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Survival outcomes from atezolizumab plus bevacizumab versus Lenvatinib in Child Pugh B unresectable hepatocellular carcinoma patients.
Rimini, Margherita; Persano, Mara; Tada, Toshifumi; Suda, Goki; Shimose, Shigeo; Kudo, Masatoshi; Cheon, Jaekyung; Finkelmeier, Fabian; Lim, Ho Yeong; Presa, José; Salani, Francesca; Lonardi, Sara; Piscaglia, Fabio; Kumada, Takashi; Sakamoto, Naoya; Iwamoto, Hideki; Aoki, Tomoko; Chon, Hong Jae; Himmelsbach, Vera; Schirripa, Marta; Montes, Margarida; Vivaldi, Caterina; Soldà, Caterina; Hiraoka, Atsushi; Sho, Takuya; Niizeki, Takashi; Nishida, Naoshi; Steup, Christoph; Hirooka, Masashi; Kariyama, Kazuya; Tani, Joji; Atsukawa, Masanori; Takaguchi, Koichi; Itobayashi, Ei; Fukunishi, Shinya; Tsuji, Kunihiko; Ishikawa, Toru; Tajiri, Kazuto; Ochi, Hironori; Yasuda, Satoshi; Toyoda, Hidenori; Ogawa, Chikara; Nishimura, Takashi; Hatanaka, Takeshi; Kakizaki, Satoru; Shimada, Noritomo; Kawata, Kazuhito; Tada, Fujimasa; Ohama, Hideko; Nouso, Kazuhiro.
Afiliação
  • Rimini M; Department of Oncology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientific Institute Hospital, Milan, Italy. margherita.rimini@gmail.com.
  • Persano M; Department of Oncology, IRCCS San Raffaele Hospital, Milan, Italy. margherita.rimini@gmail.com.
  • Tada T; Medical Oncology, University and University Hospital of Cagliari, Cagliari, Italy.
  • Suda G; Department of Internal Medicine, Japanese Red Cross Himeji Hospital, Himeji, Japan.
  • Shimose S; Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, North 15, West 7, Kita-Ku, Sapporo, Hokkaido, 060-8638, Japan.
  • Kudo M; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, 830-0011, Japan.
  • Cheon J; Department of Gastroenterology and Hepatology, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.
  • Finkelmeier F; Department of Medical Oncology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Republic of Korea.
  • Lim HY; Department of Internal Medicine 1, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
  • Presa J; Department of Medicine, School of Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul, South Korea.
  • Salani F; Unidade de Hepatologia, CHTMAD, Vila Real, Portugal.
  • Lonardi S; Unit of Medical Oncology 2, University Hospital of Pisa, Pisa, Italy.
  • Piscaglia F; Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
  • Kumada T; Oncology Unit 1, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
  • Sakamoto N; Division of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Iwamoto H; Department of Nursing, Gifu Kyoritsu University, Ogaki, Japan.
  • Aoki T; Department of Internal Medicine, Japanese Red Cross Himeji Hospital, Himeji, Japan.
  • Chon HJ; Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, North 15, West 7, Kita-Ku, Sapporo, Hokkaido, 060-8638, Japan.
  • Himmelsbach V; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, 830-0011, Japan.
  • Schirripa M; Department of Gastroenterology and Hepatology, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.
  • Montes M; Department of Medical Oncology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Republic of Korea.
  • Vivaldi C; Medical Oncology Unit, Department of Oncology and Hematology, Central Hospital of Belcolle, Strada Sammartinese Snc, 01100, Viterbo, Italy.
  • Soldà C; Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.
  • Hiraoka A; Department of Medicine, School of Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul, South Korea.
  • Sho T; Unidade de Hepatologia, CHTMAD, Vila Real, Portugal.
  • Niizeki T; Unit of Medical Oncology 2, University Hospital of Pisa, Pisa, Italy.
  • Nishida N; Oncology Unit 1, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
  • Steup C; Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Ehime, Japan.
  • Hirooka M; Department of Internal Medicine, Japanese Red Cross Himeji Hospital, Himeji, Japan.
  • Kariyama K; Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, North 15, West 7, Kita-Ku, Sapporo, Hokkaido, 060-8638, Japan.
  • Tani J; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, 830-0011, Japan.
  • Atsukawa M; Department of Medical Oncology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Republic of Korea.
  • Takaguchi K; Department of Gastroenterology, Okayama City Hospital, Okayama, Japan.
  • Itobayashi E; Department of Gastroenterology and Hepatology, Kagawa University, Kagawa, Japan.
  • Fukunishi S; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan.
  • Tsuji K; Department of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
  • Ishikawa T; Department of Gastroenterology, Asahi General Hospital, Asahi, Japan.
  • Tajiri K; Department of Gastroenterology, Osaka Medical and Pharmaceutical University, Osaka, Japan.
  • Ochi H; Center of Gastroenterology, Teine Keijinkai Hospital, Sapporo, Japan.
  • Yasuda S; Department of Gastroenterology, Saiseikai Niigata Hospital, Niigata, Japan.
  • Toyoda H; Department of Gastroenterology, Toyama University Hospital, Toyama, Japan.
  • Ogawa C; Hepato-Biliary Center, Japanese Red Cross Matsuyama Hospital, Matsuyama, Japan.
  • Nishimura T; Department of Gastroenterology and Hepatology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Hatanaka T; Department of Gastroenterology, Japanese Red Cross Takamatsu Hospital, Takamatsu, Japan.
  • Kakizaki S; Department of Gastroenterology, Japanese Red Cross Takamatsu Hospital, Takamatsu, Japan.
  • Shimada N; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Hyogo Medical University, Nishinomiya, Japan.
  • Kawata K; Department of Gastroenterology, Gunma Saiseikai Maebashi Hospital, Maebashi, Japan.
  • Tada F; Department of Clinical Research, National Hospital Organization Takasaki General Medical Center, Takasaki, Japan.
  • Ohama H; Division of Gastroenterology and Hepatology, Otakanomori Hospital, Kashiwa, Japan.
  • Nouso K; Department of Hepatology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
J Cancer Res Clin Oncol ; 149(10): 7565-7577, 2023 Aug.
Article em En | MEDLINE | ID: mdl-36976353
ABSTRACT

