Preview

Clinical Case in Oncology

Advanced search

Immune-mediated hepatitis. A literature review

https://doi.org/10.62546/3034-1477-2026-4-1-21-00

Abstract

Aim. Immune checkpoint inhibitors (ICIs) have transformed the standards of systemic therapy across a broad range of malignancies; however, the expansion of their indications has inevitably been accompanied by a rise in immunerelated adverse events. The aim of this review is to summarise current understanding of the pathogenesis, clinical presentation, incidence, differential diagnosis and management of immune-mediated hepatitis associated with immune checkpoint inhibitor therapy, comparing the approaches adopted by international and Russian professional societies.
Methods. Publications were searched in PubMed/MEDLINE and eLIBRARY, as well as on the official websites of the professional societies ASCO (American Society of Clinical Oncology), ESMO (European Society for Medical Oncology), RUSSCO (Russian Society of Clinical Oncology) and NCCN (National Comprehensive Cancer Network), and of regulatory agencies (FDA Food and Drug Administration). Current clinical guidelines, official prescribing information, systematic reviews, meta-analyses, randomised trials and real-world data were included. Results. The liver ranks third among the organs affected, after the skin and the gastrointestinal tract. According to the integrated safety databases of regulatory agencies, the incidence of immune-mediated hepatitis was 0.7% for pembrolizumab, 1.8% for nivolumab and atezolizumab, 2.8% for durvalumab, and 7.0 to 15.0% for nivolumab combined with ipilimumab, depending on the dose ratio. PD-1 inhibitors were associated with more frequent transaminase elevations than PD-L1 inhibitors. Management is based on stepwise immunosuppression; mycophenolate mofetil is the second-line agent, whereas infliximab is not used in hepatic involvement.
Conclusion. Immune-mediated hepatitis requires differential diagnosis, since a substantial proportion of liver test elevations is due to alternative causes. The extent of immunosuppression should be matched to the clinical severity of the condition rather than to the formal CTCAE grade alone.

About the Authors

R. V. Orlova
St. Petersburg City Clinical Oncology Dispensary; St. Petersburg State University
Russian Federation


I. M. Itkin
St. Petersburg City Clinical Oncology Dispensary
Russian Federation


А. К. Ivanova
St. Petersburg City Clinical Oncology Dispensary
Russian Federation


K. K. Kutcher
St. Petersburg City Clinical Oncology Dispensary
Russian Federation


References

1. Schneider B.J., Naidoo J., Santomasso B.D. et al. Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: ASCO Guideline Update. J. Clin. Oncol. 2021; 39 (36): 4073–4126. doi: 10.1200/JCO.21.01440.

2. Liu Z., Zhu Y., Xie H., Zou Z. Immune-mediated hepatitis induced by immune checkpoint inhibitors: current updates and future perspectives. Front Pharmacol . 2023; 13: 1077468. doi: 10.3389/fphar.2022.1077468.

3. Новик А.В., Баллюзек М.Ф., Васильев Д.А. и др. Иммуноопосредованные нежелательные явления. Клинические рекомендации RUSSCO, часть 2. Злокачественные опухоли. 2025; 15 (3s2): 271–329. rosoncoweb.ru/standarts/RUSSCO/2025/2025-2-16.pdf.

4. Wang D.Y., Salem J.E., Cohen J.V. et al. Fatal toxic effects associated with immune checkpoint inhibitors: a systematic review and meta-analysis. JAMA Oncol . 2018; 4 (12): 1721–1728. doi: 10.1001/jamaoncol.2018.3923.

5. Cunningham M., Gupta R., Butler M. Checkpoint inhibitor hepatotoxicity: pathogenesis and management. Hepatology . 2024; 79 (1): 198–212. doi: 10.1097/HEP.0000000000000045.

6. Swanson L.A., Hawa F., Fontana R.J. Immune-mediated liver injury from checkpoint inhibitors: best practices in 2024. Hepatol. Commun . 2024. PMID: 38841193. pmc.ncbi.nlm.nih.gov/articles/PMC11152778.

