Hope for those wanting to get on Palbociclib (Ibrance)
I found out a couple of days ago that my insurance (Regence Blue Cross Blue Shield) is going to cover Ibrance for me. I was very surprised, because, while I meet most of the requirements to receive this drug, I have had endocrine therapy, and so I assumed I would get denied by insurance, even though my oncologist recommended it for me. I was looking into alternative routes to get access to Ibrance (Palbociclib), but we ran it through insurance first. I think my oncologist did a good job of making the case that it was the right drug for me, and I got approved!
I am really happy about this, and wanted to share with any of you who are hoping to get on this drug. I also heard from a friend in Michigan who has MBC who was also approved. She similarly did not know if she would qualify. I don't know what insurance she has, but I think this is promising news. My hospital doesn't have the drug in stock yet, but I should be able to get on it fairly soon. Any other successes with getting insurance approval for Palbociclib out there?
Comments
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This is very promising, thank you Springlakegirl. What state are you in? I know that each state has their own system, even within insurers, so it may help others to know. I'm in California, and I do think there are people in CA who may be in line to get it as well.
What are you taking it with? Are you just adding it to your current hormonal, or is your onc switching you to a different one? Good luck!
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Sandilee, I am in Utah, and my friend is in Michigan. Both of us felt like our oncologists really made the case for us with the insurance companies, so maybe that helped. I don't know.
I will be taking it with Letrozole. I am currently on Tamoxefin, and it seems to be working just fine for me, but I have been trying to get on Palbo/Letrozole for several months now (through the phase 3 trial they had, and now through insurance), and I feel good about this option for me right now. My hope is that it will be available to those who feel that it is the right fit for them right now. I know there are a lot of other good options out there though. But many women have been really waiting to get on this drug!
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Springlakegirl, thank you for posting this encouraging information! I hope you do very well on it!
Just a quick question if I may: if you are doing well on Tamoxifen, why might you be switching now? Just curious, as usually the protocol is to remain on a medication until it no longer works.
Best wishes!
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Bestbird, That's a good question! I was in remission for 2 years on Anastrozole, then it failed me in July 2014, and I had a recurrence in my right iliac bone. At that time, we explored all the options out there, and with my oncologist, came to the conclusion that it would be great if I could get on a trial of Palbociclib (or another CDK inhibitor).
I then went to MD Anderson in Houston for a second opinion, and without telling him what my oncologist said, he recommended the exact same thing. At that time I really came to feel at peace with that decision for my next treatment, but quickly found out it was harder to get on than I realized. I decided to stick with my decision to get on Palbociclib, but didn't want to go untreated for too long, and decided to take Tamoxifen in the interim.
When Pfizer started the expanded access program last October, I met all the requirements to get into that trial, but my hospital did not have the trial, and so they began the process of getting approved for it. According to my doctor it was the longest process, with the most hoops to jump through, that she has ever experienced, and they were still in the process of getting approved for the trial when Pfizer announced that Palbociclib was FDA approved. They would not open any new sites for the expanded access program, yet they redefined the eligibility for Palbociclib as those who had not been on any prior endocrine therapy. This seemingly excluded me.
I am a person who does a lot of research, thinking, and praying about my treatment, and then after that, I really rely on my gut feeling. So, after a recent PET scan which showed that the Tamoxifen seems to be keeping my cancer stable, I could definitely continue with Tamoxefin, but I just don't want to! That's the long answer to your short question! On paper, continuing on Tamoxifen is a reasonable option, but it's not what I feel right about, and not what I want to do. I only have one little spot of cancer right now, and I want to be on the most effective treatment that will hopefully get me back to NED, or at least keep me stable, for many years to come, and I think (and hope) Palbociclib is what will do that for me.
I was getting discouraged that my "gut feeling" was off because Palbo didn't seem to be available to me, but now I feel much more comfortable, and at peace, that I will be able to follow the treatment I feel best about.
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Springlakegirl, I'm so so happy for you! I know this was your hope to be able to take this new drug, good for you for being so persistent! Wishing you all the very best kicking that bc crap to the curb for many years
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Thank you Divine. That's my plan!!

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I started on Inrance yesterday, along with Femara. I have failed all the hormonals, but was still approved for this combo. It's being filled through specialty pharmacies. Mine was in the Los Angeles area.
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Springlakegirl, thank you for your reply! I believe there is a lot of value in having a gut feel about something and acting on it! Please accept my best wishes for years and years of NED!
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Thank you Bestbird!

Romansma, best wishes to you too!
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I will be starting on Ibrance and Femara (or you could call it Palbociclib and Letrozole) on Monday!
Hoping I still feel normal. -
Hello,
I feel much better reading the struggle stories of people like me.I was recently diagnosed for bone mets.In 2015 i got met in Bone Marrow.Now they have put me on Palbociclib and Fulvestrant.I don't know what to do.These medicines are way too expensive then I can afford.
I am from India and currently living in India which makes it even worse as It is hard to get these drugs at affordable prices here.I don't have any insurance that i can use and neither do they have any clinical trials in India that I can enrol myself for.
Confused and somewhat dejected I fail to understand what next to do.I have been fighting all this way since 2010 but not the fight gets a little more tougher.
If any of you here have any ideas about getting this highly over priced wonder drug for cheap,kindly let me know.
Last but not the least I congratulate you all for doing such a commendable job in supporting this forum.It really helps and takes your mind off it (Ca) for a moment and makes one feel good.Makes one feel that I am not alone out there.There are alot more like me,alot more who are fighting it out like me,and alot more who are confident that they will beat it one day.
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Dear Freebird, we wanted to give you a warm welcome to the BC.org forums. We are so sorry that you are going through this, but at the same time we are glad you found us and find this community a helpful source of support.
We're sorry we can't really help you with your question. You may want to contact those drugs companies to see if they have any special program in your country, or ask a social worker at your hospital or someone who can advocate on your behalf to get more support places that can offer some help.
Please stay connected here, and let us know how you're doing!
Best wishes,
The Mods
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