Neuroendocrine Tumor of the Lung

Jay Elsten - Neuroendocrine Tumor - Mayo Clinic
Jay Elsten - Neuroendocrine Tumor - Mayo Clinic administrator 0 Views • 2 years ago

It started subtly — no sign anything was amiss, just some itching and rashes developing on both of Jay Elsten’s legs. A trip to his primary care physician in 2012 led to an initial diagnosis of hepatitis, a prescription for antibiotics and a recommendation to call again if Jay were not feeling better in a few days.

This led to more tests, including a CT scan, and the location of a tumor on his pancreas — either adenocarcinoma or neuroendocrine — and a decision of where to go next. To learn more about neuroendocrine tumor treatment at Mayo Clinic, visit:
https://mayocl.in/36Eh9ad

To request an appointment at Mayo Clinic, visit: https://mayocl.in/2My3ZVk

The tumors’ presentation in patients is so unique that some will experience diarrhea or pain from the tumors, while others will have no symptoms and the tumors are discovered during an imaging exam for something else. Some tumors are slow-growing, others are aggressive. Neuroendocrine tumors can secrete hormones, which are the source of many of the symptoms patients experience.

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CARCINOID TUMORS OF THE LUNG (Lung Carcinoid): Signs, Symptoms, Pathology,
CARCINOID TUMORS OF THE LUNG (Lung Carcinoid): Signs, Symptoms, Pathology, administrator 3 Views • 2 years ago

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What is the survival rate for carcinoid tumor?
Typical carcinoid tumors have been found to have a much better prognosis than do the atypical variety. Atypical carcinoid tumors have been associated with a 5-year survival rate of 40-60% and a 10-year survival rate of 31-60%, depending on the series.

What are the symptoms of lung carcinoid tumors?
Signs and symptoms of carcinoid lung tumors include:
Chest pain.
Wheezing.
Shortness of breath.
Diarrhea.
Redness or a feeling of warmth in your face and neck (skin flushing)
Weight gain, particularly around the midsection and upper back.
Pink or purple marks on the skin that look like stretch marks.

#lung #tumor #carcinoid

What causes carcinoid tumor in lung?
Researchers don't really know the causes of carcinoid tumors in the lung. They have found that typical carcinoids don't seem to be linked to smoking, but atypical carcinoid tumors are found more often in people who do smoke. You may be at a higher risk for these rare tumors with: Age.

Can a lung carcinoid be benign?
Carcinoid Lung Tumor Surgery

The only effective treatment of carcinoid lung tumor is surgical resection of the primary tumor. Most tumors follow a benign course and are amenable to surgery.

How fast does a carcinoid tumor grow?
How long does it take for a carcinoid tumor to grow to the size of 2 cm? In general, it can take 3-5 years and even up to 10 or longer for carcinoid tumors to grow. These are generally very slow-growing tumors.

Are lung carcinoid tumors fatal?
The average five-year survival rate for people who have been treated for typical carcinoid tumors is 85% to 95%. People who have been treated for atypical lung carcinoids have a five-year survival rate of 50% to 60%. Survival rates tend to be higher for people with lung carcinoids that haven't spread.

Can a blood test detect carcinoid tumors?
The chromogranin A (CgA)* blood test is a good marker to help detect and monitor the activity of carcinoid tumors. This includes the tumors that release (secrete) the hormones that are associated with carcinoid syndrome. Elevated levels of CgA are found in 80% to 100% of patients with GI NET or lung NET.

Can carcinoid tumors be removed?
Surgeons often try to cure localized carcinoid tumors by removing them completely, which is usually successful. The options for GI carcinoid tumors that have spread to nearby tissues or to distant parts of the body are more complex.

Are carcinoid tumors benign or malignant?
Carcinoid tumors can be benign (non-cancerous) or malignant (cancerous). Benign carcinoid tumors are typically small and usually can be removed completely and, in most cases, they do not come back. Cells from benign carcinoid tumors do not spread to other parts of the body.

