ID | 83826 |
Title Transcription | ニクガンテキ モンミャク シンシュウ ヨウセイ カンガン セツジョゴ ノ Systemic IFN+Low dose FP ノ ユウヨウセイ : リロンテキ コンキョ ト リンショウテキ コウカ
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Title Alternative | Hepatic resection followed by systemic IFN plus low-dose FP for advanced HCC with macroscopic portal invasion : basic background and clinical outcome
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Author |
Imura, Satoru
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
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Hanaoka, Jun
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
Kanamoto, Mami
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
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Mori, Hiroki
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
Tokushima University Educator and Researcher Directory
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Ikemoto, Tetsuya
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
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Morine, Yuji
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
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Utsunomiya, Tohru
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
Shimada, Mitsuo
Department of Digestive Surgery and Transplantation, Tokushima University Hospital
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Keywords | hepatocellular carcinoma
portal vein tumor thrombus
interferon
chemotherapy
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Content Type |
Journal Article
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Description | Background and Aims : Despite a recent progress of treatment for hepatocellular carcinoma (HCC), the prognosis of advanced HCC with macroscopic vascular invasion remains unsatisfactory. We investigated anti-tumor effect of IFNα using experimental model and show the outcome of our systemic adjuvant therapy consisting of IFNα,5FU and cisplatin(IFP)after hepatectomy on advanced HCC with macroscopic portal invasion. Methods[: Basic study]Anti-tumor effects such as inhibition of invasion, proliferation of pegylated IFN α2b(PegIFNα)was evaluated using MH134mouse HCC cells, in vitro and vivo. [Clinical study]: Thirty patients who had HCC with Vp2or more of macroscopic portal invasion(Vp2; portal vein tumor thrombus in its2nd order branch)were included. Those patients were retrospectively divided into two groups : the systemic IFNα,5FU and cisplatin group (n=14, IFP group); and the no adjuvant therapy group(n=16, control). Clinicopathological variables were compared between the two groups, including patient survival and disease-free survival. Results[: Basic]In vitro, the proliferation was significantly suppressed by Peg-IFNα, and invasion potential was also inhibited. In vivo, tumor growth was significantly suppressed compared to control (0.5vs.5.0cm, p<0.05), and liver metastases was decreased(number :19vs.6, p<0.05). [Clinical]The overall and disease-free survival rate in IFP group was significantly higher than in control group(1y :100% vs38%,3y :65% vs25%, P<0.01,1y :36% vs25%,3y :36% vs19%, P<0.01). Regarding the recurrent patterns,5of9patients in IFP group had controllable tumors in the remnant liver, although12of13patients in control group had distant metastasis or multiple recurrences in the residual liver. Conclusion : Our new adjuvant regimen of systemic IFP may be a promising strategy after radical resection for HCC with macroscopic portal invasion.
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Journal Title |
四国医学雑誌
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ISSN | 00373699
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NCID | AN00102041
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Publisher | 徳島医学会
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Volume | 67
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Issue | 3-4
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Start Page | 147
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End Page | 154
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Sort Key | 147
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Published Date | 2011-08-25
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Remark | |
EDB ID | |
FullText File | |
language |
jpn
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TextVersion |
Publisher
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departments |
University Hospital
Medical Sciences
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