7. Dara L., De Martin E. Immune-mediated liver injury from checkpoint inhibitor: an evolving frontier with emerging challenges. Liver Int . 2025; 45 (2): e16198. doi: 10.1111/liv.16198

8. Gudd C.L.C., Au L., Triantafyllou E. et al. Activation and transcriptional profile of monocytes and CD8+ T cells are altered in checkpoint inhibitor-related hepatitis. J. Hepatol . 2021; 75 (1): 177–189. doi: 10.1016/j.jhep.2021.02.008.

9. Gudd C.L.C., Mitchell E., Atkinson S.R. et al. Therapeutic inhibition of monocyte recruitment prevents checkpoint inhibitor-induced hepatitis. J. Immunother. Cancer . 2024; 12 (4): e008078. doi: 10.1136/jitc-2023-008078.

10. De Martin E., Michot J.M., Papouin B. et al. Characterization of liver injury induced by cancer immunotherapy using immune checkpoint inhibitors. J. Hepatol. 2018; 68 (6): 1181–1190. doi: 10.1016/j.jhep.2018.01.033.

11. Parlati L., Sakka M., Retbi A. et al. Burden of grade 3 or 4 liver injury associated with immune checkpoint inhibitors. JHEP Rep. 2023; 5 (12): 100880. doi: 10.1016/j.jhepr.2023.100880.

12. Hountondji L., Ferreira De Matos C., Lebossé F. et al. Clinical pattern of checkpoint inhibitor-induced liver injury in a multicentre cohort. JHEP Rep . 2023; 5 (6): 100719. doi: 10.1016/j.jhepr.2023.100719.

13. OPDIVO (nivolumab). Highlights of Prescribing Information. U.S. Food and Drug Administration, 2024. accessdata.fda.gov инструкция OPDIVO.

14. Haanen J., Obeid M., Spain L. et al. Management of toxicities from immunotherapy: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann. Oncol . 2022; 33 (12): 1217–1238. doi: 10.1016/j.annonc.2022.10.001.

15. Zhou X., Yao Z., Bai H. et al. Treatment-related adverse events of PD-1 and PD-L1 inhibitor-based combination therapies in clinical trials: a systematic review and meta-analysis. Lancet Oncol. 2021; 22 (9): 1265–1274. doi: 10.1016/S1470-2045(21)00333-8.

16. Fu J., Li W.-Z., McGrath N.A., Lai C.W., Brar G., Xiang Y.-Q., Xie C. Immune checkpoint inhibitor associated hepatotoxicity in primary liver cancer versus other cancers: a systematic review and meta-analysis. Front Oncol . 2021; 11: 650292. doi: 10.3389/fonc.2021.650292.

17. KEYTRUDA (pembrolizumab). Highlights of Prescribing Information. U.S. Food and Drug Administration, 2024. accessdata.fda.gov инструкция KEYTRUDA.

18. TECENTRIQ (atezolizumab). Prescribing Information and Important Safety Information. Genentech, 2025. tecentriq-hcp.com.

19. IMFINZI (durvalumab). Prescribing Information and Important Safety Information. AstraZeneca, 2025. astrazenecaus.com информация по безопасности IMFINZI.

20. Camrelizumab: сведения о безопасности регистрационного досье (Национальное управление медицинской продукции КНР), приведенные в протоколе клинического исследования NCT04649476. clinicaltrials.gov протокол NCT04649476.

21. Bellmunt J., Hussain M., Gschwend J.E. et al. Adjuvant atezolizumab versus observation in muscle-invasive urothelial carcinoma (IMvigor010): a multicentre, open-label, randomised, phase 3 trial. Lancet Oncol . 2021; 22 (4): 525–537. doi: 10.1016/S1470-2045 (21)00004-8.

22. Powles T., van der Heijden M.S., Castellano D. et al. Durvalumab alone and durvalumab plus tremelimumab versus chemotherapy in previously untreated patients with unresectable, locally advanced or metastatic urothelial carcinoma (DANUBE): a randomised, open-label, multicentre, phase 3 trial. Lancet Oncol . 2020; 21 (12): 1574–1588. doi: 10.1016/S1470-2045 (20)30541-6.

