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Evolution of Survival Impact of Molecular Target Agents in Patients with Advanced Hepatocellular Carcinoma.
Kobayashi, Kazufumi; Ogasawara, Sadahisa; Takahashi, Aya; Seko, Yuya; Unozawa, Hidemi; Sato, Rui; Watanabe, Shunji; Moriguchi, Michihisa; Morimoto, Naoki; Tsuchiya, Satoshi; Iwai, Kenji; Inoue, Masanori; Ogawa, Keita; Ishino, Takamasa; Iwanaga, Terunao; Sakuma, Takafumi; Fujita, Naoto; Kanzaki, Hiroaki; Koroki, Keisuke; Nakamura, Masato; Kanogawa, Naoya; Kiyono, Soichiro; Kondo, Takayuki; Saito, Tomoko; Nakagawa, Ryo; Suzuki, Eiichiro; Ooka, Yoshihiko; Nakamoto, Shingo; Tawada, Akinobu; Chiba, Tetsuhiro; Arai, Makoto; Kanda, Tatsuo; Maruyama, Hitoshi; Nagashima, Kengo; Kato, Jun; Isoda, Norio; Aramaki, Takeshi; Itoh, Yoshito; Kato, Naoya.
Afiliación
  • Kobayashi K; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Ogasawara S; Translational Research and Development Center, Chiba University Hospital, Chiba, Japan.
  • Takahashi A; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Seko Y; Translational Research and Development Center, Chiba University Hospital, Chiba, Japan.
  • Unozawa H; Department of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Sato R; Department of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Watanabe S; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Moriguchi M; Division of Interventional Radiology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Morimoto N; Division of Gastroenterology, Department of Medicine, Jichi Medical University, Tochigi, Japan.
  • Tsuchiya S; Department of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Iwai K; Division of Gastroenterology, Department of Medicine, Jichi Medical University, Tochigi, Japan.
  • Inoue M; Division of Interventional Radiology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Ogawa K; Division of Interventional Radiology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Ishino T; Numazu City Hospital, Shizuoka, Japan.
  • Iwanaga T; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Sakuma T; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Fujita N; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kanzaki H; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Koroki K; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Nakamura M; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kanogawa N; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kiyono S; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kondo T; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Saito T; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Nakagawa R; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Suzuki E; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Ooka Y; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Nakamoto S; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Tawada A; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Chiba T; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Arai M; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kanda T; Department of Medical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Maruyama H; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Nagashima K; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kato J; Department of Medical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Isoda N; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Aramaki T; Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
  • Itoh Y; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Kato N; Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.
Liver Cancer ; 11(1): 48-60, 2022 Jan.
Article en En | MEDLINE | ID: mdl-35222507
BACKGROUND AND AIMS: The prognosis of patients with advanced hepatocellular carcinoma (HCC) is expected to improve as multiple molecular target agents (MTAs) are now available. However, the impact of the availability of sequential MTAs has not been fully verified yet. APPROACH AND RESULTS: We retrospectively collected the data on the whole clinical course of 877 patients who received any MTAs as first-line systemic therapy for advanced HCC between June 2009 and March 2019. The study population was divided into 3 groups according to the date of first-line MTA administration (period 1: 2009-2012, n = 267; period 2: 2013-2016, n = 352; period 3: 2017-2019, n = 258). Then, we compared the number of MTAs used, overall survival (OS), and MTA treatment duration among the 3 groups. Analysis was also performed separately for advanced-stage and nonadvanced-stage HCC. The proportion of patients who received multiple MTAs was remarkably increased over time (1.1%, 10.2%, and 42.6% in periods 1, 2, and 3, respectively, p < 0.001). The median OS times were prolonged to 10.4, 11.3, and 15.2 months in periods 1, 2, and 3, respectively (p = 0.016). Similarly, the MTA treatment durations were extended (2.7, 3.2, and 6.6 months in periods 1, 2, and 3, respectively; p < 0.001). We confirmed that the correlation between OS and MTA treatment duration was strengthened (period 1: 0.395, period 2: 0.505, and period 3: 0.667). All these trends were pronounced in the patients with advanced-stage HCC but limited in the patients with nonadvanced-stage HCC. CONCLUSIONS: The availability of multiple MTAs had steadily improved the prognosis of patients with advanced HCC patients, particularly advanced-stage HCC patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Liver Cancer Año: 2022 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Liver Cancer Año: 2022 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Suiza