I’ve been diagnosed with stage 2A ovarian cancer. Had my surgery about 4 weeks ago. Starting Paxitaxel & Carboplatin this Wednesday. 6 sessions 3 weeks apart planned. I’d love to learn about your experience with this regimen in terms of quality of life and how you tolerated it. I had breast cancer 17 years ago and took 6 rounds of chemo back then. At the time it was a 3-drug combo called FAC. If anyone took both the FAC and paxi-carbo and cam compare , I’d appreciate even more. Thank you.
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Elifebru
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I had breast cancer 20 years ago and am now stage 4b OC, diagnosed 2 years ago and on Olaparib following carbo taxol. Don’t know what drugs I had for breast cancer but they worked! The breast cancer chemo was much harder than carbo taxol, for me. Lost allhair on both but am happy with wigs. Must have lost nearly a stone on breast chemo, lost none on OC chemo. I presume you have had a BRCA test. If not, you should ask for one. I am BRCA 2 but luckily my sons are free. With all good wishes, Emma x
thank you so much Emma. Much appreciated. I am BRCA 1&2 negative, but I am told there are additional genetic tests now which they will presumably do. I hope my carbo taxol goes smoothly, you gave me courage. Wishing all the best for you xx
Hi. Sorry you have to face a second cancer. Everyone is different in their experience of chemo. I found carbo taxol very difficult compared to the doxil and carbo I had for first recurrence. I was pretty much in bed for five or six days each cycle and had weakness and shortness of breath from anemia. I had a delayed reaction so I was fine until day 5 then overcome with nausea for the next six days. The last nine days of the cycle I was pretty normal though not vigorous. I took steroids and extra nausea meds for eleven days each cycle instead of the usual three. But that’s just my experience. You might breeze through it.
Hi Elifebru, I wasn’t offered surgery so know nothing of surgery related issues, I’m afraid. I’m stage 4OC and had pacli/carbo combo. First 3 days I thought, no side effects, this us wonderful! 😂 Then someone lobbed a brick at me (not literally, but that’s how it felt!). Terrible fatigue, couldn’t eat, really couldn’t function. If you live alone this is when you need help. After 5 days I started to feel better and then had nearly two weeks of ok life. Side effects I got are neuropathy in my feet, total hair loss (wig for me), droopy eye, food taste alteration and a few minor things I can’t remember (you move on). Initially they give you steroids to take home and I couldn’t sleep for two nights. If this happens tell your chemo nurses, they can help. This combo did a good job for me. Not totally because I’ve not had surgery but I’m jogging on. Very, very good luck and big hugs. Gill X
Gill thank you very much for sharing I really appreciate it. I feel like the 1st will be toughest as I don’t know what to expect. I can’t really compare to the chemo I took 17 years ago for a different cancer as it was different drugs. Wishing best for all of us and sending you love. Ebru
Hi - I was fine on taxol/carbo - total hair loss which wasn't a problem but no nausea, etc. Cooling cap gave me a terrible headache so took it off after 15 minutes. Steroids hyped me up for the three days after chemo but the chemo made me tired - odd feeling (a friend said her steroids forced her to clean her care at 7.00 am). Felt a bit sleepy so napped as necessary but generally led a normal life - if you can call lockdown normal. Good luck with this. x
Everyone is different as to how they react I'm in the states I chose to use the cooling cap I lost about 15% of my hair the cancer center that I got my treatments thru administered a pre- treatment side effect IV I took steroids for 3 days afterwards I never had any side effects except for being a bit wired but then tired after I came down from them I was fully functional I hope the same for you.
hoping smooth sailing also I bought those elf ear muffs that slide over each ear as it helped with the freezing my Hairdresser had BC survivors that used the cap she suggested I cut my hair short prior to treatment as it was easier for the cap to freeze follicles that was her experience.
this combo worked well for me in 2008. It kept me in remission for six years. Side effects were foot neuropathy, fatigue. My hair started thinning so I had it cut very short. Wore a wig or turbans. Wishing you the very best! 😘
thank you very much! Big help to read your experience which I understand was relatively good. Wishing you healthy months and many years. So glad you enjoyed the trip afterwards. Hope to plan for a nice Turkey trip (my homeland) in October after all is finished 💜 sending love🫶🏼
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