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2.
Dig Endosc ; 36(4): 495, 2024 Apr.
Article in English | MEDLINE | ID: mdl-37986271
4.
BMC Surg ; 20(1): 201, 2020 Sep 14.
Article in English | MEDLINE | ID: mdl-32928172

ABSTRACT

BACKGROUND: We have previously shown the value of next-generation des-r-carboxy prothrombin (NX-DCP) for predicting vascular invasion in hepatocellular carcinoma (HCC). Since conventional DCP is inaccurate under some conditions, this study aimed to assess whether NX-DCP immunohistochemical staining was related to vascular invasion in HCC. METHODS: Fifty-six patients scheduled to undergo resection for single HCC were divided into two groups, with and without pathological portal vein invasion. Immunohistochemical features of HCC and sites of vascular invasion were assessed using alpha-fetoprotein (AFP), conventional DCP, and NX-DCP. RESULTS: Pathological portal vein invasion was absent in 43 patients and present in 13 patients. Patient characteristics, pathological background of the liver parenchyma, and tumor-related factors did not differ significantly between the groups. There was no significant difference in the serum AFP level between the groups, whereas levels of conventional DCP (p < 0.0001) and NX-DCP (p < 0.0001) were significantly higher in the vascular invasion group. Immunohistochemical staining showed no significant difference in the staining rate of tumor (67.9% vs. 80.7%, p = 0.08), but NX-DCP stained significantly more at the sites of vascular invasion (15.4% vs. 46.2%, p = 0.01) than conventional DCP. No vascular invasion was stained by AFP. CONCLUSIONS: NX-DCP offers better sensitivity for detecting sites of vascular invasion than AFP and conventional DCP.


Subject(s)
Carcinoma, Hepatocellular/diagnosis , Liver Neoplasms/diagnosis , Prothrombin , Biomarkers , Biomarkers, Tumor , Family Characteristics , Female , Humans , Male , Protein Precursors , alpha-Fetoproteins
5.
Biosci Trends ; 11(5): 581-587, 2017 Nov 20.
Article in English | MEDLINE | ID: mdl-29021421

ABSTRACT

Major portal vein invasion (MVI) by hepatocellular carcinoma (HCC) carries an extremely poor prognosis. Our aim was to clarify the indications of hepatic resection in the presence of MVI by HCC. Between 2001 and 2015, 1,306 patients undergoing primary treatment for HCC were analyzed (866 hepatic resections and 440 transarterial therapies). Significant prognostic factors were identified by retrospectively analyzing tumor status, liver function and treatment. Overall survival was compared in terms of the degree of vascular invasion and treatment. The 5-year survival rates according to the degree of vascular invasion (Vp) were Vp0: 51.9%, Vp1: 33.0%, Vp2: 16.7%, Vp3: 21.8%, and Vp4: 0%, respectively. Overall survival (OS) did not differ significantly between patients with Vp3 and Vp4 MVI (p = 0.153). Median survival following hepatic resection of Vp3 cases was significantly better than that for Vp4 cases (1,913 vs. 258 days, p = 0.014), while OS following transarterial therapy was not significantly different (164 vs. 254 days in Vp3 vs. Vp4, p = 0.137). Multivariate analysis revealed hepatic resection (Odds: 2.335 [95%CI: 1.236-4.718], p = 0.008) and multiple tumors (1.698 [1.029-2.826], p = 0.038) as independent predictors of survival. Hepatic resection in HCC patients with MVI should be indicate in patients with Vp3 invasion.


Subject(s)
Carcinoma, Hepatocellular/surgery , Hepatectomy/methods , Liver Neoplasms/surgery , Neovascularization, Pathologic/surgery , Portal Vein/surgery , Adult , Aged , Aged, 80 and over , Carcinoma, Hepatocellular/blood supply , Disease-Free Survival , Female , Hepatectomy/mortality , Humans , Liver Neoplasms/blood supply , Male , Middle Aged , Neoplasm Invasiveness , Neovascularization, Pathologic/pathology , Portal Vein/pathology , Prognosis , Retrospective Studies , Venous Thrombosis/pathology , Venous Thrombosis/surgery
6.
Br J Cancer ; 114(1): 53-8, 2016 Jan 12.
Article in English | MEDLINE | ID: mdl-26679378

