How is AZEDRA administered?

Azedra is administered into a vein (intravenous). The regimen is administered in two steps; the dosimetric step, in which the therapeutic dose is determined, and the therapeutic step, where the patient actually receives the dose for treatment.

How does AZEDRA work?

It treats the whole body system, not just one body part. ▶ AZEDRA is a radiation therapy because it uses radiation to treat tumors. You can learn more about how AZEDRA works on page 12. Bone marrow problems and other cancers: Treatment with AZEDRA may cause your blood cell counts to drop (myelosuppression).

Are pheochromocytomas cancerous?

Most pheochromocytomas are benign, which means they are not cancer and do not spread to other parts of the body. Only about 10% of pheochromocytomas spread to other parts of the body.

What is Lutathera treatment?

About Lutathera Lutathera is a medication used to treat neuroendocrine tumors. It can help make the tumors grow more slowly or stop them from growing. It can also help manage symptoms caused by the tumors. Lutathera is a radioactive targeted therapy. It has 2 main parts: a radioactive part and a tumor-targeted part.

What does a pheochromocytoma headache feel like?

Characteristic symptoms accompanying headaches in cases of pheochromocytoma, include perspiration, palpitations, anxiety, and facial pallor; headaches are known to occur simultaneously with sudden blood pressure elevation [7].

Can Lutathera shrink tumors?

Lutathera treatment helps make the tumors grow more slowly, shrink, or stop them from growing altogether, and can also help manage the symptoms caused by the tumors.

How do you administer Lutathera?

LUTATHERA must not be administered as an intravenous bolus. Use a clamp or pump to regulate the flow of the sodium chloride solution via the short needle into the LUTATHERA vial at a rate of 50 mL/hour to 100 mL/hour for 5 to 10 minutes and then 200 mL/hour to 300 mL/hour for an additional 25 to 30 minutes.

What triggers pheochromocytoma?

Pheochromocytomas/paragangliomas may be caused by mutations of one of at least ten different genes: the RET gene, which is also associated with multiple endocrine neoplasia type 2; the VHL gene, which is also associated with von Hippel-Lindau syndrome; the neurofibromatosis (NF1) gene, associated with neurofibromatosis …

Can you drink with pheochromocytoma?

You shouldn’t drink alcohol or caffeine or take amphetamines, benzodiazepines, certain antidepressants, or lithium when doing the test. These substances may lead to false high levels. Magnetic resonance imaging (MRI), CT, and other scans may be done to look for the tumor.

Does anxiety cause pheochromocytoma?

Anxiety and panic disorder may be the main presenting symptoms of pheochromocytoma. The diagnosis of pheochromocytoma should be excluded in cases of long-term panic disorder refractory to medications since the anxiety may be secondary to a catecholamine-secreting tumor.