oesophageal cancer life expectancy with no treatment

my step grandad has just been diagnosed with terminal oesophageal cancer.  He is 92 and they are not offering him any treatment other than a stent to be put in so he can try and eat.  He stopped being able to eat solid food and had a biopsy, within the 2 weeks it took to get the results he has struggled now to manage to eat the soup and liquidised food he has been having.  

They have offered to put a stent in on Christams eve but he has declined as he doesn't want to be in hospital for Christmas. So they are going to do it after Christmas (not sure of the date).

What i wanted to know is if anyone has any idea of how long we can expect him to live for.  My dad died of the same cancer nearly 10 years ago and he had a year from diagnosis but he had chemo which gave him extra time.

I am convinced that he won't have a lot of time but I just wanted to get a rough idea in my head if we are looking at weeks or months.

Parents
  • My dad diagnosed stage 4 oesophagus cancer in May. We was told without treatment 4 months. He started chemo but didn't really agree with him. Had a stent put in in September and October another 2 rounds of chemo but again stopped because he was to weak. Now we are nearing the end. Such a horrible disease 

    prayers your way

Reply
  • My dad diagnosed stage 4 oesophagus cancer in May. We was told without treatment 4 months. He started chemo but didn't really agree with him. Had a stent put in in September and October another 2 rounds of chemo but again stopped because he was to weak. Now we are nearing the end. Such a horrible disease 

    prayers your way

Children
  • Hi there, 

    I've just come across your post whilst sitting with my mum who has end stage oesophagus cancer with secondary liver cancer. 

    She was diagnosed in June this year after being unable to eat and swallow properly.  When they discovered the problem it was already stage 4. Chemo was offered but my mum declined as she was already very weak with being unable to eat.

    She had a atent put in in September this year and it helped massively. She was able to keep a cup of tea down and eat very soft foods. We were told that without this she would eventually need suction to remove her silvia. 

    Now the secondary cancer has taken a hold and she has juandice and confusion. She's able to shuffle to the bathroom with help and knows who we are but a lot of the time she's sleeping.  She's taking in about 6 mouthfuls of food a day and maybe one full cup of tea. She has lost all emotion to her face and her speech is slurred.

    My dad and I are nursing her and we have the district nurses coming in daily to change the syringe driver. Our link to the hospice has been amazing and she comes weekly and has arranged things like a wheelchair and even a short stay last month in the hospice. She's now in the process of arranging Marie curie to come in 4 nights a week and carers for the other 3. My dad is deaf and I stay over as much as I can but we are scared she will get up and fall.

    There's no happy outcome from this cruel illness... We have just done our best to make her comfortable. We've put up her Christmas tree as she loves this time of year and she can lay on the sofa and enjoy the lights. 

    Blessings to your family xx