ABSTRACT

BACKGROUND: In hepatocellular carcinoma (HCC), des-r-carboxy prothrombin (DCP) more accurately reflects the malignant potential than alpha-fetoprotein (AFP). Next-generation DCP (NX-DCP) was created to overcome some of the limitations of conventional DCP. This study assessed the predictive value of NX-DCP for vascular invasion in HCC. METHODS: We prospectively studied 82 consecutive patients who were scheduled to undergo resection for HCC. Patients were divided into two groups according to the presence or absence of pathological vascular invasion. The predictive powers of AFP, conventional DCP, and NX-DCP for vascular invasion were compared by receiver operating characteristic curve analysis, and correlations with tumour markers and the presence of vascular invasion were assessed. RESULTS: Vascular invasion was pathologically confirmed in 21 patients (positive group) and absent in 61 patients (negative group). The NX-DCP level was significantly higher in the positive group than in the negative group (510.0 mAU ml(-1) (10-98 450) vs 34.0 mAU ml(-1) (12-541), P<0.0001), while the AFP level did not differ significantly between the groups (9.7 ng ml(-1) (1.6-43 960.0) vs 11.0 ng ml(-1) (1.6-1650.0), P=0.49). The area under the curve (AUC) of NX-DCP (AUC=0.813, sensitivity=71.4%, 1-specificity=13.1%) had good sensitivity for the prediction of vascular invasion, while the AUC of AFP was 0.550 (sensitivity=28.6%, 1-specificity=1.60%). The suitable cutoff value for identifying pathological vascular invasion in HCC was 33 mm (AUC: 0.783, sensitivity=71.43%, 1-specificity=11.48%). CONCLUSIONS: The NX-DCP level can be used to predict the presence of vascular invasion in HCC.


Subject(s)
Biomarkers, Tumor/analysis , Biomarkers/analysis , Carcinoma, Hepatocellular/pathology , Liver Neoplasms/pathology , Protein Precursors/analysis , Prothrombin/analysis , Adult , Aged , Aged, 80 and over , Carcinoma, Hepatocellular/blood , Female , Humans , Liver Neoplasms/blood , Male , Middle Aged , Neoplasm Invasiveness , Prospective Studies , alpha-Fetoproteins/analysis
7.
Anticancer Res ; 31(11): 3991-3, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22110232

ABSTRACT

A 74-year-old female was found to have a 40-mm liver tumor (in segment VIII) by ultrasonography and was diagnosed with hepatocellular carcinoma (HCC). She underwent liver resection and was stably treated without recurrence for 19 months. A 45-mm extrahepatic tumor was then found during follow-up with enhanced computed tomography and was diagnosed as being a metachronous lymph node (LN) metastasis. Angiography revealed that the metastasis LN was fed by both the right and left gastric arteries. Transarterial chemotherapy with cisplatin was scheduled to control LN metastasis and to prevent intrahepatic metastasis, simultaneously. Blood alteration using coil embolization was performed to isolate the feeding arteries before transarterial chemotherapy with cisplatin powder. The patient was stably treated for 6 months (3 times) and no new intra- or extrahepatic metastatic lesions appeared during the chemotherapy. The patient subsequently underwent systematic LN dissection of the porta hepatis. She was successfully treated, and has remained recurrence-free for almost 5 years.


Subject(s)
Antineoplastic Agents/therapeutic use , Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/surgery , Cisplatin/therapeutic use , Liver Neoplasms/drug therapy , Liver Neoplasms/surgery , Aged , Carcinoma, Hepatocellular/secondary , Combined Modality Therapy , Female , Humans , Injections, Intra-Arterial , Liver Neoplasms/pathology , Lymphatic Metastasis , Tomography, X-Ray Computed , Treatment Outcome
8.
Gan To Kagaku Ryoho ; 37(12): 2699-701, 2010 Nov.
Article in Japanese | MEDLINE | ID: mdl-21224684

ABSTRACT

We performed transarterial chemoembolization (TACE) on the 67-year-old man who had hepatectomy for hepatocellular carcinoma with hepatitis C, recurrence in the liver and lymph nodes.The metastasis in lymph node did not show a clear increase until dying, and TACE showed the possibility of one treatment method to the metastasis in lymph node of the hepatocellular carcinoma.


Subject(s)
Carcinoma, Hepatocellular/pathology , Chemoembolization, Therapeutic , Liver Neoplasms/pathology , Lymphatic Metastasis , Aged , Humans , Male
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