68Ga DOTATATE Positron Emission Tomography (PET) at Mayo Clinic

Posted by Teresa, Volunteer Mentor @hopeful33250, Jun 14, 2017

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This article regarding 68Ga DOTATATE Positron Emission Tomography (PET) comes to us from Mayo Clinic's, Dr. Ayse T. Kendi and Medical/NET oncologist Dr. Thorvardur Halfdanarson, regarding this new diagnostic tool for imaging NETs. As this is now available at Mayo Clinic, Rochester, MN, I wanted you all to be aware of it.

68Ga DOTATATE Positron Emission Tomography (PET) is the new golden standard for imaging of neuroendocrine tumors (NETs). [68Ga] DOTATATE PET has been used in Europe and Australia for the last 10 years effectively as the first line imaging choice for NETs and replaced Octreoscan years ago. Recently this imaging modality has been approved by FDA and was made available to the NET community in USA. 68Ga DOTATATE has unique ability to bind to the somatostatin receptors that are overpopulated on the cell surface of NET cells. The somatostatin receptors can serve both as a target for imaging such as Ga68 DOTATATE PET/CT imaging and the less accurate Octreoscan as well as a target for therapy, either with somatostatin analogs (octreotide and lanreotide) and radioactively tagged somatostatin analogs such as Lu-177 DOTATATE (Lutathera). Gallium is the part that acts like a light-source that is attached to the peptide (DOTATATE) which has high affinity to bind to these receptors. Once the [68Ga] DOTATATE is injected through a vein and circulates in the body for about 60 minutes, it is time to get the images. Unlike Octreoscan, you don’t need to have multiple visits to nuclear medicine. One visit for about 2 hours is all that is needed.
68Ga DOTATATE can detect more and smaller lesions than the older Octreoscans, has lower radiation and is essential for assessment for peptide receptor radionuclide therapy (PRRT). With the advent of Ga68 imaging, there is no role for Octrescans where Ga68 imaging is available. Please know that although most of NETs will light up, some won’t light up and you may need another imaging with MRI, CT or FDG-PET/CT.
Please also note that, although it is FDA approved, it is an imaging modality that is not available in every hospital or imaging center. Please make sure to ask your NET oncologist if and where you could get the imaging.
At Mayo, we have completed more than 100 cases since November 2016. As a team we are very efficient both in acquisition and interpretation of the images. We work in close collaboration of NET oncologists in our institution and most, if not all patients will be offered the opportunity to meet with a NET specialist within then Division of Medical Oncology to discuss the results of the Ga68 DOTATATE imaging study and to formulate a treatment plan going forward which also will include the use of circulating blood markers as indicated. There are now data to suggest that treatment outcomes are better for patients treated at large and specialized NET centers.

Please feel free to comment or ask any questions that you may have. I will see that your questions are answered by one of our clinicians at Mayo.

Teresa

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

@laree

Do you need a ride home after the Gallium 68 scan? Trying to prepare. Thank you

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No. I drive myself there and back.

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Do you need a ride home after the Gallium 68 scan? Trying to prepare. Thank you

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@laree

Thank you for posting all this information. I know we will have to see the Dr. to get more info. We are pretty nervous for the gallium 68 scan coming up. And when you look up life expectancy that is scary. I don't understand the stats on those. I know everyone is different. Is there anyone living long term with Pnets stage 4 to the liver currently?

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Me. 2 yrs. PNET with liver mets, stage 4. Also endometrial cancer
There is a good info from Ronny Allen - blogger about living with NET
Keep the faith!

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Me. 2.5 years since diagnosis and not only surviving, I am thriving. I am but a mere puppy compared to folks that have lived 20 years plus. Stay optimistic. It isn't always easy, but it is manageable.

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@hopeful33250

Tom: If you contact his office, they may provide it for you. Teresa

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Thank you for posting all this information. I know we will have to see the Dr. to get more info. We are pretty nervous for the gallium 68 scan coming up. And when you look up life expectancy that is scary. I don't understand the stats on those. I know everyone is different. Is there anyone living long term with Pnets stage 4 to the liver currently?

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@hopeful33250

You will probably find these NET-specific scans in research-oriented medical facilities. However, your doctor may be able to give you a referral to one of these facilities if your own hospital system does not have one.

Are you currently being seen by a NET specialist or going to a research-oriented hospital system?

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Yes, Worcester MA work with Shields who have PET/CAT G68. UMASS sends patients. Not far from New York, maybe a day trip. Blessings

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@colleenyoung

@sophiarose, your mention of heart issues tipped me off to let you know about cardio-oncology.

Mayo Clinic offers expertise in addressing heart problems (called cardio-oncology), potential or current issues. The Cardio-Oncology Clinic (https://www.mayoclinic.org/departments-centers/cardio-oncology-clinic/overview/ovc-20442193) evaluates people prior to cancer treatment and patients who have experienced side effects due their treatment.

You might wish to inquire about a consult with a cardio-oncology specialist, although it sounds like you're already in good hands. Just thought I'd make you aware of the specialty.

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Thank you Colleen
I will keep the web site you sent
So far the medication the cardiologist gave me at the hospital is working
I was suppose to see my cardiologist on Monday but that was moved to 4/1
I am holding onto hope that the issue isn’t permanent
Thank you very much

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@sophiarose

Actually after meeting with Dr Starr and his team and Lorielli I feel I would have a lot more support
I developed PVC from the Everolimus
It started in about the 7th week of treatment but by the 9th week it was full blown I was having a terrible time catching my breath my pulse was skipping and my heart was pounding out of my chest
Even though the doctors felt my irregular pulse
I had a perfect ECHO , EKG and a MRI of my heart
It wasn’t until my cardiologist sent me to the hospital and hooked up to the 24 monitor that they saw what was going on
I am on a beta blocker and it is a lot better just hoping it isn’t permanent
I will keep you posted
Thank you for your concern

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@sophiarose, your mention of heart issues tipped me off to let you know about cardio-oncology.

Mayo Clinic offers expertise in addressing heart problems (called cardio-oncology), potential or current issues. The Cardio-Oncology Clinic (https://www.mayoclinic.org/departments-centers/cardio-oncology-clinic/overview/ovc-20442193) evaluates people prior to cancer treatment and patients who have experienced side effects due their treatment.

You might wish to inquire about a consult with a cardio-oncology specialist, although it sounds like you're already in good hands. Just thought I'd make you aware of the specialty.

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@hopeful33250

Hello @sophiarose,

I am sorry to hear of the heart issue that you are having as a result of the Everolimus. If you are comfortable sharing more, I'm wondering what type of heart issue you are dealing with. I can understand that this new health issue will make this decision more difficult, especially as you consider traveling. When you said that you would have more support in Florida, is that because you have friends or family there who could help you?

You are wise to consult with your cardiologist before making a final decision. The more medical input you can obtain, the more confident you will be about what direction to take.

Will you post again after you see your cardiologist?

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Actually after meeting with Dr Starr and his team and Lorielli I feel I would have a lot more support
I developed PVC from the Everolimus
It started in about the 7th week of treatment but by the 9th week it was full blown I was having a terrible time catching my breath my pulse was skipping and my heart was pounding out of my chest
Even though the doctors felt my irregular pulse
I had a perfect ECHO , EKG and a MRI of my heart
It wasn’t until my cardiologist sent me to the hospital and hooked up to the 24 monitor that they saw what was going on
I am on a beta blocker and it is a lot better just hoping it isn’t permanent
I will keep you posted
Thank you for your concern

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