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Development of a new multi-modality therapy for far advanced hepatocellular carcinoma : a combined therapy of a new percutaneous local tumor ablation and a chemotherapy using subcutaneously embedded port for arterial infusion or gene therapy

Research Project

Project/Area Number 10670454
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Gastroenterology
Research InstitutionUniversity of Tokyo

Principal Investigator

SHIINA Shuichiro  University of Tokyo Hospital, Instructor, 医学部・付属病院, 助手 (70251238)

Co-Investigator(Kenkyū-buntansha) OMATA Masao  University of Tokyo Hospital, Chairman, 医学部・付属病院, 教授 (90125914)
MATSUMURA Masayuki  Institute of Adult Disease, Asahi Life Foundation, Director, 消化器科, 医長
KATO Naoya  University of Tokyo Hospital, Instructor, 医学部・付属病院, 助手 (90313220)
金井 文彦  東京大学, 医学部・附属病院, 医員
Project Period (FY) 1998 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2000: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥1,300,000 (Direct Cost: ¥1,300,000)
KeywordsFar advanced hepatocellular carcinoma / Multi-modality therapy / Percutaneous tumor ablation / Subcutaneously embedded port for arterial infusion / Chemotherapy / Gene therapy / Radio-frequency ablation / 肝細胞癌 / 皮下埋込式動注ポート / radiofrequency ablation / low dose FP療法 / 集学的治療
Research Abstract

The aim of this study was to develop a new multi-modality therapy for far advanced hepatocellular carcinoma, which had been treated non-curatively only by transcatheter arterial embolization or supportive therapy because of wide spread of the cancer. We wanted to develop a combined therapy of a new percutaneous local tumor ablation and a chemotherapy using subcutaneously embedded port for arterial infusion or gene therapy.
With regard to development of a new percutaneous tumor ablation, we have performed radio-frequency ablation(RFA)on a total of 400 cases since we introduced it in February 1999. In RFA, we can surely obtain a necrotic area of 3 cm in diameter by a 12-minute ablation. In most cases, one or two treatment sessions are enough to achieve a complete necrosis of the lesion with a safety margin, which results in a shorter hospitalization. We think more than 95% of cases treated by percutaneous tumor ablation will be treated by RFA in the near future. Thus we would like to gain more know-how to perform RFA.
With regard to optimization of chemotherapy, we performed "low dose FP" chemotherapy using subcutaneously embedded port for arterial infusion and have been analyzing data to evaluate factors which contributed the chemotherapeutic efficacy. The final goal is to predict therapeutic efficacy before the treatment. To do this, we would use DNA tips in the future. We have also used a new chemotherapeutic regimen of 5-FU and interferon. We will use the regimen on more cases and evaluate its efficacy.
We have used nude mice to examine usefulness and safety of a gene therapy in order to introduce it to a clinical trial. However, we have not achieved satisfactory results yet.

Report

(4 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • 1998 Annual Research Report
  • Research Products

    (28 results)

All Other

All Publications (28 results)

