Would love to hear of experiences treating lymphovascular invasion

Posted by davebross @davebross, Mar 12 9:04am

I would love to hear of anyone's experience treating lympho vascular invasion. My surgery to remove stage 3 tumor (5.5 cm) was successful. Clear margins and no malignancy in 43 lymph nodes. I'm waiting to meet with oncologist, but want to research options/prepare myself. Thanks, in advance!

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Back in 2013 when I was first diagnosed with co-rectal cancer I took treatment first before the APR surgery . Etopiside and Cisplatin along with radiation treatments at the same time. After the treatments a year later it came back . Taking chemo and radiation at the same time was rough but I got through it. After it came back I had APR surgery 7 lymph nodes were removed at that time of surgery 3 of those 7 lymph nodes had cancer cells in them and it matasis to lungs . I was started on opdivo and Yervoy but the side effects to those two immunotherapy gave me an allergic reaction . They were discontinued and the put my on keytruda and I have been on Keytruda ever since. I didn't have no hair loss with keytruda , no nausea just dry mouth. A dose every two weeks for several weeks till you go in remission then it's stopped and Pet scan every 3 months . When I come out of remission keytruda is started back up and so is radiation treatments

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Thank you for sharing! So it sounds like management with immunotherapy. Have they used ctDNA for management?

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@davebross

Thank you for sharing! So it sounds like management with immunotherapy. Have they used ctDNA for management?

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Yes, they have.

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CTDNA has advanced significantly just in the past 6 six months. Although the currently utilized Guardant ctDNA has great benefit, and is leaps and bounds ahead of CEA, a new ctDNA test, which is made (informed) by your own tumor cells, SIGNATERA, if far better. And can inform the doctor of the existence of recurring cancer a full 9 months before a CT can pick it up. Ask your oncologist about this new test. It is covered by Medicare and insurance

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Would you happen to know why it's better than the Guardant test? Unfortunately United health care doesn't cover it, but I may appeal. Thanks for the recommendation.

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@davebross, have you met with your oncologist in the meantime? What are next steps for you?

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Thanks for asking. We meet tomorrow. Based on my research, anticipating Folfox regimen, either 8 or 16 weeks.

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@roywalton

CTDNA has advanced significantly just in the past 6 six months. Although the currently utilized Guardant ctDNA has great benefit, and is leaps and bounds ahead of CEA, a new ctDNA test, which is made (informed) by your own tumor cells, SIGNATERA, if far better. And can inform the doctor of the existence of recurring cancer a full 9 months before a CT can pick it up. Ask your oncologist about this new test. It is covered by Medicare and insurance

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@roywalton, @davebross
The Signatera test is not currently covered by any insurance, so even thought they send a bill, they don’t expect payment. They are covering the cost themselves for the time being. So there is no cost to the patient at all.
I recently had my test for the bio markers and genetic mutations, by Altera and Empower.

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@cjay

@roywalton, @davebross
The Signatera test is not currently covered by any insurance, so even thought they send a bill, they don’t expect payment. They are covering the cost themselves for the time being. So there is no cost to the patient at all.
I recently had my test for the bio markers and genetic mutations, by Altera and Empower.

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Hi - United Healthcare/Medicare Advantage insurance is covering the cost. The firm is not performing the test at no cost

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@roywalton

Hi - United Healthcare/Medicare Advantage insurance is covering the cost. The firm is not performing the test at no cost

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They may be, but I have BCBS, and it is not covering it. And it was explained to me that most insurance does not cover it yet, and no patients are expected to pay the billing.

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