Gemtuzumab ozogamicin for acute myeloid leukemia.

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

Blood

journal_title

Blood

authors

Appelbaum FR,Bernstein ID

doi

10.1182/blood-2017-09-797712

subject

Has Abstract

pub_date

2017-11-30 00:00:00

pages

2373-2376

issue

22

eissn

0006-4971

issn

1528-0020

pii

blood-2017-09-797712

journal_volume

130

pub_type

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