  • [Publications] Shiina S, et al.: "Non-Surgical Treatment of Hepatocellular Carcinoma : from Percutaneous Ethanol lnjection Therapy (PEIT). Percutaneous Microwave Coagulation Therapy (PMCT) to Radio-Frequency Ablation (RFA)"Oncology. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shiina S, et al.: "Percutaneous ethanol injection therapy (PEIT) for liver tumors"Eur J Ultrasound. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Koike Y, Shiina S, et al.: "Risk factors for recurring hepatocellular carcinoma differ according to infected hepatitis virus-An analysis of 236 consecutive patients with a single lesion."Hepatology.. 32. 1216-1223 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yamagata M, Shiina S, et al.: "Serum endostatin levels in patients with hepatocellular carcinoma."Ann Oncol.. 11. 761-762 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yoshida H, Shiina S, et al.: "Poor association of TT virus viremia with hepatocellular carcinoma."Liver. 20. 247-252 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hamamura K, Shiina S, et al.: "Unique clinical characteristics of patients with hepatocellular carcinoma who pressnt with high plasma des-gamma-carboxy prothrombin and low serum alpha-fetoprotein."Cancer.. 88. 1557-1564 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Obi S, Shiina S, et al: "Early detection of haemobilia associated with percutaneous ethanal injection for hepatocellular carcinoma."Eur J Gastroenterol Hepatol. 12. 285-290 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shiina S, et al.: "Non-Surgical Treatment of Hepatocellular Carcinoma : from Percutaneous Ethanol Injection Therapy(PEIT), Percutaneous Microwave Coagulation Therapy(PMCT)to Radio-Frequency Ablation(RFA)"Oncology. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shiina S, et al.: "Percutaneous ethanol injection therapy(PEIT)for liver tumors."Eur J Ultrasound. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Koike Y, Shiina S, et al.: "Risk factors for recurring hepatocellular carcinoma differ according to infected hepatitis virus-An analysis of 236 consecutive patients with a single lesion."Hepatology.. 32. 1216-23 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yamagata M, Shiina S, et al.: "Serum endostatin levels in patients with hepatocellular carcinoma."Ann Oncol.. 11. 761-2 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yoshida H, Shiina S, et al.: "Poor association of TT virus viremia with hepatocellular carcinoma."Liver. 20. 247-52 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Obi S, Shiina S, et al.: "Early detection of haemobilia associated with percutaneous ethanol injection for hepatocellular carcinoma."Eur J Gastroenterol Hepatol.. 12. 285-90 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hamamura K, Shiina S, et al.: "Unique clinical characteristics of patients with hepatocellular carcinoma who present with high plasma des-gamma-carboxy prothrombin and low serum alpha-fetoprotein."Cancer.. 88. 1557-64 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Shiina S, et al.: "Non-Surgical Treatment of Hepatocellular Carcinoma : from Percutaneous Ethanol Injection Therapy (PEIT), Percutaneous Microwave Coagulation Therapy (PMCT) to Radio-Frequency Ablation (RFA)"Oncology. (in press).

    • Related Report
      2000 Annual Research Report
  • [Publications] Shiina S, et al.: "Percutaneous ethanol injection therapy (PEIT) for liver tumors"Eur J Ultrasound. (in press).

    • Related Report
      2000 Annual Research Report
  • [Publications] Koike Y,Shiina S, et al.: "Risk factors for recurring hepatocellular carcinoma differ according to infected hepatitis virus-An analysis 236 consecutive patients with a single lesion."Hepatology.. 32. 1216-1223 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yamagata M,Shiina S, et al.: "Serum endostatin levels in patients with hepatocellular carcinoma."Ann Oncol.. 11. 761-762 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yoshida H,Shiina S, et al.: "Poor association of TT virus viremia with hepatocellular carcinoma."Liver. 20. 247-252 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Hamamura K,Shiina S, et al.: "Unique clinical characteristics of patients with hepatocellular carcinoma who present with high plasma des-gamma-carboxy prothrombin and low serum alpha-fetoprotein."Cancer.. 88. 1557-1564 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 椎名秀一朗、他: "Cod tip型電極を用いた経皮的ラジオ波焼灼療法による肝細胞癌の治療"肝臓. 41. 24-30 (2000)

    • Related Report
      1999 Annual Research Report
  • [Publications] 椎名秀一朗、他: "大型肝細胞癌に対する経皮的エタノール注入療法(PEIT)"臨床消化器内科. 14. 178-181 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] 椎名秀一朗、他: "肝細胞癌に対する経皮的エタノール注入療法(PEIT)"総合臨床. 48. 290-295 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Imamura M,Shiina S,et al.: "Percutaneous hepatic infarction therapy for hepatocellular caricnoma." AJR. 171. 1031-1035 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Imamura M,Shiina S,et al.: "Power Doppler sonongraphy for hepatocellular carcinoma:factors affecting the power Doppler singals of the tumors" Liver. 18. 427-433 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 椎名秀一朗、今村雅俊、他: "大腸癌肝転移に対する経皮的局所療法" 肝胆膵. 37. 649-653 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 椎名秀一朗、寺谷卓馬: "肝癌の治療---経皮的局所療法" 臨床成人病. 28. 1518-1520 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 椎名秀一朗、今村雅俊、他: "肝癌の経皮的エタノール注入療法(PEIT)・経皮的マイクロ波凝固療法(PMCT)……一般施設と専門施設での選択はどうあるべきか" Medical Practice. 15. 1223-1228 (1998)

    • Related Report
      1998 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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