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[使用包含丝裂霉素C的白蛋白微球进行肝动脉化疗栓塞治疗不可切除肝癌]

[Intra-arterial chemoembolization with albumin microspheres including mitomycin C in inoperable hepatic cancer].

作者信息

Endoh F

出版信息

Nihon Geka Gakkai Zasshi. 1987 May;88(5):584-93.

PMID:3037295
Abstract

Intra-arterial chemoembolization using mitomycin C microsphere (MMC MS) was carried out both for VX-2 tumor-bearing rabbits and for 19 patients with inoperable hepatic cancer. MMC MSs contain 5% MMC in albumin as a biodegradable drug carrier and an average diameter is 45 +/- 8 microns. VX-2 tumor, implanted into the hind legs of the rabbits, was treated intraarterially when it grew up to 2 cm in diameter. Tumor growth was compared with the other treated groups such as control, conventional MMC or blank microsphere; and MMC concentrations in the peripheral blood, femoral vein blood and muscles of the hind legs were measured after treatment. Tumor growth in the MMC MS group was remarkably retarded, but the other groups had no retardation. MMC concentrations of blood and muscle dropped below the assay limitation within 2 hours after conventional MMC injection, but in the animals treated with MMC MS, those showed the sustained drug release over for 6 hours. Fifteen patients with unresectable hepatic malignancies received intra-arterial hepatic infusion using conventional MMC, while 19 patients were treated by MMC MS infusion. Tumor regression in the 19 patients with MMC MS was seen in 42% (8/19), while that in the 15 with conventional infusion in 33% (5/15). Serum CEA levels in 12 patients with metastatic cancer decline from 57.7 +/- 72.2 ng/ml to 16.5 +/- 21.6 ng/ml 2 weeks after MMC MS treatment. However, those in 10 patients given conventional infusion dropped from 24.0 +/- 18.1 ng/ml to 17.4 +/- 18.0 ng/ml. The survival duration for patients given conventional infusion was 6.7 +/- 2.8 months, but that with MMC MS prolonged to 14.1 +/- 8.9 months. The MMC MS treatment for metastatic hepatic cancer had superiority to the conventional infusion treatment at p = 0.0040 in survival rate.

摘要

采用丝裂霉素C微球(MMC MS)对VX2荷瘤兔和19例无法手术切除的肝癌患者进行动脉内化疗栓塞。MMC MS在白蛋白中含有5%的MMC,作为可生物降解的药物载体,平均直径为45±8微米。将VX2肿瘤植入兔后腿,当其直径长到2厘米时进行动脉内治疗。将肿瘤生长情况与其他治疗组如对照组、传统MMC组或空白微球组进行比较;并在治疗后测量外周血、股静脉血和后腿肌肉中的MMC浓度。MMC MS组的肿瘤生长明显受到抑制,但其他组没有。传统MMC注射后2小时内,血液和肌肉中的MMC浓度降至检测限以下,但在接受MMC MS治疗的动物中,这些浓度显示持续释药超过6小时。15例不可切除的肝恶性肿瘤患者接受传统MMC动脉内肝灌注治疗,而19例患者接受MMC MS灌注治疗。19例接受MMC MS治疗的患者中,42%(8/19)出现肿瘤消退,而15例接受传统灌注治疗的患者中,33%(5/15)出现肿瘤消退。12例转移性癌症患者在MMC MS治疗2周后,血清癌胚抗原(CEA)水平从57.7±72.2 ng/ml降至16.5±21.6 ng/ml。然而,10例接受传统灌注治疗的患者血清CEA水平从24.0±18.1 ng/ml降至17.4±18.0 ng/ml。接受传统灌注治疗的患者生存时间为6.7±2.8个月,但接受MMC MS治疗的患者生存时间延长至14.1±8.9个月。MMC MS治疗转移性肝癌在生存率方面优于传统灌注治疗,p = 0.0040。

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