Skeletal Muscle Loss during Tyrosine Kinase Inhibitor Treatment for Advanced Hepatocellular Carcinoma Patients

被引:33
作者
Uchikawa, Shinsuke [1 ]
Kawaoka, Tomokazu [1 ]
Namba, Maiko [1 ]
Kodama, Kenichiro [1 ]
Ohya, Kazuki [1 ]
Morio, Kei [1 ]
Nakahara, Takashi [1 ]
Murakami, Eisuke [1 ]
Tsuge, Masataka [1 ]
Hiramatsu, Akira [1 ]
Imamura, Michio [1 ]
Takahashi, Shoichi [1 ]
Chayama, Kazuaki [1 ]
Aikata, Hiroshi [1 ]
机构
[1] Hiroshima Univ, Dept Gastroenterol & Metab, Inst Biomed & Hlth Sci, Appl Life Sci, Hiroshima, Japan
关键词
Skeletal muscle; Hepatocellular carcinoma; Tyrosine kinase inhibitor; Sorafenib; Lenvatinib; SORAFENIB; SARCOPENIA; DEPLETION; CARNITINE; OBESITY; GROWTH; MASS; FAT;
D O I
10.1159/000503829
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The measurement of body composition such as the skeletal muscle index (SMI) has been reported to be useful for predicting prognosis in hepatocellular carcinoma (HCC). In this study, we analyzed skeletal muscle change during sorafenib and lenvatinib therapy and the association between SMI and prognosis. Methods: A total of 67 patients with advanced HCC and Child-Pugh grade A status treated with tyrosine kinase inhibitors (TKIs) at Hiroshima University between September 2009 and December 2018 were enrolled in this retrospective cohort study. Patients underwent computed tomography (CT) imaging before starting sorafenib treatment and 1-3 months after treatment initiation. Results: In all patients, the median SMI was 45.3 cm(2)/m(2) before TKI treatment and 42.1 cm(2)/m(2) after treatment; 54 of 67 (80.6%) patients experienced SMI loss. The median Delta SMI was -1.5 cm(2)/m(2)/months, and no difference in Delta SMI was observed between patients receiving sorafenib and lenvatinib. No significant differences were observed in median Delta SMI between patients with and without progressive disease (-2.35 and -1.1 cm(2)/m(2)/months, respectively), albumin-bilirubin grade 1 and 2 group disease (-1.7 and -1.5 cm(2)/m(2)/months, respectively), and relative dose intensity <= 80 and >80 (-1.8 and -1.2 cm(2)/m(2)/months, respectively). Conclusion: This report demonstrated that patients receiving TKI treatment experienced a significant loss of skeletal muscle mass regardless of disease progression, hepatic reserve, or which TKI (sorafenib or lenvatinib) they received.
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收藏
页码:148 / 155
页数:8
相关论文
共 27 条
[1]   Association of Skeletal Muscle Wasting With Treatment With Sorafenib in Patients With Advanced Renal Cell Carcinoma: Results From a Placebo-Controlled Study [J].
Antoun, Sami ;
Birdsell, Laura ;
Sawyer, Michael B. ;
Venner, Peter ;
Escudier, Bernard ;
Baracos, Vickie E. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (06) :1054-1060
[2]   Fibroblast growth factor 19 regulates skeletal muscle mass and ameliorates muscle wasting in mice [J].
Benoit, Berengere ;
Meugnier, Emmanuelle ;
Castelli, Martina ;
Chanon, Stephanie ;
Vieille-Marchiset, Aurelie ;
Durand, Christine ;
Bendridi, Nadia ;
Pesenti, Sandra ;
Monternier, Pierre-Axel ;
Durieux, Anne-Cecile ;
Freyssenet, Damien ;
Rieusset, Jennifer ;
Lefai, Etienne ;
Vidal, Hubert ;
Ruzzin, Jerome .
NATURE MEDICINE, 2017, 23 (08) :990-+
[3]   Autophagy and Mitophagy in Cardiovascular Disease [J].
Bravo-San Pedro, Jose Manuel ;
Kroemer, Guido ;
Galluzzi, Lorenzo .
CIRCULATION RESEARCH, 2017, 120 (11) :1812-1824
[4]   Hepatocellular carcinoma: clinical frontiers and perspectives [J].
Bruix, Jordi ;
Gores, Gregory J. ;
Mazzaferro, Vincenzo .
