Enhanced antitumor effects with intralymphatic delivery using bacillus Calmette-Guerin in animal models.

K A Jeglum, C Mangan, J E Wheeler
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引用次数: 6

Abstract

This study compares the effectiveness of various routes of administration of Bacillus Calmette-Guerin (BCG) utilizing the New Zealand white (NZW) rabbit V2 carcinoma model. The routes compared were intratumor, intravenous, scarification, subcutaneous, and intralymphatic. Primary tumor regression, disease-free interval, and survival were measured. The disease-free interval and survival for the intralymphatic group were significantly longer (p less than 0.05) than all groups except the scarification group. That group had a prolonged survival as compared with all groups except the intralymphatic group. The intralymphatic route of administration was the most effective method in causing local tumor regression and curtailing metastasis. This study clearly demonstrates that the intralymphatic route requires further mechanistic studies and clinical investigation as a means for delivering biological response modifiers.

卡介苗芽孢杆菌在动物模型中淋巴内给药增强抗肿瘤作用。
本研究采用新西兰白(NZW)兔V2癌模型,比较不同给药途径卡介苗(Bacillus Calmette-Guerin, BCG)的有效性。比较的途径是肿瘤内、静脉、切口、皮下和淋巴内。测量原发肿瘤消退、无病间期和生存率。除划伤组外,淋巴内组的无病间期和生存期均显著长于其他各组(p < 0.05)。与除淋巴内注射组外的其他各组相比,该组的存活时间更长。淋巴内给药是引起局部肿瘤消退和减少转移的最有效方法。这项研究清楚地表明,淋巴内途径需要进一步的机制研究和临床研究作为递送生物反应调节剂的手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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