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肿瘤学中的肝脏栓塞术。综述。第二部分。动脉放射性栓塞术、门静脉栓塞术、实验性动脉栓塞程序。

Liver embolizations in oncology. A review. Part II. Arterial radioembolizations, portal venous embolizations, experimental arterial embolization procedures.

作者信息

Gunvén Peter

机构信息

Department of Oncology, Radiumhemmet, Karolinska University Hospital at Solna, Stockholm 171 76, Sweden.

出版信息

Med Oncol. 2007;24(3):287-96. doi: 10.1007/s12032-007-0040-x.

DOI:10.1007/s12032-007-0040-x
PMID:17873303
Abstract

Arterial embolization of the liver may temporarily retard the growth of its primary and secondary tumors which are both mainly nourished arterially. Addition of radioisotopes, mostly (131)I or (90)Y, results in radioembolizations which predominantly act by radiation and less by ischemia. They may therefore be utilized in the absence of portal venous flow when conventional embolization is hazardous. (131)I-oily radioembolization seems to prolong short-term survival in such patients with unresectable hepatocellular cancers, and to improve the prognosis after resection of hepatocellular cancer. The procedure does however not palliate better than "cold" chemoembolization in patients with preserved portal flow, except for having milder side effects. Embolization with (90)Y-coupled microspheres may shrink primary and secondary liver tumors but has so far unproven effects on survival. Embolization of portal venous branches gives compensatory hypertrophy of the non-embolized liver and can increase the volume of the future remnant liver before resection. This diminishes the risk for postoperative liver failure after extensive resection and/or in the presence of chronic liver disease, and permits wider surgical indications. Tumor growth may however be accelerated, and the hypertrophy is inhibited by severe liver parenchymal disease in which situation the method would be most needed. Experimental use of liver arterial embolizations includes combined arterial and portal embolizations, i.e. "chemical hepatectomy," arterial embolizations before external radiotherapy, administration of boron for neutron capture therapy, immunoembolizations, and future gene therapy.

摘要

肝脏动脉栓塞术可暂时延缓其原发性和继发性肿瘤的生长,这些肿瘤主要由动脉供血。添加放射性同位素,主要是(131)I或(90)Y,可导致放射性栓塞,其主要通过辐射起作用,缺血作用较小。因此,当传统栓塞术有风险时,在门静脉血流缺失的情况下可使用放射性栓塞术。(131)I油性放射性栓塞术似乎可延长此类无法切除的肝细胞癌患者的短期生存期,并改善肝细胞癌切除术后的预后。然而,在门静脉血流保留的患者中,该手术的缓解效果并不比“冷”化疗栓塞术更好,只是副作用较轻。用(90)Y偶联微球进行栓塞可使原发性和继发性肝肿瘤缩小,但迄今为止对生存期的影响尚未得到证实。门静脉分支栓塞可使未栓塞的肝脏发生代偿性肥大,并可在切除术前增加未来剩余肝脏的体积。这可降低广泛切除术后和/或存在慢性肝病时发生术后肝衰竭的风险,并允许更广泛的手术指征。然而,肿瘤生长可能会加速,而严重的肝实质疾病会抑制肥大,而在这种情况下该方法是最需要的。肝脏动脉栓塞术的实验应用包括动脉和门静脉联合栓塞,即“化学肝切除术”、外照射放疗前的动脉栓塞、用于中子俘获治疗的硼给药、免疫栓塞以及未来的基因治疗。

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本文引用的文献

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Radioembolization with yttrium-90 microspheres: a state-of-the-art brachytherapy treatment for primary and secondary liver malignancies: part 3: comprehensive literature review and future direction.钇-90微球放射性栓塞:原发性和继发性肝脏恶性肿瘤的先进近距离放射治疗:第3部分:综合文献综述与未来方向
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Radioembolization with 90yttrium microspheres: a state-of-the-art brachytherapy treatment for primary and secondary liver malignancies. Part 2: special topics.钇-90微球放射性栓塞:原发性和继发性肝脏恶性肿瘤的一种先进近距离放射治疗。第2部分:专题
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3
Radioembolization with 90Yttrium microspheres: a state-of-the-art brachytherapy treatment for primary and secondary liver malignancies. Part 1: Technical and methodologic considerations.
钇-90微球放射性栓塞:用于原发性和继发性肝脏恶性肿瘤的先进近距离放射治疗。第1部分:技术和方法学考量
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Radioembolization using 90Y-resin microspheres for patients with advanced hepatocellular carcinoma.使用90Y树脂微球对晚期肝细胞癌患者进行放射性栓塞治疗。
Int J Radiat Oncol Biol Phys. 2006 Nov 1;66(3):792-800. doi: 10.1016/j.ijrobp.2006.05.065. Epub 2006 Aug 14.
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Adenovirus vector-mediated gene transfer using degradable starch microspheres for hepatocellular carcinoma in rats.使用可降解淀粉微球介导腺病毒载体基因转移用于大鼠肝细胞癌治疗
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Portal vein embolisation prior to hepatic resection for colorectal liver metastases and the effects of periprocedure chemotherapy.结直肠癌肝转移灶肝切除术前的门静脉栓塞及围手术期化疗的效果
Br J Radiol. 2006 Jun;79(942):473-8. doi: 10.1259/bjr/29855825.
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Chemotherapy does not impair hypertrophy of the left liver after right portal vein obstruction.化疗不会损害右门静脉阻塞后左肝的肥大。
J Gastrointest Surg. 2006 Mar;10(3):365-70. doi: 10.1016/j.gassur.2005.09.001.
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Int J Radiat Oncol Biol Phys. 2006 Mar 1;64(3):745-50. doi: 10.1016/j.ijrobp.2005.09.007. Epub 2005 Nov 14.
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