Taxol v Abraxane (Early Stage)
Hi guys
Just wanted to ask your opinion on the 2 chemo options above.
I know Abraxane is often saved for 2nd line treatment - when Locally Advanced or Mets have occured.
But if given during 1st line treatment (instead of Taxol), does this not DECREASE the chance of Mets occuring?
After all, Abraxane is just Taxol, but in a more efficient form - delivering more of the active ingredients without as much toxicity.
Any thoughts/experiences?
Comments
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I had taxol. I asked about using Abraxane but honestly I can not remember why it wasn't an option. Thats kind of sad that I can't remember. It must be from the taxol...just kidding. I would be interested in hearing from someone who did have it.
Teresa
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Good question. I don't know! I'm set to start chemo on 2/5 and will have dose dense AC+Avastin for 4 cycles and then T+Avastin for 4 cycles.
Seems like the "standard" is DD AC+T or TAC currently. At least, that's what the 2 onc's I saw both said.
Michele
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Abraxane does not stop mets, it "treats them" I think this is the key to this chemo.. Best response seems to be in the lung and liver. If you do not have these kinds of mets it doesn't really help you.
With early stage disease there are still standards...they may change a little but not a lot. Michele you are in the protocol other want because you are receiving Avastin with early stage disease.
Another key to remember with chemo is...If your disease returns after treatment the tumor becomes stronger and smarter. They want to have the stronger and smarter chemo on hand to treat them. With early disease your tumor is not very smart yet, so they feel they can out smart it without using all the big guns. Not that "A" not a big gun...it is. But they just will not move off it as first line one treatment for all kinds of bc. My onc. feels Ixempra in five years or so, will be the first line of treatment. It's a tough drug like "A" but show a lot of promise for many TN.
Flalady
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Floridalady
I am using carboplantin for early stage. (My tumor was 1 cm and had 1 mm micro mets in one sentinal node.). Do you think it is too much of a big gun to use carboplantin? I wanted to treat it as aggressive as possible so that I have the best chance to avoid recurrence.
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Nope! newalex... Carbo is consider a gentle chemo. But does work for many TN ladies. My 2nd group of chemo had Carbo. It did work for about six months on my aggressive tumors. I think it is good mix for your treatment.
Flalady
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Michele,
I had avastin with my treatments as well (clinical trial e5103)
Teresa
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I had Abraxane instead of taxol as a first line treatment for early stage triple negative breast cancer as part of a clinical trial (as well as AC and Avastin). Abraxane is crazy expensive, so it may be hard to get outside of a trial. But if you can get it, I think it's a good idea.
From what I understand, Abraxane should be at least as effective as taxol, possibly more so due to the way that nanoparticle drug carriers (like Abraxane) preferentially accumulate in tumor beds. I have also seen some articles saying that triple negative cancers tend to overexpress the CAV1 gene. Apparantly, Abraxane preferentially targets CAV1 whereas taxol does not, so it could be particularly beneficial to triple negative patients.
Also, you get to avoid all the steroids and premeds that are needed to tolerate taxol if you take abraxane instead. Of course it still has nasty side effects like most chemo, but in my case it wasn't that bad. I was already bald from AC, so my main complaint was aches in my legs that were pretty intense for several days each cycle then faded away a few days before the next treatment. I didn't get neuropathy, but I think that may be more common with Abraxane than taxol if I remember correctly.
Triple negative cancers are quite aggresive. In my humble opinion, it is best to attack them with whatever ammunition you have access to the first time around to hopefully prevent a recurrence.
Best wishes,
Chloe
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Chloe,
I curious what was the finding in the trial? Was there any proof this worked any better than other Taxol family of drugs?
Flalady
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From this site. I'm looking to see if the finished the trial. All I can find is where the stock went up with the news they were going to start the trial. $$$$
Generosa Grana, M.D., F.A.C.P.: It very much gets at the question of whether you have early-stage or advanced breast cancer. In early-stage breast cancer, we tend to be very dogmatic about sticking with regimens that have been studied extensively in clinical trials, are FDA approved (with the exception of Herceptin which is not yet, but soon to be approved) and whose toxicity we understand.
So no one would use the results of the phase III trial with Abraxane to use Abraxane in early-stage breast cancer. There, the role is for Taxol or Taxotere. Abraxane is otherwise known as nanoparticle Taxol, or albumin-bound Taxol, and it was shown in clinical trials to be somewhat better than Taxol and to avoid some of the toxicities of Taxol. It is FDA-approved for breast cancer. Again, it is up to the physician and patient when Abraxane is used and whether it's used instead of Taxol in metastatic breast cancer, but it is not a drug that has data for early stage disease. A Phase III clinical trial is a study that is being done in a specific population of cancer patients where a standard treatment is compared to a newer treatment that has shown promise in that area, i.e. comparing Abraxane to Taxol. -
Hi FloridaLady,
I was in a small Stage I clinical trial evaluating the cardiac safety of giving Avastin concurrently with chemo (AC, Abraxane). It hasn't reported results yet as far as I know, but even when it does, unfortunately it won't have any answers to the question of whether Abraxane or Taxol are more effective.
