Cancers (Feb 2021)

Survival Benefit of Hepatic Arterial Infusion Chemotherapy over Sorafenib in the Treatment of Locally Progressed Hepatocellular Carcinoma

  • Hideki Iwamoto,
  • Takashi Niizeki,
  • Hiroaki Nagamatsu,
  • Kazuomi Ueshima,
  • Takako Nomura,
  • Teiji Kuzuya,
  • Kazuhiro Kasai,
  • Yohei Kooka,
  • Atsushi Hiraoka,
  • Rie Sugimoto,
  • Takehiro Yonezawa,
  • Akio Ishihara,
  • Akihiro Deguchi,
  • Hirotaka Arai,
  • Shigeo Shimose,
  • Tomotake Shirono,
  • Masahito Nakano,
  • Shusuke Okamura,
  • Yu Noda,
  • Naoki Kamachi,
  • Miwa Sakai,
  • Hiroyuki Suzuki,
  • Hajime Aino,
  • Norito Matsukuma,
  • Satoru Matsugaki,
  • Kei Ogata,
  • Yoichi Yano,
  • Takato Ueno,
  • Masahiko Kajiwara,
  • Satoshi Itano,
  • Kunitaka Fukuizumi,
  • Hiroshi Kawano,
  • Kazunori Noguchi,
  • Masatoshi Tanaka,
  • Taizo Yamaguchi,
  • Ryoko Kuromatsu,
  • Atsushi Kawaguchi,
  • Hironori Koga,
  • Takuji Torimura,
  • New FP Study Group,
  • Kurume Liver Cancer Study Group of Japan

DOI
https://doi.org/10.3390/cancers13040646
Journal volume & issue
Vol. 13, no. 4
p. 646

Abstract

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BACKROUND: Not all patients with hepatocellular carcinoma (HCC) benefit from treatment with molecular targeted agents such as sorafenib. We investigated whether New-FP (fine-powder cisplatin and 5-fluorouracil), a hepatic arterial infusion chemotherapy regimen, is more favorable than sorafenib as an initial treatment for locally progressed HCC. METHODS: To avoid selection bias, we corrected the data from different facilities that did or did not perform New-FP therapy. In total, 1709 consecutive patients with HCC initially treated with New-FP or sorafenib; 1624 (New-FP, n = 644; sorafenib n = 980) were assessed. After propensity score matching (PSM), overall survival (OS) and prognostic factors were assessed (n = 344 each). Additionally, the patients were categorized into four groups: cohort-1 [(without macrovascular invasion (MVI) and extrahepatic spread (EHS)], cohort-2 (with MVI), cohort-3 (with EHS), and cohort-4 (with MVI and EHS) to clarify the efficacy of each treatment. RESULTS: New-FP prolonged OS than sorafenib after PSM (New-FP, 12 months; sorafenib, 7.9 months; p < 0.001). Sorafenib treatment, and severe MVI and EHS were poor prognostic factors. In the subgroup analyses, the OS was significantly longer the New-FP group in cohort-2. CONCLUSIONS: Local treatment using New-FP is a potentially superior initial treatment compared with sorafenib as a multidisciplinary treatment in locally progressed HCC without EHS.

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