What causes a carcinoid tumor?
Most carcinoid tumors are caused by sporadic changes (mutations) in oncogenes or tumor suppressor genes. Mutations are called sporadic if they occur after a person is born, rather than having been inherited.

Do lung carcinoid tumors come back?
You may be relieved to finish treatment, but find it hard not to worry about cancer coming back. This is a very common if you've had cancer. For other people, the lung carcinoid tumors may never go away completely.

Are carcinoid tumors rare?
Carcinoid tumor is a rare type of tumor that usually grows slowly. Carcinoid tumors are cancerous, but have been called cancer in slow motion, because if you have a carcinoid tumor, you may have it for many years and never know it.

Can smoking cause carcinoid tumors?
Tobacco smoke. Typical lung carcinoid tumors do not seem to be linked with smoking or with any known chemicals in the environment or workplace. But some studies have found that atypical lung carcinoids may be more common in people who smoke.

Are carcinoid tumors hard to detect?
Carcinoid syndrome can be difficult to diagnose because the symptoms are similar to other more common conditions. Carcinoid syndrome is caused by excess serotonin and other chemicals that are secreted by tumor cells.

Does lung carcinoid cause carcinoid syndrome?
Symptoms caused by hormones from the tumor

Lung carcinoids do this far less often than gastrointestinal carcinoid tumors. Carcinoid syndrome: Rarely, lung carcinoid tumors release enough hormone-like substances into the bloodstream to cause symptoms. This causes carcinoid syndrome.

New Treatment for Neuroendocrine Tumors
New Treatment for Neuroendocrine Tumors administrator 2 Views • 2 years ago

Neuroendocrine tumors (NETS) grow in hormonal glands in the lungs, stomach, pancreas, or gut. Some produce hormones that damage your digestive system or blood sugar. Lutathera treats NETS by slowing down or stopping tumor growth.

Find out more at:
https://uvahealth.com/services..../imaging/nuclear-ima

Transcript

Matthew Reilly, MD:
One of the therapies that I use more commonly with neuroendocrine tumor patients is a class of therapies called peptide receptor radionucleotide therapy, or PRRT. Within that class, Lutathera, which is also known as lutetium 177 Lu DOTA-TATE, is an approved therapy approved in 2018 for patients with well differentiated metastatic neuroendocrine tumors.

Jeri Pugh, RN:
PRRT is used specifically for neuroendocrine cancer, also known as carcinoide cancer. And what that is is that is a cancer that develops cells in your body called neuroendocrine cells, which create hormones in the body. Essentially, it is a medication that's been specifically designed to bind to target sites on tumors, peptide receptors. And then the medication enters those cells and releases radiation over time, which then kills those tumors.

Lale Kostakoglu Shields, MD, MPH:
It gets internalized into the tumor, and allows this radiation to cause damage to tumor cell with an ultimate goal of a tumor shrinkage, control, progression. So it's a relatively highly safe treatment and effective treatment in disease control.

Matthew Reilly:
About one in five patients will see more of a response with tumor shrinkage. But for the most part, what we see is significant benefit in terms of stopping the tumor from growing, for what can be years, and overall benefit in survival.

Jeri Pugh:
So it also really improves their quality of life, as well as reduces the risk of that progressing. It turns an active progressing growing disease into more of a chronic stable disease state.

Lale Kostakoglu Shields:
Altogether, it's an eight month treatment. It consists of four cycles, separated approximately two months from one another. Patient arrives at Nuclear Medicine early in the morning. And it takes usually five hours to complete the treatment. So it's a full day out-patient treatment for each cycle.

Jeri Pugh:
The treatment itself is provided in Nuclear Medicine Clinic. So with the Nuclear Medicine radiologist, also our outstanding team of certified Nuclear Medicine technologists who actually handle the radioactive medication and provide the imaging.

Matthew Reilly:
When I take care of patients with neuroendocrine tumors, what we're often talking about is that this, unlike some cancers where we're very aggressively approaching patients with chemotherapy, we're really taking more of a longer game approach where we want to control the tumor and keep them doing well for ideally years to come.

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