Gemtuzumab ozogamicin and novel antibody-drug conjugates in clinical trials for acute myeloid leukemia

被引:37
|
作者
Yu, Bo [1 ]
Liu, Delong [2 ,3 ,4 ]
机构
[1] Lincoln Med Ctr, Dept Med, Bronx, NY USA
[2] New York Med Coll, Dept Med, Valhalla, NY 10595 USA
[3] Westchester Med Ctr, Valhalla, NY 10595 USA
[4] Zhengzhou Univ, Dept Oncol, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China
关键词
Gemtuzumab ozogamicin; Antibody-drug conjugate; CD33; CD123; CLL1; RECEPTOR-ALPHA CHAIN; I TREAT; OLDER PATIENTS; INDUCTION CHEMOTHERAPY; SALVAGE THERAPY; AML PATIENTS; INTENSIVE CHEMOTHERAPY; TARGETED CHEMOTHERAPY; MYELOGENOUS LEUKEMIA; DOSE CYTARABINE;
D O I
10.1186/s40364-019-0175-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeted agents are increasingly used for the therapy of acute myeloid leukemia (AML). Gemtuzumab ozogamicin (GO) is the first antibody-drug conjugate (ADC) approved for induction therapy of AML. When used in fractionated doses, GO combined with the conventional cytarabine/anthracycline-based induction chemotherapy significantly improves the outcome of previously untreated AML patients. Single-agent GO is effective and safe for AML patient ineligible for intensive chemotherapy. Multiple combination regimens incorporating GO have also been recommended as potential alternative options. In addition, several novel ADCs targeting CD33, CD123 and CLL-1 are currently undergoing preclinical or early clinical investigations. In this review, we summarized the efficacy and limitations of GO as well as novel ADCs for adult AML patients.
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收藏
页数:13
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