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[Pathological features of immune-mediated hepatitis due to immune checkpoint inhibitors and anti-angiogenesis targeted therapy].
Zhang, Q Y; Chen, L L; Gao, F; Sujie, Akesu; Hou, Y Y; Huang, X W; Huang, C; Sun, H C; Zhou, J; Ji, Y.
Afiliación
  • Zhang QY; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Chen LL; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Gao F; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Sujie A; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Hou YY; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Huang XW; Department of Liver Surgery, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Huang C; Department of Liver Surgery, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Sun HC; Department of Liver Surgery, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Zhou J; Department of Liver Surgery, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
  • Ji Y; Department of Pathology, Zhongshan Hospital of Fudan University, Shanghai 200032, China.
Zhonghua Bing Li Xue Za Zhi ; 49(4): 329-335, 2020 Apr 08.
Article en Zh | MEDLINE | ID: mdl-32268669
ABSTRACT

Objective:

To compare the histologic features of immune-mediated hepatitis (IMH) due to immune checkpoint inhibitors (ICIs) monotherapy and combined ICIs anti-angiogenesis tyrosine kinases (TKIs) targeted therapy.

Methods:

Twenty-one IMH patients who had liver biopsy during ICIs treatment in Zhongshan Hospital of Fudan University from 2015 to 2019 were included. Among them, ten were treated with ICIs monotherapy, and 11 were treated with combined ICIs and anti-angiogenesis targeted therapy. The histologic features of IMH were assessed by HE staining and PD-L1/2 was evaluated by immunohistochemical staining.

Results:

Patients treated with monotherapy ICIs presented with different levels of lobular hepatitis and portal inflammation. Besides, there were also cholangitis, endothelialitis, Kupffer cells activation and peliosisi hepatitis. Eight cases (8/10) showed mild and two cases (2/10) showed moderate hepatic injury. As for patients receiving combined ICIs and TKIs therapy, the extent of IMH was more severe, with four cases (4/11) showing moderate-severe liver injury, with confluent or bridging necrosis, portal inflammation, cholangitis, interface hepatitis. Among these, one patient developed acute severe hepatitis with massive hepatocyte necrosis and died of multisystem dysfunction. In those cases with severe liver injury, many CD8 positive lymphocytes aggregated in the portal area and hepatic sinusoid, and PD-L1 was expressed in many endothelial cells. There were both 2 cases of death in ICIs monotherapy and combination therapy group. Among the latter group, 1 patient developed acute severe hepatitis with massive hepatocyte necrosis and died of multisystem dysfunction.

Conclusion:

Compared with ICIs monotherapy, combined ICIs and anti-angiogenesis targeted TKIs therapy may cause overlapping hepatic injury, leading to severe IMH.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Endoteliales / Hepatitis / Antineoplásicos Límite: Humans Idioma: Zh Revista: Zhonghua Bing Li Xue Za Zhi Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Endoteliales / Hepatitis / Antineoplásicos Límite: Humans Idioma: Zh Revista: Zhonghua Bing Li Xue Za Zhi Año: 2020 Tipo del documento: Article País de afiliación: China