Hi Trivia,I think your reply was related to what I posted (not Colleen) so I’ll respond as if that’s true. My first Mets location was my stomach and 16 months later discovered liver lesions. I started Ibrance at that time and had two CT’s in 5 months where we thought the disease was stable until the MRI already mentioned. I am taking Zeloda, a pill form of chemo instead of traditional chemo which the oncologists thought I’d be able to tolerate better given weight concerns. I’m only on the second cycle (two weeks on, one week off) and side effects to date have included face rash, mouth sores and hand/foot syndrome; certainly not pleasant but I’m managing. Will do another scan after four cycles to see if helping. It can be really daunting to read/absorb/process drug statistics, for me it helps to reference websites such as this one to get insights to what others have experienced, and keeping the faith that I’ll be one of those women to live for lots and lots of years with a Mets diagnosis. Wishing you well, Trivia, as you move along the Mets journey.