How are people with liver mets doing?
Comments
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Susan, that is fantastic! Thanks for making my day.
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Susan - That is so phenomenal! Happy for you! Hope you get to celebrate!
Sadiesservant - Yes, bring those trials on!
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Thanks to you all for your kind messages!
Hugs, Susan
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Dear Susan, amazing news, we celebrate with you! Saulius
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yay susa
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Thanks LFF!
I realized that I sent out the wrong trial link. They started a Phase 2 trial for HER2+ only. I am HER2 2+, equivocal. The trial I am on is Phase 1 and enrolling HER2 3+ and HER2 2+ patients.
Here's the link to the trial:
https://clinicaltrials.gov/ct2/show/NCT03255070
Hugs, Susan
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SUSAN YES!!!!!!!!!! I am sooo sooo sooo happy for you!!!!!!
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Thanks Nicole!
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Well I am getting nervous now... everytime after I eat now..I am nauseous......I am worried that there is cancer in my stomach or pancreas or something....I have NEVER had nausea after eating....ever. Any ideas...?
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Dear all, thanks for replying to my question about my mum's cyberknife marking procedure. It was way less painful and way less traumatic for her than the biopsy and she recovered quickly. Tomorrow she starts treatment finally.
I am so happy that at least American women can get into trials and try all the amazing new meds. Sadly, my mom doesn't have that opportunity but I'm hoping she will continue to have stable disease.
Nicole, fullness and nausea is quite common with liver mets from what I'm informed. Also, nausea is common with cancer treatment as you already know. Talk to your oncologist and try to stay calm.
Sending hugs to all
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Thanks Daughter...yea I know that but my liver mets have never caused that...I am thinking I definitely have some GERD/Acid reflux going on....
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Nicole, it's entirely possible that with a new drug, comes new side effects, and that it doesn't mean the drug is failing or that cancer has spread.
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Thanks Husband...I needed to be reminded of that
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Consider talking to both your oncologist and your GP about managing the side effects. My wife got no where with her oncologist, and now is getting some relief from cramping and stomach pain from her GP. He prescribed her some sort of GI tract relaxant, and its working very well, but she had to take it 3-5 x a day. But the point is, it took her GP to get her help, and her Onc wasn't really interested in finding a solution. It seems they don't consider it their job.
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Nicole,
I take lorazepam (Ativan) two times a day to help with nausea. I now that others use things like ginger, but I cannot stand the taste of ginger anything -- Ativan isn't generally used for nausea, but it works for me and it also has a calming (though not sedative) effect with respect to my anxiety.
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Thanks Husband and Bev ... Bev I do have Ativan... I felt better eventually but took Pepcid...I just ate dinner it wasn't anything spicy so I am waiting to see if I have nausea again.
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Nicole,
I take Pepcid too, every day. I think it helps some, so hopefully that will do the trick for you.
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I rarely get nauseous but when I feel it coming on, I take Compazine. I also took it as a premed. Theresa gave me this advice: "I was prescribed 10mg of Compazine to be taken up to every 6 hours and took 5mg at a time, once or twice a day which helped I also took a very small dose of olanzapine at bedtime (1.25mg) which seemed to help significantly." I miss her so much.
Once in a while, I regurgitate a small amount of fluid from my stomach. Kind of like a mini vomit. So nasty. Would appreciate helpful hints about how to. handle that.
Hugs, Susan
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Hello, I had GERD long before dx Mets IV. I’ve been on different meds as I would build up immunity then change. I take Nexium now every morning. Good luck in getting help. Be
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For those on Ibrance and other CDK4/6 inhibitors beware of proton pump inhibitors for controling GERD, nausea and other gastrointestinal problems. There's a study showing that these meds decrease the efficiency of CDK4/6 inhibitors. Someone linked the study earlier.
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Yes, and I'm not sure that all MOs are aware of this or give it much credence. I brought this to my doc's attention, but unfortunately, the study was released after I was deemed to have "failed" on Ibrance.
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More research is definitely needed but better safe than sorry.
My mum finished 3 cyberknife sessions and is to continue being on Ibrance. Ibrance kept her smaller mets stable but the two largest kept slowly increasing. Hopefully now dead from cyber!
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The new tablets are supposed to prevent the PPI problem that the capsules suffered from. From Pfizer's website:
Any chance the study you are referring to, was conducted using the old format, capsules?
Gastric pH Elevating Medications:
Capsules: Data from a study in healthy subjects indicated that coadministration of a single 125 mg IBRANCE capsule with multiple doses of the PPI rabeprazole under fed conditions decreased palbociclib Cmax by 41%, but had limited impact on AUCinf (13% decrease) compared with a single 125 mg IBRANCE capsule administered alone. Given the reduced effect on gastric pH of H2 receptor antagonists and local antacids compared to PPIs, the effect of these classes of acid reducing agents on palbociclib exposure under fed conditions is expected to be minimal.
Data from another study in healthy subjects indicated that coadministration of a single 125 mg IBRANCE capsule with multiple doses of the PPI rabeprazole under fasted conditions decreased palbociclib AUCinf and Cmax by 62% and 80%, respectively, when compared with a single 125 mg IBRANCE capsule administered alone.
IBRANCE capsules should be taken with food.
Tablets: Data from a study in healthy subjects indicated that coadministration of a single 125 mg IBRANCE tablet with multiple doses of the PPI rabeprazole under fasted conditions had no effect on the rate and extent of absorption of palbociclib when compared to a single 125 mg IBRANCE tablet administered alone. The effect of coadministration of a single 125 mg IBRANCE tablet with multiple doses of the PPI rabeprazole under fed conditions have not been evaluated in clinical studies.
Given the reduced effect on gastric pH of H2 receptor antagonists and local antacids compared to PPIs, the effect of these classes of acid reducing agents on palbociclib exposure is expected to be minimal.
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Re: Ibrance and PPI's- A lot of those studies are based on the capsules and I was explained that's why it was reccommended to take with food. When speaking to the oncology pharmacist, the tablets aren't a concern when it comes to eating or PPI's .I take PPI's 2x a day and Ibrance has been working well for me so far. Hopefully it'll remain that way. I unfortunately need to take the PPI.
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I’m off to surgery on Wednesday to get rid of a brain cyst that has continued to grow even with radiation treatment. I’ll check in but won’t be posting much in the next few days. It’s a “simple” surgery according to my team and I might be home in 2 days. It’s been 7 years since my last brain surgery that found the growth was just necrosis. There is a chance this is radiation damage but not likely. Here is to hoping. Good news is it will be gone and I will finally have a brain met to biopsy to see if my cancer has changed type. Gotta look for the silver linings.
Take care everyone.
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Update--- I had my 2nd MRI of the liver mets since starting Lynparza--- been on Lynparza for 6 months now. Still stable. No shrinkage, but no growth. Scan again in 3 months. My MO asked me again if I wanted to do Y90. I am hesitant. If the pills are working, then why rock the boat. Pain, possible complications, possible stress on liver. So I am just going to keep on the Lynparza and pray I am doing the right thing.
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Candy, that is great news.
Leftfootforward, you are in my prayers.
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Candy, Yay for stable!!
Left Foot, Best wishes for your surgery. Hope to see you back here soon
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Anyone heard from Grannax? She has not posted since Nov. Didn't someone post an update this winter, but I don't remember the response? And with this site now, it would be hard to look back (too slow to move from page to page).
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Candy - Nicole posted, in January, that Grannax had decided to stop treatment. If you search the discussion boards with her name as the keyword (not search by member name), you'll see a list of posts with her name and a short preview.
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