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Hepatic arterial infusion chemotherapy followed by sorafenib in patients with advanced hepatocellular carcinoma (HICS 55): an open label, non-comparative, phase II trial.
Hatooka, Masahiro; Kawaoka, Tomokazu; Aikata, Hiroshi; Inagaki, Yuki; Morio, Kei; Nakahara, Takashi; Murakami, Eisuke; Tsuge, Masataka; Hiramatsu, Akira; Imamura, Michio; Kawakami, Yoshiiku; Awai, Kazuo; Masaki, Keiichi; Waki, Koji; Kohno, Hirotaka; Kohno, Hiroshi; Moriya, Takashi; Nagaoki, Yuko; Tamura, Toru; Amano, Hajime; Katamura, Yoshio; Chayama, Kazuaki.
Afiliação
  • Hatooka M; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Kawaoka T; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Aikata H; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan. aikata@hiroshima-u.ac.jp.
  • Inagaki Y; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Morio K; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Nakahara T; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Murakami E; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Tsuge M; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Hiramatsu A; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Imamura M; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Kawakami Y; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
  • Awai K; Department of Diagnostic Radiology, Graduate School of Biomedical Sciences, Hiroshima, 734-8551, Japan.
  • Masaki K; Hiroshima City Asa Hospital, Hiroshima, Japan.
  • Waki K; Hiroshima City Asa Hospital, Hiroshima, Japan.
  • Kohno H; Kure Medical Center, Hiroshima, Japan.
  • Kohno H; Kure Medical Center, Hiroshima, Japan.
  • Moriya T; Chugoku Rousai Hospital, Hiroshima, Japan.
  • Nagaoki Y; Mazda Hospital, Hiroshima, Japan.
  • Tamura T; Mazda Hospital, Hiroshima, Japan.
  • Amano H; Onomichi General Hospital, Hiroshima, Japan.
  • Katamura Y; Onomichi General Hospital, Hiroshima, Japan.
  • Chayama K; Department of Gastroenterology and Metabolism, Institute of Biomedical & Health Science, Hiroshima University, Hiroshima, 734-8551, Japan.
BMC Cancer ; 18(1): 633, 2018 Jun 04.
Article em En | MEDLINE | ID: mdl-29866075
BACKGROUND: In patients with advanced hepatocellular carcinoma (HCC), evidence is unclear as to whether hepatic arterial infusion chemotherapy (HAIC) or sorafenib is superior. We performed a prospective, open-label, non-comparative phase II study to assess survival with HAIC or HAIC converted to sorafenib. METHODS: Fifty-five patients were prospectively enrolled. Patients received HAIC as a second course if they had complete response, partial response, or stable disease (SD) with an alpha fetoprotein (AFP) ratio < 1 or a des-γ-carboxy prothrombin (DCP) ratio < 1. Patients were switched to sorafenib if they had SD with an AFP ratio > 1 and a DCP ratio > 1 or disease progression. The primary endpoint was the 1-year survival rate. Secondary endpoints were the 2-year survival rate, HAIC response, survival rate among HAIC responders, progression-free survival, and adverse events. RESULTS: Of the 55 patients in the intent-to-treat population, the 1-year and 2-year survival rates were 64.0 and 48.3%, respectively. After the first course of HAIC, one (1.8%) patient showed complete response, 13 (23.6%) showed partial response, 30 (54.5%) had SD, and 10 (18.1%) patients had progressive disease. Twenty-three patients (41.8%) had SD with AFP ratios < 1 or DCP ratios < 1, and 7 (12.7%) had SD with AFP ratios > 1 and DCP ratios > 1. Thirty-seven patients (68.5%) were responders and 17 (30.9%) were non-responders to HAIC. In responders, the 1-year and 2-year survival rates were 78 and 62%, respectively. CONCLUSION: Given the results of this study, this protocol deserves consideration for patients with advanced HCC. This trial was registered prospectively from December 12. 2012 to September 1. 2016.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infusões Intra-Arteriais / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Hepatocelular / Sorafenibe / Neoplasias Hepáticas Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infusões Intra-Arteriais / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Hepatocelular / Sorafenibe / Neoplasias Hepáticas Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão