TY - JOUR
T1 - Atezolizumab/bevacizumab and lenvatinib for hepatocellular carcinoma
T2 - A comparative analysis in a European real-world cohort
AU - de Castro, Tiago
AU - Welland, Sabrina
AU - Jochheim, Leonie
AU - Leyh, Cathrine
AU - Shmanko, Kateryna
AU - Finkelmeier, Fabian
AU - Jeliazkova, Petia
AU - Jefremow, Andre
AU - Gonzalez-Carmona, Maria A
AU - Kandulski, Arne
AU - Roessler, Daniel
AU - Ben Khaled, Najib
AU - Enssle, Stefan
AU - Venerito, Marino
AU - Fründt, Thorben W
AU - Schultheiß, Michael
AU - Djanani, Angela
AU - Pangerl, Maria
AU - Maieron, Andreas
AU - Wirth, Thomas C
AU - Marquardt, Jens U
AU - Greil, Richard
AU - Fricke, Christina
AU - Günther, Rainer
AU - Schmiderer, Andreas
AU - Bettinger, Dominik
AU - Wege, Henning
AU - Scheiner, Bernhard
AU - Müller, Martina
AU - Strassburg, Christian P
AU - Siebler, Jürgen
AU - Ehmer, Ursula
AU - Waidmann, Oliver
AU - Weinmann, Arndt
AU - Pinter, Matthias
AU - Lange, Christian M
AU - Saborowski, Anna
AU - Vogel, Arndt
N1 - Publisher Copyright:
© 2024 The Author(s).
PY - 2024/11/1
Y1 - 2024/11/1
N2 - BACKGROUND: Immunotherapy-based combinations are currently the standard of care in the systemic treatment of patients with HCC. Recent studies have reported unexpectedly long survival with lenvatinib (LEN), supporting its use in first-line treatment for HCC. This study aims to compare the real-world effectiveness of LEN to atezolizumab/bevacizumab (AZ/BV).METHODS: A retrospective analysis was conducted to evaluate the effectiveness and safety of frontline AZ/BV or LEN therapy in patients with advanced HCC across 18 university hospitals in Europe.RESULTS: The study included 412 patients (AZ/BV: n=207; LEN: n=205). Baseline characteristics were comparable between the 2 treatment groups. However, patients treated with AZ/BV had a significantly longer median progression-free survival compared to those receiving LEN. The risk of hepatic decompensation was significantly higher in patients with impaired baseline liver function (albumin-bilirubin [ALBI] grade 2) treated with AZ/BV compared to those with preserved liver function. Patients with alcohol-associated liver disease had poorer baseline liver function compared to other etiologies and exhibited a worse outcome under AZ/BV.CONCLUSIONS: In this real-world cohort, survival rates were similar between patients treated with LEN and those treated with AZ/BV, confirming that both are viable first-line options for HCC. The increased risk of hepatic decompensation in patients treated with AZ/BV who have impaired baseline liver function underscores the need for careful monitoring. Future trials should aim to distinguish more clearly between metabolic dysfunction-associated steatotic liver disease and alcohol-associated liver disease.
AB - BACKGROUND: Immunotherapy-based combinations are currently the standard of care in the systemic treatment of patients with HCC. Recent studies have reported unexpectedly long survival with lenvatinib (LEN), supporting its use in first-line treatment for HCC. This study aims to compare the real-world effectiveness of LEN to atezolizumab/bevacizumab (AZ/BV).METHODS: A retrospective analysis was conducted to evaluate the effectiveness and safety of frontline AZ/BV or LEN therapy in patients with advanced HCC across 18 university hospitals in Europe.RESULTS: The study included 412 patients (AZ/BV: n=207; LEN: n=205). Baseline characteristics were comparable between the 2 treatment groups. However, patients treated with AZ/BV had a significantly longer median progression-free survival compared to those receiving LEN. The risk of hepatic decompensation was significantly higher in patients with impaired baseline liver function (albumin-bilirubin [ALBI] grade 2) treated with AZ/BV compared to those with preserved liver function. Patients with alcohol-associated liver disease had poorer baseline liver function compared to other etiologies and exhibited a worse outcome under AZ/BV.CONCLUSIONS: In this real-world cohort, survival rates were similar between patients treated with LEN and those treated with AZ/BV, confirming that both are viable first-line options for HCC. The increased risk of hepatic decompensation in patients treated with AZ/BV who have impaired baseline liver function underscores the need for careful monitoring. Future trials should aim to distinguish more clearly between metabolic dysfunction-associated steatotic liver disease and alcohol-associated liver disease.
KW - Humans
KW - Carcinoma, Hepatocellular/drug therapy
KW - Liver Neoplasms/drug therapy
KW - Quinolines/therapeutic use
KW - Male
KW - Antibodies, Monoclonal, Humanized/therapeutic use
KW - Phenylurea Compounds/therapeutic use
KW - Female
KW - Retrospective Studies
KW - Aged
KW - Middle Aged
KW - Bevacizumab/therapeutic use
KW - Europe
KW - Progression-Free Survival
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
UR - http://www.scopus.com/inward/record.url?scp=85208982875&partnerID=8YFLogxK
U2 - 10.1097/HC9.0000000000000562
DO - 10.1097/HC9.0000000000000562
M3 - Journal article
C2 - 39495153
SN - 2471-254X
VL - 8
JO - Hepatology Communications
JF - Hepatology Communications
IS - 11
M1 - e0562
ER -