Enhertu treatment and quality of life
Can anyone who has gone through this tell me how the protocol for this treatment contributes to quality of life. As I understand it, one must continue the treatment until they can't take it anymore (they die, the treatment is unendurable)? There are other treatment available, which seem to display similar OS, such as LenPem, which does have an end point.
Any comments would be really welcome. I've got to decide what to do, given the two choices.
Thanks:)
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Hi … thank you. My fatigue is of the debilitating type. I can barely get out of bed and I have neuropathy in my legs due to the last treatment. I’ve had to hire a dog walker, really for the last year. Since the first dose of ENHERTU 8 days ago, I go in and out of sleep sort of like narcolepsy all day long. I am not able to do any activities except walk a short distance to my kitchen to get food that I’ve had delivered. Prior to this first dose I did not feel all that bad. In fact I went out to eat twice with my brother and went to a cookout at my cousin’s all within a span of a few days. Then I had the dose and wham I turned into a sick weak debilitated person I do not recognize or know.
Have you spoken with your oncologist? She/he may have to reduce the dose you're getting. I wouldn't wait to contact her/him. Really.
I took the advice of this group and consulted my oncologist on how sick I am on ENHERTU. He wants to try a dose reduction next time. Has anyone found this to be helpful? Thank you.
It should be helpful, although I'm taking the full dose. I'm glad you talked to your oncologist!