[cParticipant]

Thanks for getting back to me. Unfortunately for some reason it hasn’t been approved in Scotland. So disheartening as I am desperate for him to still have a treatment available to him.

[cParticipant]

Thank you for getting back to me regarding the treatment. I hope you both continue to do well & it pushes the myeloma back.
I feel so disheartened that the advice we were given for my loved one was to stop the Elranatamab. During the first 7 weeks, his paraprotein did increase twice, after 2 bloods were taken during the first 4 weeks & then after week 6 or 7. And from those they have decided that he is not responding to the treatment. I am gutted & feel a sense of despair. I have heard of others taking some time to respond & like you said they took your bloods after 10 weeks. I just feel it is too soon to stop but I am not a Haematologist. I was hoping to read that for some people Elranatamab became effective after 8 weeks – just to give me hope. There are no more treatments left for him & it is utterly devastating.

[cParticipant]

Hi there,

Just wondering if anyone has been on Elranatamab? I am looking for some hope. A loved one has only had 8 weeks of this treatment because his myeloma relapsed & his paraprotein started to increase. Since only 7 weeks have gone by his most recent paraprotein levels have increased slightly more. Does this mean the treatment isn’t working & he should stop or should we give it another month?

[Author]

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