4 rounds of chemo of taxotere and cisplatin seem to have not worked as now he has mets in his liver, bones and adrenal glands. His doctor is aftraid that Tarceva is not recommended to someone with mets to the bone. That is not what I read. Can you please let me know if Tarceva is for him and whether that can hep stop or slow down the disease?
Thanks.
If the node is positive for cancer metastases, this may imply disease progression in spite of Tarceva intake. Tarceva may have to be replaced with another more effective chemotherapy drug. Radiation therapy to shrink the node and relieve the swelling may also have to be done. Consult with your oncologist as soon as possible so you can be properly assessed.
If the patient improves with the radiation, or maintains adequate strength or performance status(sufficient strength is usually defined as able to remain up and about at least half of the waking hours), you may wish to discuss other options aside from tarceva - such as the original plan of cisplatin and etoposide. This is because there is a known benefit for these drugs in terms of survival when used as first option among good performance status patients.
My husband was diagnosed with a Pancoast tumor on his lung. He went thru chemo/ radiation and finally had surgery to remove the tumor. It was successful. He had more chemo for precaution. After one year, the cancer came back into his Adrenal Gland. It is also in his Lymph Nodes. They put him on Tarceva( a pill he took everyday) And after 6-7 weeks, he had tests done which showed it didn't do anything.. the tumor has grown. They said there is no other options..
If you have Medicare and Medicaid, you will usually get your drugs covered by the Medicare prescription drug benefit (Part D) and the Extra Help program. Extra Help is the federal program that pays for most of the costs of Medicare drug coverage if you meet the eligibility requirements. In some limited cases, Medicaid may cover drugs that Medicare does not cover.
As long as you have Medicare Part D your drugs will be covered.
Call Medicare if you have questions.
Besides Liver Transplant Centers (where you MUST be treated to have your cirrhosis and portal hypertension managed) usually take both Medicaid and Medicare for payment so there is no advantage to Medicare. In fact Medicare is very expensive. You say you have one doctor. Any one doctor can NOT treat all of your health conditions and certainly not your liver disease. You will have to make sure the liver transplant center takes Medicaid. This should be the first think you do.
He has been through several chemo and radiation treatments and is now starting on Tarceva. It has been a long road so far and he has his good days and bad days. I don't think there's any way even the doctors can tell us how much time they have left specifically. His doctor said it could be a year, 5 or even 10, but of course we are all hoping and praying for at least 20 more with him.
I have medicare in California I will enroll in it next month,I have liver transplant with hcv and cirrhosis ,I need to find out how medicare and if medicare pay for sovaldi and olysio.
This is random i know. So i faxed over my new adress and stuff for medicare and its been literally almost a month since and still waiting for approval and i was just wondering if im not sure if i have it yet that i can just go into the hospital in the outpatient section for treatment because im literally almost 4 months preg and still have not seen a doc. even for an ultrasound for christ sake.... can somebody tell me how i can get immediate care?
It has already spread to the spine, both lungs and the lymph system. Doctors triede Tarceva for 3 weeks but her body had a very bad reaction. For the spine they did radiotherapy. But since she was diagnose 3 months ago she has lost aalmost her voice. she is using oxygen for the major part of the day but doctors don't wan't to talk about time. no more medes will be given and she was reffer to hospice....
I am close to Medicare age, and have a low viral load, so my doctor says my insurance won't cover Harvoni. Anyone know what Medicare's guidelines are? Do I have to be sympomatic to qualify? It's pretty frustrating knowing that there is now an easy cure, that I can't get. So I'm hoping the cost will come down soon, or Medicare will be more generous than my insurance!
I called Gilead and the person there told me that Gilead will NOT give any financial assistance to ANYONE on Medicare Part D. I did some research and found out that most Part D plans DO NOT cover Solvadi and even if you do get approved through an appeal, you will still be responsible for 5% of the total cost which is exceedingly high (5% of $84,000). PAN will only pay at most $7500 of this total.
Hi, My 69 year old Dad has stage 4 Lung nsc cancer that he has been battling for over 2 years with good results from first Tarceva, then Chemo and prior to that radiation to mets to his brain. He is an otherwise healthy, robust, nonsmoking person. Last month he started experiencing problems walking, nausea and headaches. He was referred to a Neurologist who recommended a Shunt to help regulate the fluid in his brain. It has been a nightmare ever since.
She is not a candidate for treatment and is refusing even palliative tx such as Tarceva. PET Scan showed no evidence of cancer in brain, liver or bone. Because she is experiencing no symptoms she is hesistant to participate in a home hospice program. What symptoms are generally experienced and if possible a general timeline for disease progression.
Oh my God! Thank you Lord for letting me hear from someone with darn near my situation!
I had lower left lobectomy May 29, 2009. Stage 1A BAC (nodule 1.3 cm)...no chemo (there seems to be only one that "might" work, Tarceva) and no radiation (what will they burn out? the lobe's gone already).
90 % "chance" of making 5 years is what they tell me. Mucho NO info on BAC. Only bad prognosis.
I have already survived breast cancer (BRCA 2 Mutation) for 6 YEARS!
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