Π£ Π½Π°Ρ Π²Ρ ΠΌΠΎΠΆΠ΅ΡΠ΅ ΠΏΠΎΡΠΌΠΎΡΡΠ΅ΡΡ Π±Π΅ΡΠΏΠ»Π°ΡΠ½ΠΎ Chronic Myeloid Leukemia: Diagnosis and Treatment ΠΈΠ»ΠΈ ΡΠΊΠ°ΡΠ°ΡΡ Π² ΠΌΠ°ΠΊΡΠΈΠΌΠ°Π»ΡΠ½ΠΎΠΌ Π΄ΠΎΡΡΡΠΏΠ½ΠΎΠΌ ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅, Π²ΠΈΠ΄Π΅ΠΎ ΠΊΠΎΡΠΎΡΠΎΠ΅ Π±ΡΠ»ΠΎ Π·Π°Π³ΡΡΠΆΠ΅Π½ΠΎ Π½Π° ΡΡΡΠ±. ΠΠ»Ρ Π·Π°Π³ΡΡΠ·ΠΊΠΈ Π²ΡΠ±Π΅ΡΠΈΡΠ΅ Π²Π°ΡΠΈΠ°Π½Ρ ΠΈΠ· ΡΠΎΡΠΌΡ Π½ΠΈΠΆΠ΅:
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Π‘ΠΏΠ°ΡΠΈΠ±ΠΎ Π·Π° ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ ΡΠ΅ΡΠ²ΠΈΡΠ° ClipSaver.ru
Michael Mauro, MD, Director of the Chronic Myeloid Leukemia Program at Memorial Sloan Kettering Cancer Center, discusses the diagnosis and treatment of chronic myeloid leukemia (CML). CML is a myeloproliferative neoplasm characterized by the expression of the BCR-ABL1 fusion gene. It presents with neutrophilic leukocytosis; 90% to 95% of patients have a shortened chromosome 22, also called the Philadelphia chromosome. The condition can manifest at any age but most commonly affects middle aged and older individuals. Patients usually present with fatigue, weight loss, anemia, night sweats, and splenomegaly. Approximately 50% of patients diagnosed with CML are asymptomatic and diagnosed due to routine complete blood count. Blood-based testing is most commonly used in diagnosis, however, a bone marrow test gives a better understanding of the biology of the disease. Genetic testing can also be useful in identifying genetic mutations in the Philadelphia chromosome. Allogeneic stem cell transplantation and tyrosine kinase inhibitors are traditional first-lines of therapy for this condition. There are currently four U.S. Food and Drug Administration (FDA) approved tyrosine kinase inhibitors for first-line therapies for patients with CML: imatinib, bosutinib, dasatinib, and nilotinib. There are also several other therapies approved, or in development, as second- and third-line therapies for this rare cancer. Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML) is a chronic condition requiring long-term treatment. Nilotinib has been a trusted treatment for over 17 years, primarily available as Tasigna capsules, which requires strict fasting, posing challenges to patientsβ routines and treatment adherence. In November 2024, the FDA approved Danziten, a new nilotinib tablet formulation that eliminates mealtime restrictions while maintaining efficacy and safety. Unlike Tasigna, Danziten can be taken with or without food and uses a re-engineered formulation to enhance bioavailability and reduce food-related risks, including QT prolongation. Danziten is now included in the National Comprehensive Cancer Network (NCCN) guidelines for CML, but it is not interchangeable with other nilotinib products due to differences in formulation and dosing.