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Review
. 2017 Apr 19:4:32.
doi: 10.21037/sci.2017.03.04. eCollection 2017.

Immune checkpoint blockade for hematologic malignancies: a review

Affiliations
Review

Immune checkpoint blockade for hematologic malignancies: a review

Matthew J Pianko et al. Stem Cell Investig. .

Abstract

Immune checkpoint blockade has revolutionized the treatment of cancer, with impressive responses seen in a broad variety of tumor types. Blockade of immune checkpoints and immune signaling antibodies has shown promise in multiple types of hematologic malignancies (HMs), with dramatic single agent responses for pembrolizumab and nivolumab in Hodgkin lymphoma (HL). In this review, we outline the current state of immune checkpoint blockade drug development in HMs, and discuss mechanisms of activity and resistance, and highlight potential targets in the immune tumor microenvironment (TME). Blockade of T-cell checkpoint molecules PD-1/PD-L1 and CTLA-4 are the most clinically mature of the immune checkpoint strategies. Novel and upcoming strategies for immune checkpoint blockade drug development in HMs using innovative combinations to modulate immunologic targets shows significant promise as a way to expand the number of patients with blood cancers who could benefit from immunotherapy.

Keywords: Immunotherapy; leukemia; lymphoma; multiple myeloma (MM); tumor microenvironment (TME).

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Conflict of interest statement

Conflicts of Interest: AM Lesokhin: Stock or other ownership: Exelixis, Enumeral; Honoraria: Bristol-Myers Squibb, Janssen Pharmaceuticals (a Johnson & Johnson Co.), Gilead Sciences (I), Novartis; Consulting or advisory role: Bristol-Myers Squibb, Foundation Medicine (Inst), Janssen Pharmaceuticals (a Johnson & Johnson Co.), Novartis, Juno, Aduro; Research funding: Bristol-Myers Squibb (Inst), Janssen Pharmaceuticals (a Johnson & Johnson Co.) (Inst); Patents, royalties, other intellectual property: Serametrix. The other authors have no conflicts of interest to declare.

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References

    1. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell 2011;144:646-74. 10.1016/j.cell.2011.02.013 - DOI - PubMed
    1. Lesokhin AM, Callahan MK, Postow MA, et al. On being less tolerant: Enhanced cancer immunosurveillance enabled by targeting checkpoints and agonists of T cell activation. Sci Transl Med 2015;7:280sr1. 10.1126/scitranslmed.3010274 - DOI - PubMed
    1. Walunas TL, Lenschow DJ, Bakker CY, et al. CTLA-4 can function as a negative regulator of T cell activation. Immunity 1994;1:405-13. 10.1016/1074-7613(94)90071-X - DOI - PubMed
    1. Zou W, Chen L. Inhibitory B7-family molecules in the tumour microenvironment. Nat Rev Immunol 2008;8:467-77. 10.1038/nri2326 - DOI - PubMed
    1. Chen L, Han X. Anti-PD-1/PD-L1 therapy of human cancer: past, present, and future. J Clin Invest 2015;125:3384-91. 10.1172/JCI80011 - DOI - PMC - PubMed