Capecitabine

I was on Capecitabine for 5 months; just swapped over to Trodelvy as I have TNBC which has spread to bones.  I found Capecitabine slightly better side effects than previous IV chemo 4.5 years ago.  I initially had dry mouth but that went away; a bit of fatigue, but nothing like previous chemo. Worst side effect is what has already been highlighted- hand/foot syndrome. My feet got really hot, felt tender to walk on, tried lots of different creams. I found Dermal Therapy with urea the most soothing.  Only thing that really fixed the side effect of blistering/ peeling feet was to lower dose.  I started at 3250 mg / day and end up at 2200mg which seemed tolerable.   It did help reduce my tumour markers, but I have now swapped to new chemo more targeted for TNBC….. but harsher side effects 😰