23. Qin S., Ren Z., Meng Z. et al. Camrelizumab in patients with previously treated advanced hepatocellular carcinoma: a multicentre, open-label, parallel-group, randomised, phase 2 trial. Lancet Oncol . 2020; 21 (4): 571–580. doi: 10.1016/S1470-2045 (20)30011-5.

24. Rakké Y.S., Buschow S.I., IJzermans J.N.M., Sprengers D. Camrelizumab: targeting a novel PD-1 epitope to treat hepatocellular carcinoma. Ann. Transl. Med . 2020; 8 (21): 1338. doi: 10.21037/atm-20-4306.

25. Wang K., Li B., Li M. et al. The safety and efficacy of camrelizumab and its combination with apatinib in various solid cancers. Front Pharmacol. 2020; 11: 568477. doi: 10.3389/fphar.2020.568477.

26. Li L., Li G., Rao B. et al. Landscape of immune checkpoint inhibitor-related adverse events in Chinese population. Sci Rep . 2020; 10:15567. doi: 10.1038/s41598-020-72649-5.

27. Celsa C., Cabibbo G., Fulgenzi C.A.M. et al. Characteristics and outcomes of immunotherapy-related liver injury in patients with hepatocellular carcinoma versus other advanced solid tumours. J. Hepatol. 2024; 80 (3): 431–442. doi: 10.1016/j.jhep.2023.10.040.

28. Yau T., Kang Y.K., Kim T.Y. et al. Efficacy and safety of nivolumab plus ipilimumab in patients with advanced hepatocellular carcinoma previously treated with sorafenib: the CheckMate 040 randomized clinical trial. JAMA Oncol. 2020; 6 (11): e204564. doi: 10.1001/jamaoncol.2020.4564.

29. Zhu A.X., Finn R.S., Edeline J. et al. Pembrolizumab in patients with advanced hepatocellular carcinoma previously treated with sorafenib (KEYNOTE-224): a non-randomised, open-label phase 2 trial. Lancet Oncol . 2018; 19 (7): 940952. doi: 10.1016/S1470-2045(18)30351-6.

30. Finn R.S., Ryoo B.Y., Merle P. et al. Pembrolizumab as second-line therapy in patients with advanced hepatocellular carcinoma in KEYNOTE-240: a randomized, double-blind, phase III trial. J. Clin. Oncol. 2020; 38 (3): 193–202. doi: 10.1200/JCO.19.01307.

31. Pu D., Yin L., Zhou Y. et al. Safety and efficacy of immune checkpoint inhibitors in patients with HBV/HCV infection and advanced-stage cancer: a systematic review. Medicine (Baltimore) . 2020; 99 (5): e19013. doi: 10.1097/MD.0000000000019013.

32. Severity Grading in Drug Induced Liver Injury. In: LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; обновлено 4 мая 2019. PMID: 31643566. ncbi.nlm.nih.gov/books/NBK548241.

33. Chalasani N., Bonkovsky H.L., Fontana R. et al. Features and outcomes of 899 patients with drug-induced liver injury: the DILIN prospective study. Gastroenterology . 2015; 148 (7): 1340–1352. gastrojournal.org DILIN Prospective Study.

34. Fontana R.J., Liou I., Reuben A. et al. AASLD practice guidance on drug, herbal, and dietary supplement-induced liver injury. Hepatology . 2023. pmc.ncbi.nlm.nih.gov/articles/PMC9936988.

35. European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Drug-induced liver injury. J. Hepatol. 2019; 70 (6): 1222–1261. doi: 10.1016/j.jhep.2019.02.014.

36. Tsung I., Dolan R., Lao C.D. et al. Liver injury is most commonly due to hepatic metastases rather than drug hepatotoxicity during pembrolizumab immunotherapy. Aliment. Pharmacol. Ther. 2019; 50 (7): 800–808. doi: 10.1111/apt.15413.

37. NCCN Clinical Practice Guidelines in Oncology. Management of Immunotherapy-Related Toxicities. Version 1.2026. National Comprehensive Cancer Network, 2026.

