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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I’m stage I’ve too, I’m dealing also with a Holostic Dr in Connecticut. She’s detoxing me, getting rid of all heavy metals in my body. Hoping this works
Thank you. It’s 80mg. I am on stage IV, the drug works well for me except the weird lung tightness and some mild side effects. Considering only a couple of months to a year expected to live initially, I am very grateful for what Tagrisso does for me.
I’m so happy to hear that your nails and hair are doing great. That’s wonderful. Right now Tagrisso is the only meds I’m taking I take a lot of vitamins, my oncologist knows all the vitamins I take and he said they’re good. They wouldn’t interfere with Tagrisso. Thank you so much.
@babs1956, welcome to "the new normal" -- a phrase I detest in general, but in the case of our bloodwork, it's true. On Tagrisso, we'll have low red blood cell count, white blood cell count, low platelet count, low platelet volume, and low lymphocyte count (a type of white blood cell.) It's utterly normal on Tagrisso.
Also, some of us have trouble with splitting nails. Early on, I'd swear I split a nail while wearing gloves. I now take 20 mg of Biotin daily to strengthen my nails. I cleared it with my oncologist, who first assured me Biotin doesn't interact with anything else I'm taking. You should check with your oncologist before adding any meds. Now, my worst problem is that my hair and nails are growing like weeds!
I’m so sorry to hear that. Are you on 80 mg? I was getting bruises on my legs and he reduced me to 40 mg.
I have been on Tagrisso 7 months and developed some lung tightness. My doctor has no idea why, so I just totally ignore it and live a life like someone without EGFR mutation.
Also, my platelets are low. Is that bad? The number is 119.
Thank you so very much.
@babs1956, Tagrisso has been the proverbial godsend for those of us with certain types of EGFR mutation. It's a small molecule targeted therapy that has dramatically extended both PFS (progression-free survival) and OS (overall survival). My lung cancer (LC) metastasized to my brain in 2020, which is when I started Tagrisso. Four and a half years later, I'm still doing well on it and am currently cancer-free. I have two friends who have been on it for over 7 years and are both still active. One is a personal trainer!
My experience with Tagrisso is that the initial side effects, like the ever-popular diarrhea, die off after a few months. That's how long it takes the body to adapt to it. Hopefully, your side effects will also disappear over time.
The one thing I learned later that I wish I'd known early is that the most important thing is to decide what time of day to take it and then stick to that time to maintain a constant level of the drug in your body. Initially, I chose two hours after breakfast and two hours before lunch, and that's still when I take it. Consistent time is more critical with some people than with others, but it turned out I'm one of those people. I had a slight recurrence about a year ago that we successfully treated with 1 round of targeted radiation. My friend Larry had a similar experience. Neither of us has had any other recurrence since the first one.
Targeted therapy is the future of lung cancer treatment; new ones are being developed almost daily! It's actually a challenge to keep up with them all. You can learn more at lungevity.com, go2.org, and, if you're ready for a deep dive, you can join the International Association for the Study of Lung Cancer and see the same information your oncologist is reviewing. Lungevity and GO2 are much more user-friendly. 🙂
Welcome to the club no one wants to belong to, where there are more of us living our lives with lung cancer than ever before.