Simple tumor profile chart based on cell kinetic parameters and histologic grade is useful for estimating the natural growth rate of hepatocellular carcinoma

被引:25
作者
Nakajima, T [1 ]
Moriguchi, M
Mitsumoto, Y
Katagishi, T
Kimura, H
Shintani, H
Deguchi, T
Okanoue, T
Kagawa, K
Ashihara, T
机构
[1] Kyoto Prefectural Univ Med, Dept Internal Med 3, Kamigyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Pathol 1, Kamigyo Ku, Kyoto 6028566, Japan
[3] Fukuchivama City Hosp, Dept Internal Med, Fukuchivama, Kyoto, Japan
关键词
hepatocellular carcinoma; cell kinetics; growth rate; natural history; apoptosis;
D O I
10.1053/hupa.2002.30194
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Thirty-four untreated hepatocellular carcinomas (HCCs) with known growth rates were classified into 5 groups on a tumor profile chart based on their doubling time (DT), Ki-67-positive index (Ki-67-PI), apoptotic index (Apo-I), and histologic grade. The slow-growing HCCs (DT > 100 days) consisted of well-differentiated tumors with slight cell kinetic imbalance and were divided into groups A and B. Group A had Apo-I values <3%, and most tumors had Ki-67-PI values <10%, whereas group B had Apo-I values of 3parts per thousand to 10parts per thousand and Ki-67-PI values of 10% to 20%. The HCCs with intermediate growth rates, which had Ki-67-PI values similar to those of the tumors in group B, were divided into groups C and D based on differences in cell kinetics: group C consisted of well-differentiated tumors, most of which had Apo-I values <3parts per thousand, and group D consisted of moderately or poorly differentiated tumors with Apo-I values between 10parts per thousand and 20parts per thousand. The rapidly growing tumors (DT < 50 days, group E) had higher Ki-67-PI values than other groups and a wide range of Apo-I values. Rapidly growing tumors were mostly moderately or poorly differentiated, with a large cell kinetic imbalance in favor of cell production. This grouping system is useful for approximating the growth rate of HCCs in a clinical setting, even when only histologic parameters are available. Copyright 2002 (C) by W.B. Saunders Company.
引用
收藏
页码:92 / 99
页数:8
相关论文
共 29 条
[1]   NATURAL-HISTORY OF SMALL UNTREATED HEPATOCELLULAR-CARCINOMA IN CIRRHOSIS - A MULTIVARIATE-ANALYSIS OF PROGNOSTIC FACTORS OF TUMOR-GROWTH RATE AND PATIENT SURVIVAL [J].
BARBARA, L ;
BENZI, G ;
GAIANI, S ;
FUSCONI, F ;
ZIRONI, G ;
SIRINGO, S ;
RIGAMONTI, A ;
BARBARA, C ;
GRIGIONI, W ;
MAZZIOTTI, A ;
BOLONDI, L .
HEPATOLOGY, 1992, 16 (01) :132-137
[2]   MONOCLONAL-ANTIBODIES AGAINST RECOMBINANT PARTS OF THE KI-67 ANTIGEN (MIB-1 AND MIB-3) DETECT PROLIFERATING CELLS IN MICROWAVE-PROCESSED FORMALIN-FIXED PARAFFIN SECTIONS [J].
CATTORETTI, G ;
BECKER, MHG ;
KEY, G ;
DUCHROW, M ;
SCHLUTER, C ;
GALLE, J ;
GERDES, J .
JOURNAL OF PATHOLOGY, 1992, 168 (04) :357-363
[3]  
COLLINS VP, 1956, AMER J ROENTGENOL RA, V76, P988
[4]  
Colombo M, 1998, HEPATO-GASTROENTEROL, V45, P1221
[5]  
COTTER TG, 1990, ANTICANCER RES, V10, P1153
[6]   NATURAL-HISTORY OF MINUTE HEPATOCELLULAR-CARCINOMA SMALLER THAN .3. CENTIMETERS COMPLICATING CIRRHOSIS - A STUDY IN 22 PATIENTS [J].
EBARA, M ;
OHTO, M ;
SHINAGAWA, T ;
SUGIURA, N ;
KIMURA, K ;
MATSUTANI, S ;
MORITA, M ;
SAISHO, H ;
TSUCHIYA, Y ;
OKUDA, K .
GASTROENTEROLOGY, 1986, 90 (02) :289-298
[7]  
Ezaki T, 1996, J SURG ONCOL, V62, P115
[8]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[9]   Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours [J].
Graeber, TG ;
Osmanian, C ;
Jacks, T ;
Housman, DE ;
Koch, CJ ;
Lowe, SW ;
Giaccia, AJ .
NATURE, 1996, 379 (6560) :88-91
[10]   IN-SITU DETECTION OF FRAGMENTED DNA (TUNEL ASSAY) FAILS TO DISCRIMINATE AMONG APOPTOSIS, NECROSIS, AND AUTOLYTIC CELL-DEATH - A CAUTIONARY NOTE [J].
GRASLKRAUPP, B ;
RUTTKAYNEDECKY, B ;
KOUDELKA, H ;
BUKOWSKA, K ;
BURSCH, W ;
SCHULTEHERMANN, R .
HEPATOLOGY, 1995, 21 (05) :1465-1468