INTRODUCTION:

The best first-line treatment for patients with advanced hepatocellular carcinoma (HCC) and Child-Pugh (CP) class B remains unknown. The aim of the present study was to perform a real-world analysis on a large sample of patients with unresectable HCC with CP B treated with atezolizumab plus bevacizumab Vs Lenvatinib.

METHODS:

The study population included patients affected by advanced (BCLC-C) or intermediate (BCLC-B) HCC patients not suitable for locoregional therapies from both the Western and Eastern world (Italy, Germany, Republic of Korea and Japan), who received atezolizumab plus bevacizumab or Lenvatinib as first-line treatment. All the study population presented a CP class of B. The primary endpoint of the study was the overall survival (OS) of CP B patients treated with Lenvatinib compared to atezolizumab plus bevacizumab. Survival curves were estimated using the product-limit method of Kaplan-Meier. The role of stratification factors was analyzed with log-rank tests. Finally, an interaction test was performed for the main baseline clinical characteristics.

RESULTS:

217 CP B HCC patients were enrolled in the study 65 (30%) received atezolizumab plus bevacizumab, and 152 (70%) received lenvatinib. The mOS for patients receiving Lenvatinib was 13.8 months (95% CI 11.6-16.0), compared to 8.2 months (95% CI 6.3-10.2) for patients receiving atezolizumab plus bevacizumab as first-line treatment (atezolizumab plus bevacizumab Vs Lenvatinib HR 1.9, 95% CI 1.2-3.0, p = 0.0050). No statistically significant differences were highlighted in terms of mPFS. The multivariate analysis confirmed that patients receiving Lenvatinib as first-line treatment have a significantly longer OS compared to patients receiving atezolizumab plus bevacizumab (HR 2.01; 95% CI 1.29-3.25, p = 0.0023). By evaluating the cohort of patients who received atezolizumab plus bevacizumab, we found that Child B patients with ECOG PS 0, or BCLC B stage or ALBI grade 1 were those who had benefited from the treatment thus showing survival outcomes no significantly different compared to those receiving Lenvatinib.

CONCLUSION:

The present study suggests for the first time a major benefit from Lenvatinib compared to atezolizumab plus bevacizumab in a large cohort of patients with CP B class HCC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália