Stage 4 adenocarcinoma

  • 6 replies
  • 157 subscribers
  • 323 views

I've joined this group to support my husband who has recently been diagnosed with lung cancer. It's an adenocarcinoma with no mutations noted. It's stage 4 as in his r lung and metastases to chest lymph nodes and left adrenal gland.  He's been offered carboplatin and permetrexed as chemotherapy.  Just wanted to ask if anyone has any experience of this chemotherapy?  He can't have immunotherapy due to COPD and RA. 

  • Hallo Jules

    I had this permutation of chemotherapy awaiting an operation on my right adrenal gland. They couldn’t operate so I had SABRE instead (very targeted radio therapy). This was a secondary from adenocarcenoma.

    Anyway, the chemo was not nearly as bad as I expected. The cancer centre gives you anti nausea drugs and steroids to overcome any side effects. I had few side effects and although I only had two treatments it was manageable. They are very careful about the dosage as each session is carefully planned just to suit you. At the time they give the chemo, they monitor you carefully and looked after you very well. At our centre they also give you details of a dedicated line that will deal with any emergencies, day or night. They give you a large information sheet about all the possible side effects but pointed out you don’t have all of them. It’s rather individual

    I have COPD as well so no worries there at all.

    From what I understand everything is very carefully planned and dosage monitored. For support my husband was just around and helped when I needed it, doing the odd bit of shopping. I rested when I was tired and tried to eat healthily. Fruity tastes were very good as I had a weird taste in my mouth.

    I hope this info is useful but do ask specific questions as well.

    Best wishes DaisyBouquet

  • Hi Daisy

    I really appreciate your message. Thankyou for taking the time to reply. My husband is not dealing too well with his diagnosis so I'm hoping once he starts the chemo he will feel more in control. Wishing you well on your treatment journey x

  • Hi Jules, 

    As you know it’s difficult to get your head round. It’s all the waiting and for your husband, perhaps the fear of chemotherapy. There has been so much said about how awful everything can be. It’s not always easy but I agree with you. Maybe it will be easier once your husband has started his chemo. When is it due to start? Keep your chin up.

    Love Daisy xx

  • Hi Daisy

    Yes I think you are right. Hes probably heard or read about all the side effects and horror stories. I'm hoping to allay some of his fears and get him to ask lots of questions so that hopefully he's more reassured. He's due to start on the 9th Feb so fingers crossed its better than we think.

    Thanks again x

  • Hello Jules, I’m 62 and had Adenocarcinoma. I had 4 sessions of Chemo with same meds you mentioned, but with several others to help with the therapy. After chemo they removed half my right lung, I’m still recovering but doing well.

    as far as the chemo, I found that the more protein I had, the better I handled the therapy.. protein shakes, eggs, meat,,,  protein was my answer. I hope this helps,

    Mark

  • Thankyou so much for your reply. I will try and make sure John keeps on top of his protein intake. Good luck on your journey x