Impact of branched-chain amino acid supplementation on survival in patients with advanced hepatocellular carcinoma treated with sorafenib: A multicenter retrospective cohort study

Aim The therapeutic efficacy of branched‐chain amino acid (BCAA) when added to sorafenib has not been fully assessed in patients with advanced hepatocellular carcinoma (HCC). This multicenter study investigated whether BCAA supplementation improves prognosis in patients with advanced HCC who underwe...

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Veröffentlicht in:Hepatology research 2016-09, Vol.46 (10), p.1002-1010
Hauptverfasser: Imanaka, Kazuho, Ohkawa, Kazuyoshi, Tatsumi, Tomohide, Katayama, Kazuhiro, Inoue, Atsuo, Imai, Yasuharu, Oshita, Masahide, Iio, Sadaharu, Mita, Eiji, Fukui, Hiroyuki, Yamada, Akira, Nakanishi, Fumihiko, Inada, Masami, Doi, Yoshinori, Suzuki, Kunio, Kaneko, Akira, Marubashi, Shigeru, Ito, Yuri, Fukui, Keisuke, Sakamori, Ryotaro, Yakushijin, Takayuki, Hiramatsu, Naoki, Hayashi, Norio, Takehara, Tetsuo
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Sprache:eng
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Zusammenfassung:Aim The therapeutic efficacy of branched‐chain amino acid (BCAA) when added to sorafenib has not been fully assessed in patients with advanced hepatocellular carcinoma (HCC). This multicenter study investigated whether BCAA supplementation improves prognosis in patients with advanced HCC who underwent sorafenib treatment. Methods This retrospective analysis included 256 patients with advanced HCC treated with sorafenib, including 55 who did and 201 who did not receive BCAA supplementation. Clinical characteristics and outcomes in relation to Child–Pugh classification were compared in the two groups. Statistical analyses of univariate, multivariate and propensity score‐based procedures were used for this study. Results Assessment of 216 Child–Pugh A patients showed that median overall survival was significantly longer in patients with BCAA supplementation than in those without it (440 vs 299 days, P = 0.023). Multivariate analysis showed that BCAA supplementation (P = 0.023), low α‐fetoprotein (
ISSN:1386-6346
1872-034X
DOI:10.1111/hepr.12640