newly diagnosed with met uterine to liver and lungs any advice using carboplatin and gemcitabine

Sorry to hear of your mets to your liver and lungs.  I have not had that combination.  I had 9 taxo/Carbo treatments and 10 taxol/ cisplatin treatments.  I wish you well with your treatments, and hope you do not have many side effects from it.  Sorry you have to join us on this. Journey.  In peace and caring.

fnpanda said:

Thank you

I am very grateful for your welcoming response.  I've been dealing with uterine cancer since 2005 with internal radiation and surgery the first time, second it came back on the pelvic wall and now has mets to liver and lungs.  I am very torn between doing chemo and the small chance it would do anything and living my remaining life without any treatment.  The chemo wiped out 2 years of my life and made me very sick.  I don't know how to find out how much time I may have left.  Current pet scan showed hot spot on uterine wall, cancer on the surface of the liver, 2 nodes in one lung and 1 in the other.  I just lost my best friend to lung cancer and she passed in 9 weeks but two of her final weeks she was unresponsive.

your cancer has progressed to this point.  I have not had a recurrence but often think about what I'll do if it happens.   I don't believe there is a right or wrong answer to your dilemma.  My chemo was the same as Ro's initial treatment.  I am not familiar with the second drug offered you but I'll be googling it (I'm a retired nurse so have a natural interest).  Are you confident in your medical team and their recommendations?  Do you feel you can talk frankly with them about your feelings?  How do your loved ones play into this?

Hopefully someone will show up soon with advice/dialog based on experience.  At any rate, please keep coming back.  We will try to help and, with all you've been through, you have much to offer us.  

take care

I'm so sorry to hear this news.  I am on treatment for my third recurrence.  First one was at vaginal vault - zapped with external radiotherapy and I was OK for 2.5 years.  Second recurrence on pelvic sidewall -  major debulking surgery followed by 6 cycles of carbo/taxol.  OK for 15 months.  Third recurrence on pelvic sidewall - no surgery due to location.  However this third recurrence is responding well to hormone therapy (aromatase inhibitor - letrozole) as my tumours are oestrogen receptive.  Perhaps hormone therapy might be an option for you to explore at this stage? My oncologist assures me that she has had ladies stay stable on hormone therapy for several years.  I do hope that it might be an option for you as it is a relatively easy treatment to tolerate and I have a good quality of life on it.
Kindest wishes
Helen

HellieC said:

Sorry to hear of your recurrence

I'm so sorry to hear this news.  I am on treatment for my third recurrence.  First one was at vaginal vault - zapped with external radiotherapy and I was OK for 2.5 years.  Second recurrence on pelvic sidewall -  major debulking surgery followed by 6 cycles of carbo/taxol.  OK for 15 months.  Third recurrence on pelvic sidewall - no surgery due to location.  However this third recurrence is responding well to hormone therapy (aromatase inhibitor - letrozole) as my tumours are oestrogen receptive.  Perhaps hormone therapy might be an option for you to explore at this stage? My oncologist assures me that she has had ladies stay stable on hormone therapy for several years.  I do hope that it might be an option for you as it is a relatively easy treatment to tolerate and I have a good quality of life on it.
Kindest wishes
Helen

Hi HellieC, Can I ask how you take Letrozole. Pills or Capsules or injections? Apparenlty pilss are non-steroidail inhibitor and capsules or injections are chemo agents. Thanks Pav