GUT, 2014, 63 (05) :844-855
[5]   Sorafenib (BAY 43-9006) inhibits tumor growth and vascularization and induces tumor apoptosis and hypoxia in RCC xenograft models [J].
Chang, Yong S. ;
Adnane, Jalila ;
Trail, Pamela A. ;
Levy, Joan ;
Henderson, Arris ;
Xue, Dahai ;
Bortolon, Elizabeth ;
Ichetovkin, Marina ;
Chen, Charles ;
McNabola, Angela ;
Wilkie, Dean ;
Carter, Christopher A. ;
Taylor, Ian C. A. ;
Lynch, Mark ;
Wilhelm, Scott .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2007, 59 (05) :561-574
[6]   Sorafenib Alone versus Sorafenib Combined with Transarterial Chemoembolization for Advanced-Stage Hepatocellular Carcinoma: Results of Propensity Score Analyses [J].
Choi, Gwang Hyeon ;
Shim, Ju Hyun ;
Kim, Min-Joo ;
Ryu, Min-Hee ;
Ryoo, Baek-Yeol ;
Kang, Yoon-Koo ;
Shin, Yong Moon ;
Kim, Kang Mo ;
Lim, Young-Suk ;
Lee, Han Chu .
RADIOLOGY, 2013, 269 (02) :602-610
[7]   Cause and management of muscle wasting in chronic liver disease [J].
Dasarathy, Srinivasan .
CURRENT OPINION IN GASTROENTEROLOGY, 2016, 32 (03) :159-165
[8]   Coordinate activation of Shh and PI3K signaling in PTEN-deficient glioblastoma: new therapeutic opportunities [J].
Filbin, Mariella Gruber ;
Dabral, Sukriti K. ;
Pazyra-Murphy, Maria F. ;
Ramkissoon, Shakti ;
Kung, Andrew L. ;
Pak, Ekaterina ;
Chung, Jarom ;
Theisen, Matthew A. ;
Sun, Yanping ;
Franchetti, Yoko ;
Sun, Yu ;
Shulman, David S. ;
Redjal, Navid ;
Tabak, Barbara ;
Beroukhim, Rameen ;
Wang, Qi ;
Zhao, Jean ;
Dorsch, Marion ;
Buonamici, Silvia ;
Ligon, Keith L. ;
Kelleher, Joseph F. ;
Segal, Rosalind A. .
NATURE MEDICINE, 2013, 19 (11) :1518-+
[9]   Sarcopenia, intramuscular fat deposition, and visceral adiposity independently predict the outcomes of hepatocellular carcinoma [J].
Fujiwara, Naoto ;
Nakagawa, Hayato ;
Kudo, Yotaro ;
Tateishi, Ryosuke ;
Taguri, Masataka ;
Watadani, Takeyuki ;
Nakagomi, Ryo ;
Kondo, Mayuko ;
Nakatsuka, Takuma ;
Minami, Tatsuya ;
Sato, Masaya ;
Uchino, Koji ;
Enooku, Kenichiro ;
Kondo, Yuji ;
Asaoka, Yoshinari ;
Tanaka, Yasuo ;
Ohtomo, Kuni ;
Shiina, Shuichiro ;
Koike, Kazuhiko .
JOURNAL OF HEPATOLOGY, 2015, 63 (01) :131-140
[10]   Muscle volume loss as a prognostic marker in hepatocellular carcinoma patients treated with sorafenib [J].
Hiraoka, Atsushi ;
Hirooka, Masashi ;
Koizumi, Yohei ;
Izumoto, Hirofumi ;
Ueki, Hidetaro ;
Kaneto, Miho ;
Kitahata, Shogo ;
Aibiki, Toshihiko ;
Tomida, Hideomi ;
Miyamoto, Yuji ;
Yamago, Hiroka ;
Suga, Yoshifumi ;
Iwasaki, Ryuichiro ;
Mori, Kenichiro ;
Miyata, Hideki ;
Tsubouchi, Eiji ;
Kishida, Masato ;
Ninomiya, Tomoyuki ;
Abe, Masanori ;
Matsuura, Bunzo ;
Kawasaki, Hideki ;
Hiasa, Yoichi ;
Michitaka, Kojiro .
HEPATOLOGY RESEARCH, 2017, 47 (06) :558-565