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Blood Podcast
Blood Podcast

Season 1, Episode 17

18 min•23 april 2020

Om avsnittet

This week’s episode will highlight the development of a factor VIII replacement therapy for patients with severe Hemophilia A, examine a novel pathway of resistance of FLT3-ITD+ AML cells to FLIT3 inhibitors, and review long-term results of a pilot study in children with low risk B-cell ALL conducted in a limited-resource setting.

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Designing Durable Remissions in Relapsed AML and Follicular Lymphoma

16 min

Dose Makes the Cure: Venetoclax in Ph- ALL

14 min

Exploiting Vulnerabilities in High‑Risk MM and Mapping the Red Cell Interactome

30 min

MYB driven ALL and Venetoclax-Azacitidine damage to Bone Marrow

25 min

Predictive Markers of Glofitamab Resistance in R/R B-NHL

16 min

Better Together: Adding daratumumab for AL Amyloidosis and and Mezigdomide for MM

26 min

Balancing Infection and Thrombosis: Bispecific Antibodies and the Many Roles of HRG

15 min

Cost-Effectiveness of Current SCD Treatments and Potential Therapeutic Targets for Fetal Hemoglobinopathies

33 min

HLH-like toxicities after CAR-T and Structure-Function Relationships of FNAIT

17 min

FLT3-ITD microclones in AML and Results from the RESET-PV trial

14 min

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