Hypoproteinemia being a manifestation of immunotherapy-related liver dysfunction.
Hypoproteinemia
immunotherapy
liver dysfunction
lung cancer
programmed death-1/programmed death-ligand 1 inhibitor (PD-1/PD-L1 inhibitor)
Journal
Annals of translational medicine
ISSN: 2305-5839
Titre abrégé: Ann Transl Med
Pays: China
ID NLM: 101617978
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
entrez:
15
8
2020
pubmed:
15
8
2020
medline:
15
8
2020
Statut:
ppublish
Résumé
Immunotherapy has changed the pattern of treatment in cancer. The interaction between programmed death-1 (PD-1) and programmed death-ligand 1 (PD-L1) inhibits the activation of T cells, and PD-1/PD-L1 inhibitors can increase the immune response to cancer cells by inducing the immune cells, which has become an important clinical method to treat cancer. However, the alteration in the activation of T cells might lead to misidentification between the body's own cells and tumor cells and induce immune-related adverse events (IRAEs), such as pneumonitis, liver dysfunction, rash, colitis, nephritis, and endocrinopathies. And the IRAEs might lead to serious consequences. Studies have reported that PD-1/PD-L1 inhibitor-related hepatotoxicity is one of these adverse events. Most of the studies reported that hepatitis resulting from PD-1 inhibitor was manifested as elevated liver enzymes and bilirubin. Quite a few patients experienced lower degree of hepatotoxicity treated with checkpoint inhibitors, which indicated that it was necessary to focus on immunotherapy-related liver dysfunction. Here, we report a case of immunotherapy-related liver dysfunction with hypoproteinemia as the first manifestation under the treatment of PD-1 inhibitors combined with chemotherapy. This case suggests that hypoproteinemia was one of the manifestations of immunotherapy-related liver dysfunction, which helps us better understand the immunotherapy-related disease.
Identifiants
pubmed: 32793733
doi: 10.21037/atm-20-4980
pii: atm-08-14-889
pmc: PMC7396795
doi:
Types de publication
Case Reports
Langues
eng
Pagination
889Informations de copyright
2020 Annals of Translational Medicine. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-20-4980). The authors have no conflicts of interest to declare.
Références
Oncologist. 2016 Oct;21(10):1230-1240
pubmed: 27401894
Ann Rheum Dis. 2017 Jan;76(1):43-50
pubmed: 27307501
Hepatology. 2013 Nov;58(5):1836-46
pubmed: 23423799
J Thorac Dis. 2018 Feb;10(Suppl 3):S404-S411
pubmed: 29593886
J Immunother Cancer. 2019 Feb 18;7(1):47
pubmed: 30777137
Cancer Treat Rev. 2017 Jul;58:70-76
pubmed: 28689073
Endocr Relat Cancer. 2017 Dec;24(12):T331-T347
pubmed: 29025857
Front Pharmacol. 2017 Feb 08;8:49
pubmed: 28228726
J Immunother Cancer. 2017 Nov 21;5(1):95
pubmed: 29162153
J Dig Dis. 2016 Mar;17(3):193-201
pubmed: 26879902
J Hepatol. 2018 Jun;68(6):1181-1190
pubmed: 29427729
Crit Rev Oncol Hematol. 2017 Nov;119:1-12
pubmed: 29065979
PLoS One. 2016 Jul 29;11(7):e0160221
pubmed: 27472273
Invest New Drugs. 2017 Aug;35(4):529-536
pubmed: 28317087
Eur J Cancer. 2016 Feb;54:139-148
pubmed: 26765102
Best Pract Res Clin Rheumatol. 2018 Dec;32(6):781-802
pubmed: 31427055
Invest New Drugs. 2013 Aug;31(4):1071-7
pubmed: 23408334
BMC Med. 2015 Sep 04;13:211
pubmed: 26337719
Cell Res. 2018 Apr;28(4):433-447
pubmed: 29463898
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):4194-4201
pubmed: 31713435
Oncol Lett. 2017 Nov;14(5):5671-5680
pubmed: 29113194
Front Pharmacol. 2017 Oct 18;8:730
pubmed: 29093678
Cancer Immunol Res. 2017 Apr;5(4):312-318
pubmed: 28246107
Transl Lung Cancer Res. 2018 Apr;7(Suppl 2):S91-S94
pubmed: 29782565
Int J Mol Sci. 2017 Jul 13;18(7):
pubmed: 28703774
Transl Lung Cancer Res. 2019 Dec;8(6):1125-1133
pubmed: 32010590
J Crit Care. 2016 Jun;33:62-70
pubmed: 26831575
Cancer Immunol Res. 2018 Sep;6(9):1093-1099
pubmed: 29991499
J Oncol Pharm Pract. 2020 Mar;26(2):459-461
pubmed: 30909794