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Florida Lady,
Abraxane does not stop mets, it "treats them" I think this is the key to this chemo.. Best response seems to be in the lung and liver. If you do not have these kinds of mets it doesn't really help you.
I just read your post and I am very upset since I am on Abraxane, had my 6th treatment this Monday and I don't have lung or liver mets. Latest scans and biopsy showed L4 lumbar spine so this is what onc change to. I have lost my hair all over after 2nd treatment and this is a harsh chemo for me. I have been on worse 3 years ago. I asked onc is this working and she will be doing scans again. I am really confused. How did you find out it doesn't really help if you don't lung and liver mets?
Take care,
Geech
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Geech,
Sorry you having such a hard time. I read this somewhere last year...but also when I have talk to doctor's at the three different clinic's I have been too over the last three years...they said "this chemo was tested on this kind of mast. disease with good results, but not tested for other mets as of now." Also I have talked to many ladies who was put on this chemo with these areas as mets only. Could you be in a trial and not know it? See the post above by from a quote at this website. They have been using this in trials. Ask your doctor why he chose this drug and what information he used to make his decision. He may have some cutting edge info we don't know about yet. Have you spoke to other with bone mets on Abraxene? I do believe it is used for bone mets also for the past few years. It's kind of the first drug when you get with mets they seem to use and than move off from there. Like everyone using Adrain. first and change off after that. I don't stay up on bone mets because TN ladies rarely have these kinds of mets.
Ask your doctor your list of questions. Also you can research online how Abaxene works with bone mets. I do believe it is the first line of treatment. I hope it works wonderfully for you.
Flalady
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Geech, one of my chemo buddies has been fighting IBC for 8 years now. Last fall she had a recurrence & was put on Abraxane ~ she has had a complete response to it, woohoo! Hopefully you are just as successful with your tx!
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Vicki,
What were your friend mets? I know a couple of ladies and very good lung & liver response. Was your friend bone?
Flalady
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Actually she does not have mets, just recurring IBC. She is not TN tho, so not sure if that has made a difference.
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Oh am I ever happy to find this thread...and Hi again Fla Lady! I am on Abraxane for early stage. I am on a 3 week on, 1 week off (X 4) of Abrax, Carboplatin and Herceptin. Most of you probably know that being HER+ requires Herceptin for a year so after chemo, I'll have that once every 3 until next Jan. It wasn't originally planned that way but I had a nasty post op infection after my double mast. and almost lost the expanders. Here's what my Onco's thinking is after he had me on almost 2 weeks of daily IV Vancomyacin to clear the infection (I fired my PS when he saw me, took more saline out of the expanders and sent me home with NO ABX!). He changed the orig. 3 wk protocol because he felt my risk from reinfection was less with a smaller dose weekly. He is heavily involved in the cancer research area at the local univ teaching hosp. and felt that the Abrax might cause less se's including further aggravating my bi-lat. carpal tunnel. He did have to fight insurance for it because it is $$$$$. Thank God, I have good insurance and because I HAVE to work during chemo and do a lot of computer work, I think that may have tipped the scales in my favor. Though there can be neuropathy issues on this (I do have some tingling), he felt it may be less so then the steroids. So far, I have the normal se's that all have expressed though the fatigue may not be as bad as A/C. Haven't lost a hair yet but I have made a wig appt. for the weekend because it's a pretty good bet I will (he did say some of his patients hadn't) My biggest issues are digestive, I don't know if it's that particular drug, or the carbo but my stomach is in havoc hell.I had read somewhere on this site about using the sea bands used for motion sickness to aid in nausea. They fit on your wrists with a button like thingy placed between 2 tendons in the wrists. I do believe they have helped me a ton. Don't wear them to bed though! At least for me, the next AM, my hands looked like cute little balloons. Too bad they don't make bands for your butt though! I've know every tile in my bathroom intimately now.
Anyway, I was so glad to see this thread as I have yet to see any posts by early stagers on either Abraxane or on the same schedule as me. And I am definitely not part of a clinical trial.I sure hope this works because I just cannot see myself doing this again. I just posted on another thread that I think I'd max out my credit cards, see every place I've ever wanted to see and enjoy my then short lived life. I know I could change my mind on that but that's how I feel today!
Bless you all
Ellen
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Ellen,
You sure have had a time with all this. I hope Abrax kicks but for you. I tried the sea bands on a cruise once and felt they helped me also. Try and get your hands/feet massaged by someone who can do a deep massage. This will really help with the neuropathy. Also get arch supports for your feet before you start having problems. They also help a lot.
Best to you
Flalady
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