Comparison of systems for assessment of post-therapeutic response to sorafenib for hepatocellular carcinoma

被引:34
作者
Arizumi, Tadaaki [1 ]
Ueshima, Kazuomi [1 ]
Takeda, Haruhiko [2 ]
Osaki, Yukio [2 ]
Takita, Masahiro [1 ]
Inoue, Tatsuo [1 ]
Kitai, Satoshi [1 ]
Yada, Norihisa [1 ]
Hagiwara, Satoru [1 ]
Minami, Yasunori [1 ]
Sakurai, Toshiharu [1 ]
Nishida, Naoshi [1 ]
Kudo, Masatoshi [1 ]
机构
[1] Kinki Univ, Fac Med, Dept Gastroenterol & Hepatol, Osakasayama, Osaka 5898511, Japan
[2] Osaka Red Cross Hosp, Dept Gastroenterol & Hepatol, Tennoji Ku, Osaka 5438555, Japan
关键词
Hypervascular lesion; Liver cirrhosis; Response evaluation criteria in solid tumors; Response evaluation criteria in cancer of the liver; Tumor viability; INHIBITOR;
D O I
10.1007/s00535-014-0936-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To test the hypothesis that use of the response evaluation criteria in cancer of the liver (RECICL), an improved evaluation system designed to address the limitations of the response evaluation criteria in solid tumors 1.1 (RECIST1.1) and modified RECIST (mRECIST), provides for more accurate evaluation of response of patients with hepatocellular carcinoma (HCC) to treatment with sorafenib, a molecularly targeted agent, as assessed by overall survival (OS). The therapeutic response of 156 patients with advanced HCC who had been treated with sorafenib therapy for more than 1 month was evaluated using the RECIST1.1, mRECIST, and RECICL. After categorization as showing progressive disease (PD), stable disease (SD), or objective response, the association between OS and categorization was examined using the Kaplan-Meier method to develop survival curves. The 141 cases categorized as PD or SD by the RECIST1.1, but objective response by the mRECIST and RECICL, were further analyzed for determination of the association between OS and categorization. Only categorization using the RECICL was found to be significantly correlated with OS (p = 0.0033). Among the patients categorized as SD or PD by the RECIST1.1, reclassification by the RECICL but not the mRECIST was found to be significantly associated with OS and allowed for precise prediction of prognosis (p = 0.0066). Only the use of the RECICL allowed for identification of a subgroup of HCC patients treated with sorafenib with improved prognosis. The RECICL should, therefore, be considered a superior system for assessment of therapeutic response.
引用
收藏
页码:1578 / 1587
页数:10
相关论文
共 16 条
[1]  
[Anonymous], GEN RUL CLIN PATH ST
[2]   Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial [J].
Cheng, Ann-Lii ;
Kang, Yoon-Koo ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Luo, Rongcheng ;
Feng, Jifeng ;
Ye, Shenglong ;
Yang, Tsai-Sheng ;
Xu, Jianming ;
Sun, Yan ;
Liang, Houjie ;
Liu, Jiwei ;
Wang, Jiejun ;
Tak, Won Young ;
Pan, Hongming ;
Burock, Karin ;
Zou, Jessie ;
Voliotis, Dimitris ;
Guan, Zhongzhen .
LANCET ONCOLOGY, 2009, 10 (01) :25-34
[3]   Evaluation of responses to chemoembolization in patients with unresectable hepatocellular carcinoma [J].
Ebied, OM ;
Federle, MP ;
Carr, BI ;
Pealer, KM ;
Li, W ;
Amesur, N ;
Zajko, A .
CANCER, 2003, 97 (04) :1042-1050
[4]   Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis [J].
El-Serag, Hashem B. ;
Rudolph, Lenhard .
GASTROENTEROLOGY, 2007, 132 (07) :2557-2576
[5]   Comparison of the effects of the kinase inhibitors imatinib, sorafenib, and transforming growth factor-β receptor inhibitor on extravasation of nanoparticles from neovasculature [J].
Kano, Mitsunobu R. ;
Komuta, Yukari ;
Iwata, Caname ;
Oka, Masako ;
Shirai, Yo-taro ;
Morishita, Yasuyuki ;
Ouchi, Yasuyoshi ;
Kataoka, Kazunori ;
Miyazono, Kohei .
CANCER SCIENCE, 2009, 100 (01) :173-180
[6]   Modified RECIST (mRECIST) Assessment for Hepatocellular Carcinoma [J].
Lencioni, Riccardo ;
Llovet, Josep M. .
SEMINARS IN LIVER DISEASE, 2010, 30 (01) :52-60
[7]   Molecular targeted therapies in hepatocellular carcinoma [J].
Llovet, Josep M. ;
Bruix, Jordi .
HEPATOLOGY, 2008, 48 (04) :1312-1327
[8]   Sorafenib in advanced hepatocellular carcinoma [J].
Llovet, Josep M. ;
Ricci, Sergio ;
Mazzaferro, Vincenzo ;
Hilgard, Philip ;
Gane, Edward ;
Blanc, Jean-Frederic ;
Cosme de Oliveira, Andre ;
Santoro, Armando ;
Raoul, Jean-Luc ;
Forner, Alejandro ;
Schwartz, Myron ;
Porta, Camillo ;
Zeuzem, Stefan ;
Bolondi, Luigi ;
Greten, Tim F. ;
Galle, Peter R. ;
Seitz, Jean-Francois ;
Borbath, Ivan ;
Haussinger, Dieter ;
Giannaris, Tom ;
Shan, Minghua ;
Moscovici, Marius ;
Voliotis, Dimitris ;
Bruix, Jordi .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (04) :378-390
[9]   Design and endpoints of clinical trials in hepatocellular carcinoma [J].
Llovet, Josep M. ;
Di Bisceglie, Adrian M. ;
Bruix, Jordi ;
Kramer, Barnett S. ;
Lencioni, Riccardo ;
Zhu, Andrew X. ;
Sherman, Morris ;
Schwartz, Myron ;
Lotze, Michael ;
Talwalkar, Jayant ;
Gores, Gregory J. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (10) :698-711
[10]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO