I think it’s become a very interesting time in CML. It’s been 30 years since Brian Druker published the in vitro data on imatinib, 25 years since we have imatinib approved. And after a lot of progress there and then with second generation, it looked like we were done. And little by little, we started realizing there’s many more challenges. And now we have a series of new drugs, bosutinib recently, and many others that are being developed that look very exciting...
I think it’s become a very interesting time in CML. It’s been 30 years since Brian Druker published the in vitro data on imatinib, 25 years since we have imatinib approved. And after a lot of progress there and then with second generation, it looked like we were done. And little by little, we started realizing there’s many more challenges. And now we have a series of new drugs, bosutinib recently, and many others that are being developed that look very exciting. And that is because we still have a lot of issues that we need to overcome. Only a fraction of patients can stop therapy effectively. The patients who continue therapy, they have a lot of these low-grade toxicities, quality of life, tolerability issues. We still have questions about, for example, the subset of patients that have ASXL1 mutations. So there’s a lot of questions that we’re still trying to answer. It’s good that we have a resurgence of research trying to address these questions, and we’re going to be talking about some of those questions and upcoming possible solutions for that.
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