Anyone taking Tagrisso for Lung Cancer?
Is There anyone taking Tagrisso And feeling well on it. I’m taking 40 mg of Tagrisso I have a little bit of Dizziness. I was on 80 mg but I developed a lot of bruising on my legs so my doctor put me On 40 mg. Is this a good drug?
Thank you so much,
Barbara
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@codym, oncologists are divided on this issue of discontinuing Tagrisso. I've been on it for over four years and have a friend who has been on it for over seven. Our oncologists both feel that as long as it's working, they will keep using it, which makes sense to me. Why stop a treatment that's working?
If you want to stay current on the latest research, join the International Association for the Study of Lung Cancer at iaslc.org. It's the world's most extensive collection of thoracic oncologists, radiologists, etc., and is over 50 years old. You qualify for a free membership as a lung cancer survivor. They have hundreds of educational courses, podcasts, and simulations available online. Plus, once you're on their email list, you'll get announcements of the latest studies describing what's working today. Total disclosure: I'm not only a member but also a patient research advocate and advise researchers on the patient/caregiver/community perspective.
My oncologist and my current plan is to switch to Amivantamab and Lazertinib if and when Tagrisso stops working. You should also know that this is our 3rd plan in the last 3 years, as the lung cancer research community is finally getting enough funding to make regular progress and new discoveries.
So there are two good reasons not to worry! Years ago, I decided I would not live as if I knew the expiration date because that's no way to live. For the most part, I'm able to live my life with no thought of lung cancer at all. I highly recommend it!
I was told that I can't take any immunotherapy drugs after my adverse reaction to Tagrisso. I am now a "wait & see" I have pet scan next week to see if there's anything new or my cancer is stable. Terrible way to live
Tagrisso is an amazing drug from my experience. I have EGFR NSCLC and have been on Tagrisso for about 1 1/2 years. There is a Facebook page called EGFR resisters that is a good support group. Good luck.
That’s NSCLC - non small cell lung cancer. Sorry, typo.
@nanajan, hmmm, I don't see the relationship. Tagrisso is a small molecule targeted therapy that enters a target cell and directly interferes with the cancer's efforts to make that a cancerous cell. It has no relationship with your immune system. But then again, I'm not an oncologist.
I've had lung cancer for six and a half years, metastatic for over four. I choose not to let the numbers determine my life but, instead, to live with hope, determination, and optimism. I encourage you to join me in living with hope, determination, and optimism, not just in health but in every challenge you face in life.
Hi Matthew - I was diagnosed almost a year ago did four rounds of chemo and then they got the results back that I had the EFGR Exxon-21 mutation which I believe is what you have. I have bern on Tagrisso since April.
I’ve and pretty unfortunate with the side effects pretty much just the diarrhea.
You kind of forget you have cancer when the medication‘s working and you’re feeling fine then every now and again it enters your mind.
Thanks for all your post. They’re really helpful.
Thank you for the kind words. I have the Exon 19 mutation which is also treated with Tagrisso.
You're right about pretty much forgetting you have cancer when the medication's working and you're feeling fine! It's not my current condition, but I remember, and I'm looking forward to that "no significant side effects" state again!
May I ask your current condition?
Hi - is your cancer staying under control with the Tagrisso?
Sorry I shouldn’t have asked that I’m assuming that you’re on that other plan that you and your doctor had?
I know my doctor reminds me that the medicine will stop working at some point.
Gotta love the optimism!!