Checkpoint inhibitors and acute myelogenous leukemia: promises and challenges

被引:26
作者
Alfayez, Mansour [1 ]
Borthakur, Gautam [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, 1400 Holcombe Blvd,Unit FC4-2006, Houston, TX 77030 USA
关键词
Checkpoint inhibitors; immunotherapy; AML; PD-1; CTLA-4; TIM-3; nivolumab; ipilimumab; ACUTE MYELOID-LEUKEMIA; REGULATORY T-CELLS; CANCER-TESTIS ANTIGEN; ACUTE MYELOBLASTIC-LEUKEMIA; ANTITUMOR IMMUNE-RESPONSES; MINIMAL RESIDUAL DISEASE; 1ST COMPLETE REMISSION; VERSUS-HOST-DISEASE; DEATH LIGAND 1; INDOLEAMINE 2,3-DIOXYGENASE;
D O I
10.1080/17474086.2018.1459184
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Immunity, for treatment of acute myelogenous leukemia (AML), has been leveraged historically in the form of allogeneic stem cell transplantation. Checkpoint inhibitors (CPI) as positive modulators of immune response have been recent major breakthroughs in solid tumors.Areas covered: Emerging concepts and clinical data with CPIs in acute Myeloid Leukemia - the focus of this review- will be discussed. CPIs can potentially be effective in absence of actionable' mutations and are expected to be effective against poor-risk AML. Immune inhibitory checkpoint molecules are upregulated in both de novo and relapsed AML. Similar data also suggest role of checkpoint molecules in mediating resistance particularly to hypomethylating agent (HMA) therapy, which can potentially be reversed by using checkpoint inhibitors.Expert commentary: Ongoing clinical trials in combination with HMAs are showing early promise, with doubling of response than that seen in historic controls. The optimal combinations of CPIs and the optimal space that they will fit in the continuum of AML therapies need lot of in depth work.
引用
收藏
页码:373 / 389
页数:17
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