AC-PACLitaxel (dose dense) Treatement

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Cal05
Cal05 Member Posts: 3

I've just completed 4 doses of AC chemo and had my 1st of 4 doses of Paclitaxel (Taxol) yesterday. I'm going every two weeks. My chemo infusion for Taxol was 3.5-4hrs. I'm wondering if anyone has iced their hands and feet for this length of time? I know a few BC survivors who've had Taxol and have iced but their Taxol treatments were for 1hr-1hr15min. I iced with gel packs yesterday for the whole duration...it was long. Today I'm not sure if my fingers are sensitive from the icing or the Taxol!! Just curious if anyone else has or is doing this. I know there are no clinical proven studies but I'm trying to prevent neuropathy at all costs. Any input from those doing 3.5-4 Taxol treatment would be great. Thanks

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  • Denise-G
    Denise-G Member Posts: 1,777
    edited August 2016

    Oh gosh, I am an advocate for icing hands and feet, but for one (1) hour Taxol infusions (you ice only when Taxol is being infused - not other preparatory drugs). Your 3.5 to 4 hour infusion is a long time. It doesn't sound healthy to me to ice for that long! You don't want to get frost bite on top of everything else! I wish I had more helpful advice.


  • Maya15
    Maya15 Member Posts: 323
    edited August 2016

    Hi Cal05,

    I did it. It certainly was torture but I figured since neuropathy is permanent, I was going to suffer through 12 hours of icing (total) to prevent it, rather than face a lifetime of misery. My MO said it's even more important for dose dense because neuropathy is much more likely and more severe. She now advises all her patients to do it.

    I have 2 recommendations: get your icing set up right and find a way to distract yourself to pass the time. My infusions were 3 hours (just the Taxol, then I had Herceptin and Perjeta on top). The nurses set up the ice for me: plastic tub with a bag of ice cubes under feet and one on top, then another similar tub for the hands. I refused the gel packs because they only last 15 mins and they're not that cold. They changed the ice once during the infusion. When it got too cold I took hands and feet out briefly then put them back in.

    For passing the time, my hospital has wifi, so I picked a Netflix series and watched it. Couldn't read because I didn't want to keep taking hands out of the ice to turn the pages. I bought a bag of my favorite chocolate and rewarded myself with one every 20 mins during the infusion. I am really glad I did it. Two of my friends have crippling neuropathy from chemo.

  • Cal05
    Cal05 Member Posts: 3
    edited August 2016

    Thank you everyone for your replies. I appreciate it.

    Maya15 - So happy to hear someone else has done this over the 3hr course. Even HAPPIER that it worked for you!! I've heard so many great results from those having success through the 1hr infusion however I hadn't connected with anyone who had done the 3hr infusion. Did you have any trouble with frostbite? Or did you manage well enough to just keeping taking your hands/feet in/out to warm them up a bit? Myself, having only used the ice packs last Monday, you're right I had to change them 5-6 times because they thawed pretty quickly. This time I will arm myself with Ziplock bags and basins. I was just concerned about other issues that might arise due to having your hands in ice for 3 hours. However, I'm just really happy to know it worked for you, I'm willing to go all in too. I'm assuming you wore little sockets and thin gloves?

  • Maya15
    Maya15 Member Posts: 323
    edited August 2016

    I wore socks. Didn't wear gloves but my cancer center provided a towel to put between the ice bags and the hands. I had no problems with frostbite. All you need to do is lift hands and feet up for a few seconds when it feels too cold, then put them back again.

    It's worth phoning up your chemo center to see what they can provide. Ice is commonly used so they might have a freezer, ice cube machine, basins, ziplock bags, towels etc, and that saves you having to bring your own stuff. For me they provided everything.

    To Marie, as I understand it for Taxol there are 2 main protocols, 12 weekly infusions or 4 dose dense. They're both equally effective, but dose dense has a lot more side effects. I've done both. My blood counts dropped on the weekly and I couldn't handle going to the hospital 3 times a week for shots, so they switched me to dose dense with neulasta.

  • Cal05
    Cal05 Member Posts: 3
    edited August 2016

    Maya15 - Thank you for your reply. Sorry for the delay in posting. My last Round took me a little longer to bounce back. I'm surprised there are no others posting their results here.

    I'm going to follow your advice. I will post again when I've completed all my treatments. Fingers crossed my results after icing will be like yours.

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