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Survival Benefit of Hepatic Arterial Infusion Chemotherapy over Sorafenib in the Treatment of Locally Progressed Hepatocellular Carcinoma.
Iwamoto, Hideki; Niizeki, Takashi; Nagamatsu, Hiroaki; Ueshima, Kazuomi; Nomura, Takako; Kuzuya, Teiji; Kasai, Kazuhiro; Kooka, Yohei; Hiraoka, Atsushi; Sugimoto, Rie; Yonezawa, Takehiro; Ishihara, Akio; Deguchi, Akihiro; Arai, Hirotaka; Shimose, Shigeo; Shirono, Tomotake; Nakano, Masahito; Okamura, Shusuke; Noda, Yu; Kamachi, Naoki; Sakai, Miwa; Suzuki, Hiroyuki; Aino, Hajime; Matsukuma, Norito; Matsugaki, Satoru; Ogata, Kei; Yano, Yoichi; Ueno, Takato; Kajiwara, Masahiko; Itano, Satoshi; Fukuizumi, Kunitaka; Kawano, Hiroshi; Noguchi, Kazunori; Tanaka, Masatoshi; Yamaguchi, Taizo; Kuromatsu, Ryoko; Kawaguchi, Atsushi; Koga, Hironori; Torimura, Takuji.
Afiliação
  • Iwamoto H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Niizeki T; Iwamoto Internal Medicine Clinic, Kitakyusyu 802-0832, Japan.
  • Nagamatsu H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Ueshima K; Department of Gastroenterology, Juntendo University, Bunkyo-ku 113-8421, Japan.
  • Nomura T; Department of Gastroenterology and Hepatology, Faculty of Medicine, Kindai University, Osaka 589-8511, Japan.
  • Kuzuya T; Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Miki 761-0793, Japan.
  • Kasai K; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan.
  • Kooka Y; Division of Gastroenterology, IMS Sapporo Digestive Disease Center General Hospital, Sapporo 063-0842, Japan.
  • Hiraoka A; Division of Hepatology, Department of Internal Medicine, Iwate Medical University School of Medicine, Iwate 028-3695, Japan.
  • Sugimoto R; Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama 790-0024, Japan.
  • Yonezawa T; Department of Hepato-Biliary-Pancreatology, National Hospital Organization Kyushu Cancer Center, Fukuoka 811-1395, Japan.
  • Ishihara A; Department of Gastroenterology, Hachinohe Red Cross Hospital, Aomori 039-1104, Japan.
  • Deguchi A; Department of Gastroenterology, Osaka National Hospital, Osaka 540-0006, Japan.
  • Arai H; Department of Gastroenterology, Kagawa Rosai Hospital, Marugame 763-8502, Japan.
  • Shimose S; Department of Gastroenterology, Maebashi Red Cross Hospital, Maebashi 371-0811, Japan.
  • Shirono T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Nakano M; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Okamura S; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Noda Y; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Kamachi N; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Sakai M; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Suzuki H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Aino H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Matsukuma N; Division of Gastroenterology, Department of Medicine, Social Insurance Tagawa Hospital, Tagawa 826-0023, Japan.
  • Matsugaki S; Department of Gastroenterology, Kurume General Hospital, Kurume 830-8521, Japan.
  • Ogata K; Department of Gastroenterology, Tobata Kyoritsu Hospital, Kitakyusyu 804-0093, Japan.
  • Yano Y; Department of Gastroenterology, Kurume University Medical Center, Kurume 839-0863, Japan.
  • Ueno T; Department of Gastroenterology, Saga Central Hospital, Saga 849-8522, Japan.
  • Kajiwara M; Department of Gastroenterology, Asakura Medical Association Hospital, Asakura 838-0069, Japan.
  • Itano S; Department of Gastroenterology, Chikugo City Hospital, Chikugo 833-0041, Japan.
  • Fukuizumi K; Department of Gastroenterology, Kurume Central Hospital, Kurume 830-0001, Japan.
  • Kawano H; Department of Gastroenterology, National Hospital Organization Kyushu Medical Center, Fukuoka 810-8563, Japan.
  • Noguchi K; Department of Gastroenterology, St. Mary's Hospital, Kurume 830-8543, Japan.
  • Tanaka M; Department of Gastroenterology, Omuta City Hospital, Omuta 836-0861, Japan.
  • Yamaguchi T; Department of Gastroenterology, Yokokura Hospital, Miyama 839-0215, Japan.
  • Kuromatsu R; Iwamoto Internal Medicine Clinic, Kitakyusyu 802-0832, Japan.
  • Kawaguchi A; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • Koga H; Center for Comprehensive Community Medicine Faculty of Medicine, Saga University, Saga 840-0027, Japan.
  • Torimura T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
  • New Fp Study Group; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan.
Cancers (Basel) ; 13(4)2021 Feb 05.
Article em En | MEDLINE | ID: mdl-33562793
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article