Abstract:
:On 1 September 2017, the US Food and Drug Administration (FDA) approved gemtuzumab ozogamicin (GO) for the treatment of adults with newly diagnosed CD33+ acute myeloid leukemia and for patients aged ≥2 years with CD33+ acute myeloid leukemia who have experienced a relapse or who have not responded to initial treatment. This signals a new chapter in the long and unusual story of GO, which was the first antibody-drug conjugate approved for human use by the FDA.
journal_name
Bloodjournal_title
Bloodauthors
Appelbaum FR,Bernstein IDdoi
10.1182/blood-2017-09-797712subject
Has Abstractpub_date
2017-11-30 00:00:00pages
2373-2376issue
22eissn
0006-4971issn
1528-0020pii
blood-2017-09-797712journal_volume
130pub_type
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