Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Apr;14(2):106-118.
doi: 10.1007/s11899-019-00503-1.

Recent Advances in Adult Acute Lymphoblastic Leukemia

Affiliations
Review

Recent Advances in Adult Acute Lymphoblastic Leukemia

Guillaume Richard-Carpentier et al. Curr Hematol Malig Rep. 2019 Apr.

Abstract

Purpose of review: This article reviews the recent advances in the pathophysiology and management of acute lymphoblastic leukemia (ALL) in adults.

Recent findings: Addition of rituximab to standard chemotherapy improves survival in the frontline treatment of B cell ALL, and measurable residual disease (MRD) is the most important prognostic factor. Tyrosine kinase inhibitors (TKI), particularly ponatinib, in combination with Hyper-CVAD significantly improve outcomes in Ph + ALL challenging the benefit of allogeneic stem cell transplant in first line for these patients. Blinatumomab, inotuzumab ozogamicin, and chimeric antigen receptor (CAR) T cells are better options than chemotherapy alone for the treatment of relapsed or refractory ALL. Combination of these agents with chemotherapy and their incorporation in the frontline setting show promises to improve cure rates of ALL. Development of monoclonal antibodies, CAR T, and potent TKI has improved the outcome of ALL. Advances in our understanding of ALL biology are expected to bring new therapeutic strategies in the upcoming years.

Keywords: Acute lymphoblastic leukemia; Chimeric antigen receptor T cells; Management; Monoclonal antibodies; Treatment.

PubMed Disclaimer

References

    1. Blood. 2012 Aug 30;120(9):1868-76 - PubMed
    1. Br J Haematol. 2016 Feb;172(3):439-51 - PubMed
    1. Lancet Oncol. 2015 Jan;16(1):57-66 - PubMed
    1. J Clin Oncol. 2017 Feb;35(4):394-401 - PubMed
    1. Blood. 2015 Aug 6;126(6):746-56 - PubMed

MeSH terms

LinkOut - more resources