» Articles » PMID: 28756350

Immunotherapy in Adult Acute Leukemia

Overview
Journal Leuk Res
Date 2017 Jul 31
PMID 28756350
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The treatment of acute myeloid leukemia (AML) did not evolve profoundly in the last decades. Some improvement has been made for acute lymphoblastic leukemia (ALL). Emerging new treatment modalities, such as immunotherapy, are now beginning to be available for acute leukemia, mostly for patients suffering from ALL. This review aims to give an overview of these new therapeutic approaches, especially those already available. The focus is on cell-based immunotherapy, or molecules using preexisting host cells. Underlying mechanisms are explained and an overview of clinical experience with phase 1-3 studies is given. Immunotherapies discussed are antibody-drug conjugates, bispecific T-cell engagers (BiTEs), chimeric antigen receptor T cells (CARTs) and immune checkpoint inhibitors (ICPIs). Most of the clinical studies reviewed are in ALL patients, usually in the relapse setting, but where available, studies on AML patients were also considered. This new general treatment approach offers hope to patients with until now dismal clinical outcome. Hopes are high that future developments, and moving these therapies to an earlier treatment phase, will improve the prognosis of patients suffering from acute leukemia.

Citing Articles

CDKN1A is a target for phagocytosis-mediated cellular immunotherapy in acute leukemia.

Allouch A, Voisin L, Zhang Y, Raza S, Lecluse Y, Calvo J Nat Commun. 2022; 13(1):6739.

PMID: 36347876 PMC: 9643439. DOI: 10.1038/s41467-022-34548-3.


Targeting PD-L1 (Programmed death-ligand 1) and inhibiting the expression of IGF2BP2 (Insulin-like growth factor 2 mRNA-binding protein 2) affect the proliferation and apoptosis of hypopharyngeal carcinoma cells.

Yang X, Liu J Bioengineered. 2021; 12(1):7755-7764.

PMID: 34608837 PMC: 8806995. DOI: 10.1080/21655979.2021.1983278.


Weighted gene correlation network analysis identifies microenvironment-related genes signature as prognostic candidate for Grade II/III glioma.

Li Y, Deng G, Zhang H, Qi Y, Gao L, Tan Y Aging (Albany NY). 2020; 12(21):22122-22138.

PMID: 33186124 PMC: 7695422. DOI: 10.18632/aging.104075.


B7-Positive and B7-Negative Acute Myeloid Leukemias Display Distinct T Cell Maturation Profiles, Immune Checkpoint Receptor Expression, and European Leukemia Net Risk Profiles.

Antohe I, Dascalescu A, Danaila C, Titieanu A, Zlei M, Ivanov I Front Oncol. 2020; 10:264.

PMID: 32231996 PMC: 7082324. DOI: 10.3389/fonc.2020.00264.


Phase 1b/2 study of blinatumomab in Japanese adults with relapsed/refractory acute lymphoblastic leukemia.

Kiyoi H, Morris J, Oh I, Maeda Y, Minami H, Miyamoto T Cancer Sci. 2020; 111(4):1314-1323.

PMID: 31971321 PMC: 7156857. DOI: 10.1111/cas.14322.