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Evolution of liver function during immune checkpoint inhibitor treatment for hepatocellular carcinoma.
Pomej, Katharina; Balcar, Lorenz; Sidali, Sabrina; Sartoris, Riccardo; Meischl, Tobias; Trauner, Michael; Mandorfer, Mattias; Reiberger, Thomas; Ronot, Maxime; Bouattour, Mohamed; Pinter, Matthias; Scheiner, Bernhard.
Afiliação
  • Pomej K; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Balcar L; Liver Cancer (HCC) Study Group Vienna, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Sidali S; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Sartoris R; Liver Cancer (HCC) Study Group Vienna, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Meischl T; Department of Digestive Oncology, APHP.Nord, Hôpital Beaujon, Clichy, France.
  • Trauner M; Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, France.
  • Mandorfer M; Liver Cancer (HCC) Study Group Vienna, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Reiberger T; Division of Hematology and Oncology, Department of Internal Medicine III, Hanusch Hospital, Vienna, Austria.
  • Ronot M; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Bouattour M; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Pinter M; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Scheiner B; Department of Radiology, APHP.Nord, Hôpital Beaujon, Clichy, France.
Article em En | MEDLINE | ID: mdl-38990728
ABSTRACT
BACKGROUND AND

AIMS:

Deterioration of liver function is a leading cause of death in patients with advanced hepatocellular carcinoma (HCC). We evaluated the impact of immune checkpoint inhibitor (ICI)-treatment on liver function and outcomes.

METHOD:

HCC patients receiving ICIs or sorafenib between 04/2003 and 05/2024 were included. Liver function (assessed by Child-Pugh score [CPS]) was evaluated at the start of ICI-treatment (baseline, BL) and 3 and 6 months thereafter. A ≥1 point change in CPS was defined as deterioration (-) or improvement (+), while equal CPS points were defined as stable (=).

RESULTS:

Overall, 182 ICI-treated patients (66.8 ± 11.8 years; cirrhosis n = 134, 74%) were included. At BL, median CPS was 5 (IQR 5-6; CPS-A 147, 81%). After 3 months, liver function improved/stabilized in 102 (56%) and deteriorated in 61 (34%) patients, while 19 (10%) patients deceased/had missing follow-up (d/noFU). Comparable results were observed at 6 months (+/= n = 82, 45%; - n = 55, 30%; d/noFU n = 45, 25%). In contrast, 54 (34%) and 33 (21%) out of 160 sorafenib patients achieved improvement/stabilization at 3 and 6 months, respectively. Radiological response was linked to CPS improvement/stabilization at 6 months (responders vs. non-responders, 73% vs. 50%; p = 0.007). CPS improvement/stabilization at 6 months was associated with better overall survival following landmark analysis (6 months +/= 28.4 [95% CI 18.7-38.1] versus - 14.2 [95% CI 10.3-18.2] months; p < 0.001). Of 35 ICI-patients with CPS-B at BL, improvement/stabilization occurred in 16 (46%) patients, while 19 (54%) patients deteriorated/d/noFU at 3 months. Comparable results were observed at 6 months (CPS +/= 14, 40%, - 8, 23%). Importantly, 6/35 (17%) and 9/35 (26%) patients improved from CPS-B to CPS-A at 3 and 6 months.

CONCLUSION:

Radiological response to ICI-treatment was associated with stabilization or improvement in liver function, which correlated with improved survival, even in patients with Child-Pugh class B at baseline.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article