Natural history of untreatable hepatocellular carcinoma: A retrospective cohort study

被引:66
作者
Cabibbo, Giuseppe [1 ,2 ]
Maida, Marcello [1 ]
Genco, Chiara [1 ]
Parisi, Pietro [1 ]
Peralta, Marco [1 ]
Antonucci, Michela [1 ,3 ]
Brancatelli, Giuseppe [1 ,4 ]
Camma, Calogero [1 ]
Craxi, Antonio [1 ]
Di Marco, Vito [1 ]
机构
[1] Univ Palermo, Dept Internal Med, Sect Gastroenterol, Piazza Clin 2, I-90127 Palermo, Italy
[2] Univ Palermo, Dept Biopathol & Biomed Methodol, I-90127 Palermo, Italy
[3] Univ Palermo, Dept Oncol, Div Gen Surg & Oncol, I-90127 Palermo, Italy
[4] Univ Palermo, Dept Radiol, DIBIMEF, I-90127 Palermo, Italy
关键词
Hepatocellular carcinoma; Liver; Cancer; Survival; Prognosis; Natural history;
D O I
10.4254/wjh.v4.i9.256
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the clinical course of untreatable hepatocellular carcinoma (HCC) identified at any stage and to identify factors associated with mortality. METHODS: From January 1999 to December 2010, 320 out of 825 consecutive patients with a diagnosis of HCC and not appropriate for curative or palliative treatments were followed and managed with supportive therapy. Cirrhosis was diagnosed by histological or clinical features and liver function was evaluated according to Child-Pugh score. The diagnosis of HCC was performed by Ultra-Sound guided biopsy or by multiphasic contrast-enhanced computed tomography or gadolinium-enhanced magnetic resonance imaging. Data were collected for each patient including all clinical, laboratory and imaging variables necessary for the outcome prediction staging systems considered. HCC staging was performed according Barcelona Clinic Liver Cancer (BCLC) and Cancer of the Liver Italian Program scores. Follow-up time was defined as the number of months from the diagnosis of HCC to death. Prognostic baseline variables were analyzed by multivariate Cox analysis to identify the independent predictors of survival. RESULTS: Seventy-five per cent of patients had hepatitis C. Ascites was present in 169 patients (53%), while hepatic encephalopathy was present in 49 patients (15%). The Child-Pugh score was class A in 105 patients (33%), class B in 142 patients (44%), and class C in 73 patients (23%). One hundred patients (31%) had macroscopic vascular invasion and/or extrahepatic spread of the tumor. A single lesion > 10 cm was observed in 34 patients (11%), while multinodular HCC was present in 189 patients (59%). Thirty nine patients (12%) were BCLC early (A) stage, 55 (17%) were BCLC intermediate (B) stage, 124 (39%) were BCLC advanced (C) stage, and 102 (32%) were end-stage BCLC (D). At the time of this analysis (July 2011), 28 (9%) patients were still alive. Six (2%) patients who were lost during follow-up were censored at the last visit. The overall median survival was 6.8 mo, and the 1-year survival was 32%. The 1-year survival according to BCLC classes was 100%, 79%, 12% and 0%, for BCLC A, B, C and D, respectively. There was a significant difference in survival between each BCLC class. The median survival of patients of BCLC stages A, B, C and D was 33, 17.4, 6.9, and 1.8 mo, respectively (P < 0.05 for comparison between stages). The median survival of Child-Pugh A, B and C classes were 9.8 mo (range 6.4-13), 6.1 (range 4.9-7.3), and 3.7 (range 1.5-6), respectively (P < 0.05 for comparison between stages). By univariate analysis, the variables significantly associated to an increased liklihood of mortality were Eastern Cooperative Oncology Group performance status (PS), presence of ascites, low level of albumin, elevated level of bilirubin, international normalized ratio (INR) and Log-[(alpha fetoprotein (AFP)]. At multivariate analysis, mortality was independently predicted by bad PS (P < 0.0001), high INR values (P = 0.0001) and elevated Log-(AFP) levels (P = 0.009). CONCLUSION: This study confirms the heterogeneous behavior of untreated HCC. BCLC staging remains an important prognostic guide and may be important in decision-making for palliative treatment. (C) 2012 Baishideng. All rights reserved.
引用
收藏
页码:256 / 261
页数:6
相关论文
共 26 条
[11]   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
[12]   ASYMPTOMATIC HEPATOCELLULAR-CARCINOMA IN CHILDS A CIRRHOSIS - A COMPARISON OF NATURAL-HISTORY AND SURGICAL-TREATMENT [J].
COTTONE, M ;
VIRDONE, R ;
FUSCO, G ;
ORLANDO, A ;
TURRI, M ;
CALTAGIRONE, M ;
MARINGHINI, A ;
SCIARRINO, E ;
DEMMA, I ;
NICOLI, N ;
TINE, F ;
SAMMARCO, S ;
PAGLIARO, L .
GASTROENTEROLOGY, 1989, 96 (06) :1566-1571
[13]   CURRENT CONCEPTS Hepatocellular Carcinoma [J].
El-Serag, Hashem B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (12) :1118-1127
[14]   Field-Practice Study of Sorafenib Therapy for Hepatocellular Carcinoma: A Prospective Multicenter Study in Italy [J].
Iavarone, Massimo ;
Cabibbo, Giuseppe ;
Piscaglia, Fabio ;
Zavaglia, Claudio ;
Grieco, Antonio ;
Villa, Erica ;
Camma, Calogero ;
Colombo, Massimo ;
Sangiovanni, Angelo ;
Vavassori, Sara ;
Romeo, Raffaella ;
Di Marco, Vito ;
Craxi, Antonio ;
Borghi, Alberto ;
Granito, Alessandro ;
Bolondi, Luigi ;
Airoldi, Aldo ;
Pinzello, Giovambattista ;
Biolato, Marco ;
Racco, Simona ;
Pompili, Maurizio ;
Lei, Barbara ;
De Maria, Nicola .
HEPATOLOGY, 2011, 54 (06) :2055-2063
[15]   Seeding after radiofrequency ablation of hepatocellular carcinoma in patients with cirrhosis:: A prospective study [J].
Latteri, F. ;
Sandonato, L. ;
Di Marco, V. ;
Parisi, P. ;
Cabibbo, G. ;
Lombardo, G. ;
Galia, M. ;
Midiri, M. ;
Latteri, M. A. ;
Craxi, A. .
DIGESTIVE AND LIVER DISEASE, 2008, 40 (08) :684-689
[16]   Prognosis of hepatocellular carcinoma:: The BCLC staging classification [J].
Llovet, JM ;
Brú, C ;
Bruix, J .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :329-338
[17]   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
[18]   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
[19]   TOXICITY AND RESPONSE CRITERIA OF THE EASTERN-COOPERATIVE-ONCOLOGY-GROUP [J].
OKEN, MM ;
CREECH, RH ;
TORMEY, DC ;
HORTON, J ;
DAVIS, TE ;
MCFADDEN, ET ;
CARBONE, PP .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1982, 5 (06) :649-655
[20]   Prognostic factors in patients with advanced hepatocellular carcinoma treated with sorafenib [J].
Pinter, M. ;
Sieghart, W. ;
Hucke, F. ;
Graziadei, I. ;
Vogel, W. ;
Maieron, A. ;
Koenigsberg, R. ;
Weissmann, A. ;
Kornek, G. ;
Matejka, J. ;
Stauber, R. ;
Buder, R. ;
Gruenberger, B. ;
Schoeniger-Hekele, M. ;
Mueller, C. ;
Peck-Radosavljevic, M. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2011, 34 (08) :949-959