Study on GDC0077
I am about to start study of GDC 0077. In preparation for this I have to do the following:
1-yesterday-
a-met with the study Dr to sign the forms b-had a complete eye exam
2-today-
a-had blood tests, ekg, blood pressure, weight, and urine taken
b-ct scan done
3-Next week- liver biopsy
I start the actual trial on Thursday August 10th- will keep you all informed as to what transpires. I was on Halaven but my TMs were rising like crazy so my oncologist looked into a study for me and found the one below which targets my particular mutation found during Assay Impact Testing at MSKCC. I also had a PET/CT that showed slight improvement while on Halaven (I only had 3 sessions) But my MO and I decided that I should go into the trial and if it doesn't work. I can always go back on Halaven. For me, there was no choice. My veins are shot and I needed a rest from IV chemo. Taking pills seems like an easier way to go. Plus, I am traveling a lot now so doing chemo wouldn't really work.
Comments
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Babs, Thank you for starting this thread to document the steps you are taking as you prepare for the trial as well as your experiences once the trial begins. It sounds like you are busy already. I hope the treatments prove to be effective for you and others. It takes a special person to participate in a clinical trial, and I appreciate you and others who are doing it. I look forward to reading your updates. In the meantime, enjoy your trips.
Hugs and prayers, Lynne
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Agreed. Thanks for the thread, I'll be following it and sending good vibes your way.
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Hi Babs,
We are here to cheer you on!! As we have discussed on earlier threads, the PI3K mutations are the most common mutation that crops up as breast cancer become resistant to any of various therapies. But the problem has been to get an inhibitor that works better and with far fewer side effects than a drug like Affinitor. Your trial will test a new PI3K alpha-subunit specific inhibitor, alone or with Ibrance-Femara.
I don't see much info out about this new drug, other than a short report that just came out last month:
A structure-, property-, and phenotype-guided strategy directed at high PI3K-isoform and PIKK-family selectivity, as well as a distinct cellular mechanism of action, culminated in the discovery of GDC-0077. Differences in primary and tertiary structure among PI3K isoforms were leveraged to achieve >300-fold selective inhibition of the PI3Kα isoform over the β, δ, and γ isoforms in biochemical assays. Very high selectivity over PIKK-family proteins such as mTOR, DNA-PK and VPS34 was also achieved through this process. In vitro and in vivo data indicate that GDC-0077 operates by a mechanism that promotes the selective degradation of "hotspot" p110α mutants (H1047R, E545K). Treatment of nude mice bearing PIK3CA-mutant breast tumor xenografts with oral GDC-0077 resulted in tumor regressions at well-tolerated doses. Together, the high degree of isoform selectivity, selective degradation of mutant-p110α, and in vivo PK/efficacy support the clinical evaluation of GDC-0077 as a treatment for patients with locally advanced or metastatic, PIK3CA-mutant cancer.
Basically, this drug is supposed to go in and degrade the mutant PI3K that is driving your cancer cell growth. As with all drugs, the cancer will eventually find a way to mutate some other protein and keep growing, however the stronger the drug, and hopefully the benefit of combining it with other drugs like Ibrance, will beat it back for a very long time. Best of luck and we are all with you!
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Thank you for sharing Babs. I am at the point where my Dr says is the best time to be looking for trials, So I have been since spring but nothing has come up that I have been qualified for. I am on month two of Kisquli, but even though its too early to see if its working, my tumor markers keep rising and I have had every side effect possible. (Ibrance was a dream, my Dr says this is similar but my body doesn't think so!)
I'll see if I have this mutation, I know my Foundation One report didn't come back with much that was "helpful" but I will have to investigate further.
Hugs
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Cheering you on and sending great hopes for the efficacy and tolerability of this trial for yo
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Hi Babs, thanks for starting this thread and for participating in this trial. I'll be watching closely and cheering you on all the way!!
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following. cheering.
Z
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Hi
Waiting to be taken in for liver biopsy. The trial requires a fresh sample before starting the treatment and another one when a patient leaves the trial. This is my 3 rd liver biopsy!!!! Ugh!!!!
Bab
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Ugh! I am sorry you have to go through yet another liver biopsy. Nine more days until the trial starts, right? I am keeping you in my thoughts and prayers.
Hugs, Lynne
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So glad I did the biopsy. IR thinks I'm a great candidate for Y90 if the trial doesn't work. He contacted my MO about it That's a plus. !!
In recovery and I'm soooo hungry!
Bab
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hey Babs, I did a GDC trial last summer at MSKCC, in combination with Femara. I was fortunate to have a skin met, which is easier to biopsy twice, under the trial protocol. Unfortunately the dermatologist who did the biopsy created a huge scar directly under my left arm that's very visible now. A martyr for the cause. ;-)
I wish you the very best during the trial. Hope you feel fine and have good results.
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Good luck with the trial, Babs. And a candidate for Y90? That is excellent news!
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Hi Ronda. What was your experience in the trial? Was it for the sane mutation as this trial?
Bab
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Today's day 1 of trial. Will post at end of the day!
Babs
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Hi Babs, Good luck. I am thinking about you. I can't wait to read about your experience on day 1.
Lynne
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I will be thinking of you today, Babs! And, I look forward to following your progress. Hope today is a good day!
Oriole
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Hi Babs - thinking of you and wishing great success on this trial!
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Thank you all!!!!
Here's hoping this study works-its a major time commitment. I still work FT hood thing I have a supportive boss!
Went to MSKCC without eating or drinking anything since the night before
8:30. Took weight, finger stick, EKG, temp and blood pressure
9:00 Met with my MO then study nurse. Took my GDC0077 and Letrozole at 9:48. Nurse went over all the protocol, gave me a diary to keep, and gave me a cold pack for the GDC0077. It must be refrigerated. Am not allowed to eat until 3 hrs after taking the meds.
1018. Must have many vials of blood taken about 1/2 hr after taking the pills. Of course my veins had an issue so I'm a little black and blue now. Also took temp and blood pressure.
11:48 ekg
12:48 temp blood pressure and lots more blood drawn
I can eat now. I was soooo hungry and thirsty. Lucky for me I live 1 1/2 blocks from Mskcc so I went home. I actually fell asleep! Guess I didn't sleep that well last night due to being anxious about today.
3:48 temp blood pressure and more blood taken. Glad the needle is finally out of my arm!
5:48 ekg. And all leads removed
Long day but unlike most I can go home in between so it's easier for me
Tomorrow I report at anywhere from 9:18-10:18. on an empty stomach again There is a 1/2 hr window before or after the initial time pills are taken for every part of the day
The worst part of the day for me was the blood draws. Even though they left everything in all day they did have trouble getting the blood to flow so they had to manipulate the needle. Ouch!!!
Will report on tomorrow!
Babs
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Wow, Babs, What a crazy day. You must be exhausted. It is a nice benefit to live close to the hospital. Relaxing at home is so much easier than relaxing in a hospital. The fact that you weren't allowed to drink for so long probably didn't help during the blood draws. A little hydration can work wonders. I hope you are able to sleep better tonight. Thank you so much for posting for us. As you know, we will all benefit from reading about your experience.
Hugs from, Lynne
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2nd day of study
9:18 AM weight, glucose. blood pressure, temp and 2 vials of blood. EKG and then take the pills at 948. Can eat at 1048
Now I have to take the letrozole and GDC0077 every morning on an empty stomach I can eat 1 hour later. Before I go to Israel I have to have another liver biopsy for the study!
Babs
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Go Babs!! Thanks for the detail. And doing the trial. A lot of work.
>Z<
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Just wanted to post an update.
The pills are real easy to take. But I do get a little queasy right after I do. Also, I'm no longer constipated-which is a good thing!
I have to have another liver biopsy this coming Monday as part of the study. It's supposed to be done when you've been taking the pills for 2 weeks but since I already had a trip to Israel planned for this coming Tuesday they made the decision to move it up so I could be a part of the study and still take my trip.
Will update as I have more to share!
Babs
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Babs just got to this treasure. I can't believe you have to get another biopsy and leave the next day. WOW! Interesting, so they can only see from the biopsy if something is working? Not scans? We'll keep checking on you. Thanks for this info.
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Momall-They want to compare the cancer tissue from before the study, 2 weeks into and then again at the end. That's in addition to scans- that's really how they see if it's working.
Went yesterday for the study again-temp, blood pressure glucose, weight and 4 vials of blood and then meeting with the study nurses. Monday is the liver biopsy and then Tuesday another appointment- so much time for this!
Babs
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Today is another liver biopsy Waiting now to be taken.
Bab
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Biopsy is over. The hardest part was getting the IV in. IR had to do it via ultrasound. But I am fully black and blue yet again
Baba
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Today's visit they did glucose weight blood pressure, temperature oxygen level ekg and 9 vials of blood
Next saw mo nurse and study nurse.
All is good. Leaving for Israel for 2 weeks tonight
Bab
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Have a great trip! Try to take a vacation from cancer and not think about it!
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Animal Crack i intend to totally forget that I'm a cancer patient. My veins really need this rest too! Plus I want to enjoy every minute with my DD and SIL. How lucky am I that they want to spend their vacation with me!
Bab
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They are also the lucky ones! They get to spend this time with you! Have a wonderful time! Wishing you nothing but joy!
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