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Review
. 2018 Sep 20:9:1050.
doi: 10.3389/fphar.2018.01050. eCollection 2018.

Prognostic Factors for Checkpoint Inhibitor Based Immunotherapy: An Update With New Evidences

Affiliations
Review

Prognostic Factors for Checkpoint Inhibitor Based Immunotherapy: An Update With New Evidences

Xinyu Yan et al. Front Pharmacol. .

Abstract

Checkpoint inhibitor (CPI) based immunotherapy (i.e., anit-CTLA-4/PD-1/PD-L1 antibodies) can effectively prolong overall survival of patients across several cancer types at the advanced stage. However, only part of patients experience objective responses from such treatments, illustrating large individual differences in terms of both efficacy and adverse drug reactions. Through the observation on a series of CPI based clinical trials in independent patient cohorts, associations of multiple clinical and molecular characteristics with CPI response rate have been determined, including microenvironment, genomic alterations of the cancer cells, and even gut microbiota. A broad interest has been drawn to the question whether and how these prognostic factors can be used as biomarkers for optimal usage of CPIs in precision immunotherapy. Therefore, we reviewed the candidate prognostic factors identified by multiple trials and the experimental investigations, especially those reported in the recent 2 years, and described the possibilities and problems of them in routine clinical usage of cancer treatment as biomarkers.

Keywords: CTLA-4; PD-1; PD-L1; checkpoint inhibitor; immunotherapy.

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Figures

FIGURE 1
FIGURE 1
Factors associated with response to anti-PD-1/PD-L1 therapy.

References

    1. Akbay E. A., Koyama S., Carretero J., Altabef A., Tchaicha J. H., Christensen C. L., et al. (2013). Activation of the PD-1 pathway contributes to immune escape in EGFR-driven lung tumors. Cancer Discov. 3 1355–1363. 10.1158/2159-8290.CD-13-0310 - DOI - PMC - PubMed
    1. Aptsiauri N., Cabrera T., Garcia-Lora A., Lopez-Nevot M. A., Ruiz-Cabello F., Garrido F. (2007). MHC class I antigens and immune surveillance in transformed cells. Int. Rev. Cytol. 256 139–189. 10.1016/S0074-7696(07)56005-5 - DOI - PubMed
    1. Armand P., Nagler A., Weller E. A., Devine S. M., Avigan D. E., Chen Y. B., et al. (2013). Disabling immune tolerance by programmed death-1 blockade with pidilizumab after autologous hematopoietic stem-cell transplantation for diffuse large B-cell lymphoma: results of an international phase II trial. J. Clin. Oncol. 31 4199–4206. 10.1200/JCO.2012.48.3685 - DOI - PMC - PubMed
    1. Ascierto M. L., Makohon-Moore A., Lipson E. J., Taube J. M., McMiller T. L., Berger A. E., et al. (2017). Transcriptional mechanisms of resistance to anti-PD-1 therapy. Clin. Cancer Res. 23 3168–3180. 10.1158/1078-0432.CCR-17-0270 - DOI - PMC - PubMed
    1. Bagley S. J., Kothari S., Aggarwal C., Bauml J. M., Alley E. W., Evans T. L., et al. (2017). Pretreatment neutrophil-to-lymphocyte ratio as a marker of outcomes in nivolumab-treated patients with advanced non-small-cell lung cancer. Lung. Cancer 106 1–7. 10.1016/j.lungcan.2017.01.013 - DOI - PubMed