tumor that has recurred.

Inclusion Criteria:

- Subjects must have either primary or recurrent PTC or MTC with nodal metastases
detected through physical examination and/or standard imaging techniques.

- Subjects must be deemed eligible for resection by a surgeon who is listed as an
Investigator in this study;

- Age > 18 years;

- Subjects must be willing and able to understand and sign Informed Consent.

- No uncontrolled serious medical or psychiatric illness.

- Women of childbearing potential must not be pregnant or lactating.

- Subjects will have had standard care CT, MRI, or ultrasound, and a fine-needle
aspiration biopsy demonstrating PTC or MTC with nodal metastases or
recurrent/persistent nodal disease in a patient with known PTC or MTC.

Exclusion Criteria:

- Subjects who have a known allergy to iron;

- Subjects who are pregnant or lactating;

- Subjects who are less than 18 year of age;

- Subjects with a counter-indication to MRI, such as the presence of metallic
prostheses or implanted metal device (e.g., infusion pump, defibrillator)

- Subjects with sickle cell disease, hemoglobinopathy, hemochromatosis or other
clinical conditions that may lead to iron overload.

- State a medical or scientific reason if women who are pregnant or nursing will be
excluded from the study. Guidelines and procedures pertinent to this requirement are
available at: http://ctep.cancer.gov/protocolDevelopment/templates_applications.htm.
Suggested text is provided below and may be modified as necessary.

Pregnant women are excluded from this study because there are no studies of ferumoxytol in
pregnant women. In animal studies, ferumoxytol caused decreased fetal weights and fetal
malformations at maternally toxic doses of 13-15 times the human dose. It is unknown if
ferumoxytol is present in human milk. Because of the potential for adverse events in
nursing infants, a decision should be made whether to discontinue nursing or to avoid
ferumoxytol.

- State a medical or scientific reason if participants who are cancer survivors or those
who are HIV positive will be excluded from the study. The full text of the Policies,
Guidelines, and Procedures pertinent to this requirement is available at
http://ctep.cancer.gov/protocolDevelopment/templates_applications.htm.

Individuals with a history of a different malignancy are ineligible except for the
following circumstances. Individuals with a history of other malignancies are eligible if
they have been disease-free for at least 5 years and are deemed by the investigator to be
at low risk for recurrence of that malignancy.

HIV-positive individuals on combination antiretroviral therapy are ineligible because of
the potential for pharmacokinetic interactions with ferumoxytol and the propensity to have
inflammatory adenopathy.

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