Literature DB >> 28756350

Immunotherapy in adult acute leukemia.

Sabine Blum1, Filipe Martins2, Michael Lübbert3.   

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.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Acute lymphoblastic leukemia; Acute myeloid leukemia; Antibody-drug conjugates; BiTEs; Blinatumomab; CART cells; Checkpoint inhibitors; Immunotherapy; Inotuzumab

Mesh:

Substances:

Year:  2017        PMID: 28756350     DOI: 10.1016/j.leukres.2017.06.011

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  5 in total

1.  CD38 as a therapeutic target for adult acute myeloid leukemia and T-cell acute lymphoblastic leukemia.

Authors:  Jyoti Naik; Maria Themeli; Regina de Jong-Korlaar; Ruud W J Ruiter; Pino J Poddighe; Huipin Yuan; Joost D de Bruijn; Gert J Ossenkoppele; Sonja Zweegman; Linda Smit; Tuna Mutis; Anton C M Martens; Niels W C J van de Donk; Richard W J Groen
Journal:  Haematologica       Date:  2018-09-06       Impact factor: 9.941

Review 2.  Chimeric antigen receptor T cell targeting B cell maturation antigen immunotherapy is promising for multiple myeloma.

Authors:  Tiantian Ma; Jing Shi; Huasheng Liu
Journal:  Ann Hematol       Date:  2019-01-28       Impact factor: 3.673

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

Authors:  Yong Li; Gang Deng; Huikai Zhang; Yangzhi Qi; Lun Gao; Yinqiu Tan; Ping Hu; Yixuan Wang; Baohui Liu; Qianxue Chen
Journal:  Aging (Albany NY)       Date:  2020-11-07       Impact factor: 5.682

4.  CCR2 signaling in breast carcinoma cells promotes tumor growth and invasion by promoting CCL2 and suppressing CD154 effects on the angiogenic and immune microenvironments.

Authors:  Gage Brummer; Wei Fang; Curtis Smart; Brandon Zinda; Nadia Alissa; Cory Berkland; David Miller; Nikki Cheng
Journal:  Oncogene       Date:  2019-12-11       Impact factor: 9.867

5.  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.

Authors:  Xudong Yang; Jisheng Liu
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  5 in total

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