Hi there
I'm new to the group
I was diagnosed in April with TNBC and have just finished my rounds of chemo and my Op is next month.
My question is has anyone been given, or going through immunotherapy treatment?
I believe it is administered like chemo and the course is a year.
I've never looked online other than official Macmillan or Cancer Research sites and today learned the side effects can be like that of chemo.
Does anyone have experience of this and are the side effects as bad?
I must say the treatment I have received on the NHS has been outstanding and I'm feeling very positive about my Op, but the thought of a year (14 months precisely) of a further treatment with potential chemo side effects makes me a little anxious.
I'm also slightly concerned that TNBC is more likely to come back?
Very grateful if anyone can share their experience or knowledge?
AA x
Hi Ali!
I begun chemo 5 weeks ago for TNBC but started Keytruda just a week ago along with the forth infusion. I have Paclitaxel & Carbo every week for 12 weeks plus Keytruda every 4th sessions. By the end of chemo I will have had 8 Keytruda plus another 9 Keytruda infusions(every month) after surgery.
I had a biopsy marker that indicated Keytruda may help: PD-1
If you need more information, google KEYNOTE 522
My regimen is doable with Keytruda adding back pain and a slight nausea. Manageable though... So I`m taking Nurofen and drink lots of ginger juice. I know there are other more serious side effects but I chose not to read about them...
I am concerned about possible recurrence too but I read many positive stories, also found out online that diets and supplements may fight recurrence after chemo ...and surely could add a sense of control. (I can send you few links but I am not sure is it allowed)
We will be ok XX
Shu
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