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Optimizing the role of brentuximab vedotin in classical Hodgkin lymphoma therapy

The US Food and Drug Administration approval of brentuximab vedotin (BV) in 2011 marked an important milestone in the management of classical Hodgkin lymphoma (HL). Although initially approved for use in the relapsed or refractory setting, its high efficacy and favorable toxicity profile led to nume...

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Foilsithe in:Hematology Am Soc Hematol Educ Program
Príomhúdar: Moskowitz, Alison J.
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Society of Hematology 2018
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6246031/
https://ncbi.nlm.nih.gov/pubmed/30504312
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