Asians, women, non-smokers, and those with adenocarcinoma histology. This drug still has been found to benefit males, smokers, and those with squamous cell histology, but to a lesser extent.
m doing research as quickly as I can to help she and her husband make an informed decision about what to do...if anything. The local drs are recommending 4 weeks of full brain radiation followed by tarceva. Prior to the finding the mets, they were planning 6 weeks of radiation to the right lung in combination with etoposide and cisplatin.
I'd appreciate any feedback. My thanks in advance to all responses....
Thanks for your response. To clarify: his treatment was adjunctive. At the time they saw no sign of cancer outside the lung. Now, however, after 4 rounds of chemotherapy the disease seems to have spread during treatment with taxotere and cisplatin: it's now in the liver, bones and adrenal glands. His original tumor was EGFR positive that is why Tarceva came up as a viable second step.
She has done very well with chemo and radiation until recently. She was started on Tarceva about 3 weeks ago. Recently, she has been experiencing a lot of confusion. I cannot find anywhere that this is a side effect of Tarceva (it is the only drug she is on at this time). Is it possible that she has a brain metastases? If not, what are the likely causes.
Radiation is usually advised for patients who are not fit to undergo an operation. The key words here are selected (selected patients) and individualized (individualized approach). This highlights the fact that there is an advantage, but the intervention is not for everybody.
The decision is not simply, let’s do it, there is an evaluation about how much lung to be removed and whether or not it can be tolerated.
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.. no surgery/ no chemo/ no radiation.
-\ Anyway, its nice to know i have people out there who really care. I wish there was one of these sites for cancer patients. There probably is but im rarely on the computer. If any of you all are interested, my sister put up a website for me called Gina's Angels. It talks about how im doing and shows pictures and stuff. Id love for you to check it out and maybe "like" the page on fb. My love to all of you!
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.
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....
Hi There...
I have had a upper right lobectomy on Sept 14 2001.Stage 1A BAC lung cancer...no chemo or no radiation..clear margins and no lymph node involvement.. ..it's been a little over five years now. cancer free. PRAISE GOD...and thou I realize that 5 yrs is maybe the magic number for most lung cancer survivor's...is it also meant for BAC Lung Cancer...I have heard not so....
Thank you for any information you can give me....
i was diagnosed with myxedema coma in july of 2009 and would like to know how long it took for most to get better. I was in the icu for 3 weeks sent to a nursing home for a month and sent home with a whole crew of help. I lost my short term memory my speach which the memory has returned my speach is clear but not my normal pitch and i now need surgery to correct that..im still not walking.
The importance is that by and large, 2 drugs are recommended for patients who are deemed well enough to aim for extending survival. You asked in the other post about the chances of making it til June, if she is receiving only 1 drug, and is pretty much in bed more than half of her waking hours - the goal of treatment may be to improve symptom control - not really halting cancer progression. If this is the case, her chances would be less.
Stay positive.
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