{"title":"单克隆抗体Ki-67作为肝细胞癌预后因素的价值","authors":"Jiro Yoshimoto, Toyohito Iwata, Shigeru Takamori, Kuniaki Kojima, Shunji Futagawa","doi":"10.1016/S0928-4346(96)00345-3","DOIUrl":null,"url":null,"abstract":"<div><p>We studied the proliferative activity of hepatocellular carcinoma (HCC) by immunohistochemical staining with Ki-67, a monoclonal antibody to nuclear protein observed in the proliferative period of the cell cycle, and evaluated the usefulness of Ki-67 as a prognostic factor. Of the patients who underwent hepatectomy for HCC at our department, 56 cases in which pathological studies for the tumor showed no degeneration or necrosis were selected. Immunohistochemical staining was performed according to the method of Shi et al., using MIB-1 monoclonal antibody (Immunotech, SA) as a primary antibody. Ki-67 L.I. was significantly higher in chronic hepatitis (CH) and liver cirrhosis (LC) than in normal liver, and the L.I. was also significantly higher in non-cancerous tissue of the patients with HCC than in tissues with other liver diseases. In patients with a history of portal hypertension, the L.I. in non-cancerous liver tissue was significantly lower at the previous operation for portal hypertension without HCC than that at the subsequent operation for HCC. The L.I. was significantly higher in patients who showed a high serum AFP level and in those who had intrahepatic metastasis. It also tended to be higher in patients with vessel invasion, infiltration to capsule, aneuploidy tumor cells, and poor differentiation. The cumulative survival rate was significantly lower in patients with the L.I. of 10% or higher than in those with the L.I. of less than 10% in cancerous region. Recurrence was observed earlier after hepatectomy in patients with higher L.I. and the L.I. was significantly higher in those who had recurrence within 12 months. In the patients who could be followed up, the L.I. was significantly higher in those who had multiple recurrence after hepatectomy than in those who had single-lesion recurrence. The incidence of HCC was higher in patients with CH or LC in which the proliferative activity was abnormally enhanced for a prolonged period, suggesting that hepatocyte hyperproliferation triggers hepatic carcinogenesis. In addition, long-term survival was expected even in patients with advanced HCC if the L.I. in preoperative biopsy specimens was low, while in patients with high L.I., postoperative recurrence and distant metastasis may occur more frequently, and postoperative supplementary therapies may be necessary, even when the tumor is completely resectable. In conclusion, Ki-67 staining is considered to be useful for evaluation of the malignant potential of HCC.</p></div>","PeriodicalId":13746,"journal":{"name":"International Hepatology Communications","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0928-4346(96)00345-3","citationCount":"6","resultStr":"{\"title\":\"Usefulness of monoclonal antibody Ki-67 as a prognostic factor of hepatocellular carcinoma\",\"authors\":\"Jiro Yoshimoto, Toyohito Iwata, Shigeru Takamori, Kuniaki Kojima, Shunji Futagawa\",\"doi\":\"10.1016/S0928-4346(96)00345-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We studied the proliferative activity of hepatocellular carcinoma (HCC) by immunohistochemical staining with Ki-67, a monoclonal antibody to nuclear protein observed in the proliferative period of the cell cycle, and evaluated the usefulness of Ki-67 as a prognostic factor. Of the patients who underwent hepatectomy for HCC at our department, 56 cases in which pathological studies for the tumor showed no degeneration or necrosis were selected. Immunohistochemical staining was performed according to the method of Shi et al., using MIB-1 monoclonal antibody (Immunotech, SA) as a primary antibody. Ki-67 L.I. was significantly higher in chronic hepatitis (CH) and liver cirrhosis (LC) than in normal liver, and the L.I. was also significantly higher in non-cancerous tissue of the patients with HCC than in tissues with other liver diseases. In patients with a history of portal hypertension, the L.I. in non-cancerous liver tissue was significantly lower at the previous operation for portal hypertension without HCC than that at the subsequent operation for HCC. The L.I. was significantly higher in patients who showed a high serum AFP level and in those who had intrahepatic metastasis. It also tended to be higher in patients with vessel invasion, infiltration to capsule, aneuploidy tumor cells, and poor differentiation. The cumulative survival rate was significantly lower in patients with the L.I. of 10% or higher than in those with the L.I. of less than 10% in cancerous region. Recurrence was observed earlier after hepatectomy in patients with higher L.I. and the L.I. was significantly higher in those who had recurrence within 12 months. In the patients who could be followed up, the L.I. was significantly higher in those who had multiple recurrence after hepatectomy than in those who had single-lesion recurrence. The incidence of HCC was higher in patients with CH or LC in which the proliferative activity was abnormally enhanced for a prolonged period, suggesting that hepatocyte hyperproliferation triggers hepatic carcinogenesis. In addition, long-term survival was expected even in patients with advanced HCC if the L.I. in preoperative biopsy specimens was low, while in patients with high L.I., postoperative recurrence and distant metastasis may occur more frequently, and postoperative supplementary therapies may be necessary, even when the tumor is completely resectable. In conclusion, Ki-67 staining is considered to be useful for evaluation of the malignant potential of HCC.</p></div>\",\"PeriodicalId\":13746,\"journal\":{\"name\":\"International Hepatology Communications\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0928-4346(96)00345-3\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Hepatology Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0928434696003453\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Hepatology Communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928434696003453","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Usefulness of monoclonal antibody Ki-67 as a prognostic factor of hepatocellular carcinoma
We studied the proliferative activity of hepatocellular carcinoma (HCC) by immunohistochemical staining with Ki-67, a monoclonal antibody to nuclear protein observed in the proliferative period of the cell cycle, and evaluated the usefulness of Ki-67 as a prognostic factor. Of the patients who underwent hepatectomy for HCC at our department, 56 cases in which pathological studies for the tumor showed no degeneration or necrosis were selected. Immunohistochemical staining was performed according to the method of Shi et al., using MIB-1 monoclonal antibody (Immunotech, SA) as a primary antibody. Ki-67 L.I. was significantly higher in chronic hepatitis (CH) and liver cirrhosis (LC) than in normal liver, and the L.I. was also significantly higher in non-cancerous tissue of the patients with HCC than in tissues with other liver diseases. In patients with a history of portal hypertension, the L.I. in non-cancerous liver tissue was significantly lower at the previous operation for portal hypertension without HCC than that at the subsequent operation for HCC. The L.I. was significantly higher in patients who showed a high serum AFP level and in those who had intrahepatic metastasis. It also tended to be higher in patients with vessel invasion, infiltration to capsule, aneuploidy tumor cells, and poor differentiation. The cumulative survival rate was significantly lower in patients with the L.I. of 10% or higher than in those with the L.I. of less than 10% in cancerous region. Recurrence was observed earlier after hepatectomy in patients with higher L.I. and the L.I. was significantly higher in those who had recurrence within 12 months. In the patients who could be followed up, the L.I. was significantly higher in those who had multiple recurrence after hepatectomy than in those who had single-lesion recurrence. The incidence of HCC was higher in patients with CH or LC in which the proliferative activity was abnormally enhanced for a prolonged period, suggesting that hepatocyte hyperproliferation triggers hepatic carcinogenesis. In addition, long-term survival was expected even in patients with advanced HCC if the L.I. in preoperative biopsy specimens was low, while in patients with high L.I., postoperative recurrence and distant metastasis may occur more frequently, and postoperative supplementary therapies may be necessary, even when the tumor is completely resectable. In conclusion, Ki-67 staining is considered to be useful for evaluation of the malignant potential of HCC.