You are welcome. I would add the non covalent binding btk inhibitors like GDC-0853 to the equation as well. I don’t know if technically they would be considered second generation ibrutinib drugs or not.
But as it relates to your question that seems to be exploring possible options, I think a non covalent binding btk inhibitor is very different than a btk inhibitor that binds covalently like Ibrutinib. It binds differently and might work for someone who has failed ibrutinib. I assume people who fail ibrutinib cannot expect true second generation btk inhibitors like acalabrutinib will work where ibrutinib failed, while a non covalent might work, that’s why I think of it as a different class of drugs.
Hopefully they are looking for ways to end run resistance if drugs like venetoclax and duvelisib fail too. It seems for many of us fighting Cll the game is cobbling together these drugs and hope the science of developing new drugs stays a step ahead of our Cll.
Thanks. I suggest that you consider saying that “the drug failed the patient,” thus, not unwittingly making the person feel ashamed or somehow responsible for the drug’s failure to work with the patient. My daughter, for example, felt that she had failed when, in fact, the multiple chemos had failed her. Not what she needed after 75 weeks of chemo and three years of fighting a cancer that is very rarely cured. Thanks.
First of all, I am so very sorry that your daughter had to endure such a difficult therapy for so long a time. That must have been very hard for you and her and her family and friends. Cancer is a horrible disease and everyone on here, in addition to their own cancer, probably has a person close to them fighting cancer.
I do get the distinction of saying a drug failed someone, not someone failed a drug. I will try in the future to say it’s the drug failing the person instead of the person failing the drug, even though they mean the same thing to me. I had a very difficult bout with hemolytic anemia and I failed treatments for it. It would not have helped me personally to have someone tell me the drug failed, not me, it didn’t occur to me I should be ashamed for not responding to a treatment.
I do not think most of the community on here is as sensitive to the distinction you raise. Are you a Cll patient? Just curious, with all the great info on the site it’s odd your first post would be to dig up a five month old post to suggest I was making people feel ashamed with my postings. I do try hard to give people helpful and considerate information. I do my best with the political correctness stuff, I have my own challenges with cancer and don’t parse every word I write and hope I am not offending people.
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