38. Dougan M., Wang Y., Rubio-Tapia A., Lim J.K. AGA Clinical Practice Update on diagnosis and management of immune checkpoint inhibitor colitis and hepatitis: expert review. Gastroenterology . 2021; 160 (4): 1384–1393. doi: 10.1053/j.gastro.2020.08.063.

39. Brahmer J.R., Abu-Sbeih H., Ascierto P.A. et al. Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immune checkpoint inhibitor-related adverse events. J. Immunother Cancer . 2021; 9 (6): e002435. doi: 10.1136/jitc-2021-002435.

40. Gauci M.L., Baroudjian B., Zeboulon C. et al. Immune-related hepatitis with immunotherapy: are corticosteroids always needed? J. Hepatol . 2018; 69 (2): 548–550. doi: 10.1016/j.jhep.2018.03.034.

41. Li M., Wong D., Vogel A.S. et al. Effect of corticosteroid dosing on outcomes in high-grade immune checkpoint inhibitor hepatitis. Hepatology . 2022; 75 (3): 531–540. doi: 10.1002/hep.32215.

42. Rosario Lora D., Post Z., Reau N.S. Immune checkpoint inhibitor-related hepatitis: beyond the guidelines. World Gastroenterology Organisation, e-WGN . 2025; 30 (3). worldgastroenterology.org e-WGN Expert Point of View.

43. Ziemer M., Koukoulioti E., Beyer S. et al. Managing immune checkpoint-inhibitor-induced severe autoimmune-like hepatitis using liver-directed steroids. J. Hepatol. 2017; 66 (3): 657–659. doi: 10.1016/j.jhep.2016.11.015.

44. Hwang S.Y., Hsieh P., Zhang W. Steroid-refractory immune checkpoint inhibitor hepatitis and ICI rechallenge: a systematic review and meta-analysis. Hepatol. Commun . 2024; 8 (10): e0525. doi: 10.1097/HC9.0000000000000525.

45. Peeraphatdit T.B., Wang J., Odenwald M.A. et al. Hepatotoxicity from immune checkpoint inhibitors: a systematic review and management recommendation. Hepatology . 2020; 72 (1): 315–329. doi: 10.1002/hep.31227.

46. Shimoda-Igawa Y., Yoshida T., Yoshinami Y. et al. Early combination with mycophenolate mofetil for immune-related hepatitis in patients with solid tumors treated with immune checkpoint inhibitors. J. Clin. Oncol . 2024; 42 (16_suppl): 12133 (ASCO Annual Meeting). doi: 10.1200/JCO.2024.42.16_suppl.12133.

47. Mair M.J., Weiss L., Batchelor T. et al. Tocilizumab as prophylaxis for immune-related adverse events associated with checkpoint inhibitor therapy: first results from the randomized, placebo-controlled phase II trial TICIMEL. J. Clin. Oncol. 2024; 42 (16_suppl): 9553. doi: 10.1200/JCO.2024.42.16_suppl.9553.

48. Moi M., Özluk A.A., Gunenc D. et al. Tocilizumab in grade 4 steroid-refractory ICI-hepatitis: case series and literature review. Clin. Liver Dis. 2024; 18 (6): 1770–1774. doi: 10.1007/s12072-024-10688-0.

49. Riveiro-Barciela M., Barreira-Díaz A., Callejo-Pérez A. et al. Retreatment with immune checkpoint inhibitors after a severe immune-related hepatitis: results from a prospective multicenter study. Clin. Gastroenterol. Hepatol. 2023; 21 (3): 732–740. doi: 10.1016/j.cgh.2022.03.050.

50. Dolladille C., Ederhy S., Sassier M. et al. Immune checkpoint inhibitor rechallenge after immune-related adverse events in patients with cancer. JAMA Oncol . 2020; 6 (6): 865–871. doi: 10.1001/jamaoncol.2020.0726.


Review

For citations:


Orlova R.V., Itkin I.M., Ivanova А.К., Kutcher K.K. Immune-mediated hepatitis. A literature review. Clinical Case in Oncology. 2026;4(1):21-39. (In Russ.) https://doi.org/10.62546/3034-1477-2026-4-1-21-00

Views: 15

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 3034-1477 (Print)
ISSN 3034-4018 (Online)