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The 48th EBMT Annual Meeting was held virtually on March 19-23, 2022. This meeting brought together healthcare professionals from all over the world to discuss the latest research in hematological transplantation and cellular therapies.
🎥 This #WorldLeukemiaDay watch @zucenka (@VU_LT) discuss data from a study investigating venetoclax combinations in FLT3- and IDH1-mutated acute myeloid #Leukemia:
As it's #WorldLeukemiaDay, why not listen to our recent podcast episode on the sequencing of BTKi therapy in CLL, which focuses on treatment considerations and emerging strategies.🩸
Click here to check it out:
🎧 https://ow.ly/8J5y50ZAsJV
🚨 The FDA approves ropeginterferon alfa-2b for the treatment of essential thrombocythemia!
This approval introduces the first new FDA-approved treatment for ET in nearly 3 decades, offering a long-acting interferon-based approach supported by durable response and hematologic
🧬 AAV gene therapy in hemophilia: what comes next?
Hear @RKaczmarekDr discuss the challenges of current AAV-based approaches, including durability, liver toxicity, and potential malignancy risks, alongside emerging non-AAV strategies.
The 48th EBMT Annual Meeting was held virtually on March 19-23, 2022. This meeting brought together healthcare professionals from all over the world to discuss the latest research in hematological transplantation and cellular therapies.
🎥 This #WorldLeukemiaDay watch @zucenka (@VU_LT) discuss data from a study investigating venetoclax combinations in FLT3- and IDH1-mutated acute myeloid #Leukemia:
As it's #WorldLeukemiaDay, why not listen to our recent podcast episode on the sequencing of BTKi therapy in CLL, which focuses on treatment considerations and emerging strategies.🩸
Click here to check it out:
🎧 https://ow.ly/8J5y50ZAsJV
🚨 The FDA approves ropeginterferon alfa-2b for the treatment of essential thrombocythemia!
This approval introduces the first new FDA-approved treatment for ET in nearly 3 decades, offering a long-acting interferon-based approach supported by durable response and hematologic
🧬 AAV gene therapy in hemophilia: what comes next?
Hear @RKaczmarekDr discuss the challenges of current AAV-based approaches, including durability, liver toxicity, and potential malignancy risks, alongside emerging non-AAV strategies.
Explore the latest updates in hematological stem cell transplantation, including expert interviews from major international congresses, podcasts and e-learning.
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