An algorithm based on immunotherapy discontinuation and liver biopsy spares corticosteroids in two thirds of cases of severe checkpoint inhibitor‐induced liver injury

Author:

Riveiro‐Barciela Mar123ORCID,Barreira‐Díaz Ana12ORCID,Salcedo María‐Teresa4,Callejo‐Pérez Ana5,Muñoz‐Couselo Eva5,Iranzo Patricia5,Ortiz‐Velez Carolina5,Cedrés Susana5,Díaz‐Mejía Nely5,Ruiz‐Cobo Juan Carlos12ORCID,Morales Rafael5,Aguilar‐Company Juan5,Zamora Ester5,Oliveira Mafalda5,Sanz‐Martínez María‐Teresa678,Viladomiu Lluis1,Martínez‐Gallo Mónica678,Felip Enriqueta5,Buti María123

Affiliation:

1. Department of Medicine Universitat Autònoma de Barcelona Barcelona Spain

2. Liver Unit, Internal Medicine Department Hospital Universitari Vall d'Hebron Barcelona Spain

3. CIBERehd, Instituto Carlos III Barcelona Spain

4. Human Pathology Department Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus Barcelona Spain

5. Oncology Department Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus Barcelona Spain

6. Immunology Division Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus Barcelona Spain

7. Translational Immunology Group Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Hospital Campus Barcelona Catalonia Spain

8. Department of Cell Biology, Physiology and Immunology Autonomous University of Barcelona (UAB) Barcelona Spain

Abstract

SummaryBackgroundThere are few data on corticosteroids (CS)‐sparing strategies for checkpoint inhibitor (ICI)‐induced liver injury (ChILI).AimWe aimed to assess the performance of a 2‐step algorithm for severe ChILI, based on ICI temporary discontinuation (step‐1) and, if lack of biochemical improvement, CS based on the degree of necroinflammation at biopsy (step‐2).MethodsProspective study that included all subjects with grade 3/4 ChILI. Peripheral extended immunophenotyping was performed. Indication for CS: severe necroinflammation; mild or moderate necroinflammation with later biochemical worsening.ResultsFrom 111 subjects with increased transaminases (January 2020 to August 2023), 44 were diagnosed with grade 3 (N = 35) or grade 4 (N = 9) ChILI. Main reason for exclusion was alternative diagnosis. Lung cancer (13) and melanoma (12) were the most common malignancies. ICI: 23(52.3%) anti‐PD1, 8(18.2%) anti‐PD‐L1, 3(6.8%) anti‐CTLA‐4, 10(22.7%) combined ICI. Liver injury pattern: hepatocellular (23,52.3%) mixed (12,27.3%) and cholestatic (9,20.5%). 14(32%) presented bilirubin >1.2 mg/dL. Overall, 30(68.2%) patients did not require CS: 22(50.0%) due to ICI discontinuation (step‐1) and 8/22 (36.4%) based on the degree of necroinflammation (step‐2). Biopsy mainly impacted on grade 3 ChILI, sparing CS in 8 out of 15 (53.3%) non‐improvement patients after ICI discontinuation. CD8+ HLA‐DR expression (p = 0.028), central memory (p = 0.046) were lower in CS‐free managed subjects, but effector‐memory cells (p = 0.002) were higher. Time to transaminases normalisation was shorter in those CS‐free managed (overall: p < 0.001, grade 3: p < 0.001). Considering our results, a strategy based on ICI discontinuation and biopsy for grade 3 ChILI is proposed.ConclusionsAn algorithm based on temporary immunotherapy discontinuation and biopsy allows CS avoidance in two thirds of cases of severe ChILI.

Publisher

Wiley

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