Capivasertib and fulvestrant injection
Hi All, just about to start this treatment and was wondering if there is anyone already on this combo and could share their experience with me.
Thanks in advance 😊
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Hi and welcome @love178newport!
We're so sorry for the reasons that bring you here, but we're really glad you've found us. You're sure to find our community a wonderful source of advice, information, encouragement, and support — we're all here for you!
We're hoping others will weigh in soon with their experience with capivasertib (aka Truqap). In the meantime, you may want to check out the Truqap for MBC thread and introduce yourself, share your story, and ask your questions — we're sure you'll find that thread helpful.
Also, we wanted to invite you to join one of our free weekly MBC virtual support groups where you can talk with others who are on this treatment. You can see the schedule and register here:
We hope this helps and that you get the support you need soon! Let us know if there's anything else we can do to help!
—The Mods
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Thank you so much for your welcome, I will look into the thread you suggested.
It helps knowing there is support out there 💖
Kind Regards 🙂
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I am starting next week capivasertib and fulvestrant i think same regimen
Please let me know how you are doing as you are a bit ahead of me.😊
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I am starting this as second line as well, on Wednesday. I came to get insights, but it appears that there are so many mentions of one of the drugs but not both. Perhaps we need to take a little dive into these as well. Hoping things go well for us both 💪👍
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Any updates?
My oncologist is looking to move me on these meds as a second line of therapy. I was on Kisqali and Letrozole. Unfortunately, my tumor markers are elevating slightly (0.1, 0.3 and now 5.34) and the last PET showed brightness over the left liver lobe (where they did a biopsy, found negative, a couple months ago… even though I am fairly certain that the biopsy is the cause of the brightness over the liver (it was PAINFUL and still hurts from time to time), the elevating tumor markers have me thinking a move to the next line of therapy is a good decision).
I heard placing ice on the Fulvestrant injection location for about 5-10 minutes before injection, slow administration and warming the medication in the hands for a couple of minutes prior to injection help with the pain. I also heard ice on the injections site as well as heat (turning on seat warmers in car) can help.
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Hi minnie 22 and love 178
I just began capivasertib and fulvestrant the needle was not painful and day one of capivasertib and i feel good. All the best on your experience and hope it is effective and easy!
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Hi. I started as planned as well. So 4 days done and I have not experienced anything out of the ordinary. Maybe a little more tender buttocks, but that lasted maybe two days. The injections went well, without any prep on my part. But, I had made myself so nervous reading about it I think my anxiety got the worst of me and I almost fainted during the first injection. The nurse was so kind, and she got a chair under me in time to avoid catastrophe. What a whimp 😊 After all the needles and biopsies and indignities we go through, who knew this would bring me down. Anyway, all good. She got the full injection in, and I got my second one while reclining on my side. On my drive home I did put on my car heater as well as the seats. And I took my exercise class in the evening because I read one should keep active, and had no issues.
in terms of the Capivasertib, I went through my first four days and things seem fine 🤞Not sure about you, but my MO prescribed me Claritin and I take it every morning with the Capivasertib. Maybe that is the ticket to avoiding some of the rash and itchiness. I don’t know, but I haven’t needed to take any of the other drugs associated with the other side effects. Oh, and I’ve seen a dietician at diabetes clinic and she showed me how to take my blood glucose levels. So, it seems that my doc has everything taken care of, and I hope I continue to tolerate things. Obviously I want to see a reduction in my liver met ( ultrasound in July will show that) but I think that is likely given the research. It is just if the body allows the drugs to do their job.
I hope your treatments proceeds without I’ll effect as well. 🤞please continue to update, as will I.
Happy Mother’s Day if it applies. Not to me, so heading out now to take my 95 year old Mom out to breakfast. 🌻🪻1 -
been in it for a month. No rash yet and just the runs that I have to take an Imodium for occasionally. I have some fatigue but daily exercise like walking fitness and yoga classes helps. It’s my third line so I’m always a bit fatigued while on any med anymore, but staying active, drinking water, avoiding as much stress as possible (not easy) and caring for myself helps.
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Hi all,
I had my first injections on 5/15. I used ice packs and put lidocaine cream on prior to injections (very messy, even with trying to cover with plastic wrap! I plan on buying and trying the over-the-counter patches). I felt the one injection more then the other… the nurse said it was likely bc that side had a chance to warm up from my sitting on the ice pack? Anyway, ironically, the side that didn't hurt still sometimes feels like there is a knot of pain at the injection site. I was told to massage the locations to work out the knots; I have rubbed them some.
I experienced nausea within the first couple of days, mainly after getting out of a moving car. The anti-nausea melts have helped with that. My major "ugh" is the bone pain! It isn't always there/noticeable. But when it shows up, it is very painful! One night, about one week after the injections, the pain was so bad I couldn't sleep! I had to take 3 ibuprofen, compared to the occasional 1 I usually take to ward off pain.
I am hoping the bone pain improves as my body gets used to the medication. I will be adding the Capivasertib sometime in early July, after 3 cycles of the Fulvestrant.
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Hi there. Well I’ve finished my three loading doses of fulvestrant, all okay on that front, and now every 28 days, yahoo. After telling the nurse and MO about issues I’ve been experiencing - mainly digestion and bad fatigue- they concluded it was the Capivasertib, and the decision was made to lower my dose. I had started with the middle dosage, so am now on the lowest, and that is 200mgs twice daily. I still take it with Claritin. The studies on PFS did not separate results by dose, so the advantage it gives is unknown, but the total was an average anyway. I hope these SEs stop with this change, otherwise I’ll ask to go fulvestrant only.
hope everyone is doing well ???😶 sorry for the late post, I don’t get notifications for the group it appears.0
