Hi everyone.
I'm currently on docxirubicin which I've been having dose dense every 2 weeks along with zoldronic acid. I am changing over to paclitaxel for my next 4 cycles. I've been reading up on it and it mentions that the infusion time compared to the docxirubicin is much longer...as long as up to 4 hours.
Any one else can please share experience of this?
Thank you in advance x
Not in my experience. I had a form of paclitaxel in my first chemo, same infusion time as with the doxorubicin which was part of my second regimen.
A lot depends on patients' tolerance but also on the mix of drugs, so it is possible that two people on exactly the same chemo would experience different infusion times if tolerance is varied, and it is also possible that the variation would be the result of what else is being given.
Hi FE1
I had dose dense EC then paxitaxol every second week like youre having. Originally my paxitaxol was due to be given over 3.5 hours with time either side for flushing. I had a reaction when I had my second round of taxol so they increased the time to 5.5 hours and gave me twice the pre meds. I was so worried they'd reduce my dose that I didn't mind staying longer and the premeds were so strong I was in a weird buzzed daze for the whole day!
I hope you find out soon what you can expect from paxitaxol and good luck with the rest of your chemo
Cheers
Lizzy
If its every 2 weeks, then its a 3 hour infusion usually, but I found with the usual pre-infusion questions and 3 premeds, that the whole thing took 5 hours each time. The premeds include piriton which makes you really drowsy, so wouldn't recommend driving yourself home after this one. I hope it goes well for you.
Hi Lizzy. Thank you for your reply. Sorry to hear that you have had a reaction to paclitaxel. I know I've read a few posts saying the same thing. I'm praying mine goes ok and the time is about 3 hours. I have a picc line too so know that there's time either side for that too. Thank you again x
Hi Zephyr. Thank you for your reply. I guess I'm going to have to take more reading material in with me if it's so long. Think I've been lucky so far with the shorter treatments. How was the monitoring on paclitaxel. Do they take blood pressure more? Thank you
The only thing that occurred to me is that for triple negative cancer the paclitaxel is a weekly infusion over an hour or so. The monitoring was not any more, but they keep an eye on you in case you react to it a little - my face went bright red like a tomato on my last one! You will probably sleep your way through it but take reading material in case. I found it was ok - I wore ice gloves and socks that I bought from amazon to limit the neuropathy that you can get with it and also to limit nail damage. It helped a lot, though I must admit, my nails are still a little delicate now and need nail polish and filing not cutting, and I wear gloves for household chores. Overall though I found paclitaxel was OK.
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