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多学科治疗对肝细胞癌的意义。

Significance of multidisciplinary therapy for hepatocellular carcinoma.

作者信息

Kawarada Y, Imai T, Iwata M, Yokoi H, Noguchi T, Mizumoto R

机构信息

First Department of Surgery, Mie University School of Medicine, Tsu, Japan.

出版信息

Cancer Chemother Pharmacol. 1992;31 Suppl:S13-9. doi: 10.1007/BF00687098.

DOI:10.1007/BF00687098
PMID:1333899
Abstract

The effect of multidisciplinary therapy for hepatocellular carcinoma (HCC) was evaluated in 121 resected cases. The 5-year survival was 100% for absolute curative resection (12 cases), 59.1% for relative curative resection (n = 37) and 10.9% for relative non-curative resection (n = 59). However, none of the patients survived for more than 3 years after absolute non-curative resection (n = 13). The non-recurrence in the preoperative TAE groups was different from that in non-TAE groups undergoing absolute and relative curative resection. The 1- and 3-year non-recurrence rates for relative non-curative resection were 92.3% and 53.8%, respectively, for the preoperative TAE group and 56.1% and 28.1%, respectively for the non-TAE group. These data show that preoperative TAE is effective in relative non-curative resection. Functional disturbances of the coagulation-fibrinolysis system in cirrhotic patients were improved after PSE. All patients undergoing hepatectomy after PSE had an uneventful postoperative course, including well-maintained function of the coagulation-fibrinolysis system and a decrease in splenic volume. At 1 year after hepatectomy, cirrhotic patients with critical liver function and poor coagulation-fibrinolysis showed appreciable hepatic regeneration. One patient died of hepatic failure 1 year after the operation. In recurrent HCC, the 1-, 2- and 3-year survival values after reresection were 100%, 75.0% and 25.0%, respectively. The respective values following TAE were 79.0%, 42.0% and 9.0%. Three cases of recurrent HCC were effectively treated, i.e., two patients achieved a partial response and one showed no change, by continuous intra-arterial infusion of 5-FU and lentinan with intermittent one-shot injections of epirubicin using a subcutaneous infusion pump. These three patients are alive at 1 year and 7 months, 1 year and 4 months and 6 months after the treatment, respectively.

摘要

对121例接受肝切除术的肝细胞癌(HCC)患者评估了多学科治疗的效果。绝对根治性切除术(12例)患者的5年生存率为100%,相对根治性切除术(n = 37)患者为59.1%,相对非根治性切除术(n = 59)患者为10.9%。然而,绝对非根治性切除术(n = 13)患者无一存活超过3年。术前经动脉栓塞化疗(TAE)组与接受绝对和相对根治性切除术的非TAE组的无复发生存情况不同。术前TAE组相对非根治性切除术的1年和3年无复发生存率分别为92.3%和53.8%,非TAE组分别为56.1%和28.1%。这些数据表明术前TAE在相对非根治性切除术中有效。经皮肝穿刺门静脉栓塞术(PSE)后,肝硬化患者凝血 - 纤溶系统的功能障碍得到改善。所有接受PSE后肝切除术的患者术后过程平稳,包括凝血 - 纤溶系统功能维持良好和脾体积减小。肝切除术后1年,肝功能临界且凝血 - 纤溶功能差的肝硬化患者显示出明显的肝再生。1例患者术后1年死于肝衰竭。在复发性HCC中,再次切除术后的1年、2年和3年生存率分别为100%、75.0%和25.0%。TAE后的相应生存率分别为79.0%、42.0%和9.0%。3例复发性HCC患者通过使用皮下输注泵持续动脉内输注5 - 氟尿嘧啶和香菇多糖并间歇性一次性注射表柔比星得到有效治疗,即2例患者部分缓解,1例病情无变化。这3例患者分别在治疗后1年7个月、1年4个月和6个月存活。

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Significance of multidisciplinary therapy for hepatocellular carcinoma.多学科治疗对肝细胞癌的意义。
Cancer Chemother Pharmacol. 1992;31 Suppl:S13-9. doi: 10.1007/BF00687098.
2
[Therapeutic value of hepatectomy and transcatheter arterial embolization (TAE) for hepatocellular carcinoma].[肝切除术及经导管动脉栓塞术(TAE)治疗肝细胞癌的疗效]
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[Evaluation of hepatectomy in small hepatocellular carcinoma--comparison with transcatheter arterial embolization therapy].小肝细胞癌肝切除术的评估——与经导管动脉栓塞治疗的比较
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Multi-disciplinary Concurrent Management of Recurrent Hepatocellular Therapy is Superior to Sequential Therapy.复发性肝细胞癌的多学科同步治疗优于序贯治疗。
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引用本文的文献

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Dendritic cells might be one of key factors for eliciting antitumor effect by chemoimmunotherapy in vivo.树突状细胞可能是体内化学免疫疗法引发抗肿瘤效应的关键因素之一。
Cancer Immunol Immunother. 2005 Feb;54(2):120-8. doi: 10.1007/s00262-004-0585-x. Epub 2004 Sep 22.
2
Changes in portal hemodynamics and hepatic function after partial splenic embolization (PSE) and percutaneous transhepatic obliteration (PTO).
Cancer Chemother Pharmacol. 1994;33 Suppl:S37-41. doi: 10.1007/BF00686666.
3
Prognosis after hepatic resection in patients with hepatocellular carcinoma, estimated on the basis of the morphometric indices.
Cancer Chemother Pharmacol. 1994;33 Suppl:S24-8. doi: 10.1007/BF00686663.

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