BMC Cancer (Jun 2018)

Hepatic arterial infusion chemotherapy followed by sorafenib in patients with advanced hepatocellular carcinoma (HICS 55): an open label, non-comparative, phase II trial

  • Masahiro Hatooka,
  • Tomokazu Kawaoka,
  • Hiroshi Aikata,
  • Yuki Inagaki,
  • Kei Morio,
  • Takashi Nakahara,
  • Eisuke Murakami,
  • Masataka Tsuge,
  • Akira Hiramatsu,
  • Michio Imamura,
  • Yoshiiku Kawakami,
  • Kazuo Awai,
  • Keiichi Masaki,
  • Koji Waki,
  • Hirotaka Kohno,
  • Hiroshi Kohno,
  • Takashi Moriya,
  • Yuko Nagaoki,
  • Toru Tamura,
  • Hajime Amano,
  • Yoshio Katamura,
  • Kazuaki Chayama

DOI
https://doi.org/10.1186/s12885-018-4519-y
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 10

Abstract

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Abstract 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 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 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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