Harrington K J, Rowlinson-Busza G, Syrigos K N, Abra R M, Uster P S, Peters A M, Stewart J S
ICRF Oncology Unit, Imperial College of Science, Technology and Medicine, Hammersmith Hospital, 150 DuCane Road, London, W12 0HS, UK.
Br J Cancer. 2000 Sep;83(5):684-8. doi: 10.1054/bjoc.2000.1320.
The relationship between tumour size and uptake of(111)In-DTPA-labelled pegylated liposomes has been examined in a human head and neck cancer xenograft model in nude mice. The mean tumour uptake of(111)In-labelled pegylated liposomes at 24 hours was 7.2 +/- 6.6% ID/g. Liposome uptake for tumours < 0.1 g, 0.1-1.0 g and > 1.0 g was 15.1 +/- 10.8, 5.9 +/- 2.2 and 3.0 +/- 1.3% ID/g, respectively. An inverse correlation between tumour weight and liposome uptake was observed by both Spearman's rank correlation test (r(s)= - 0.573, P< 0.001) and Pearson's correlation coefficient (r(s)= - 0.555, P< 0.001). For 18 tumours with macroscopic central necrosis, the ratio of uptake in the tumour rim relative to the necrotic tumour core was 11.2 +/- 6.4. Measurement of tumour vascular volume for tumours of various sizes revealed an inverse correlation between tumour weight and tumour vascular volume (Spearman's rank correlation test, r(s)= - 0.598, P< 0.001), consistent with poor or heterogeneous vascularization of larger tumours. These data have important implications for the clinical application of pegylated liposome targeted strategies for solid cancers which are discussed in detail.
在裸鼠人头颈癌异种移植模型中,研究了肿瘤大小与¹¹¹In-DTPA标记的聚乙二醇化脂质体摄取之间的关系。24小时时¹¹¹In标记的聚乙二醇化脂质体的平均肿瘤摄取量为7.2±6.6% ID/g。肿瘤重量<0.1 g、0.1 - 1.0 g和>1.0 g时脂质体摄取量分别为15.1±10.8、5.9±2.2和3.0±1.3% ID/g。通过Spearman等级相关检验(r(s)= - 0.573,P<0.001)和Pearson相关系数(r(s)= - 0.555,P<0.001)均观察到肿瘤重量与脂质体摄取之间呈负相关。对于18个有肉眼可见中央坏死的肿瘤,肿瘤边缘与坏死肿瘤核心的摄取比为11.2±6.4。对各种大小肿瘤的肿瘤血管体积测量显示,肿瘤重量与肿瘤血管体积之间呈负相关(Spearman等级相关检验,r(s)= - 0.598,P<0.001),这与较大肿瘤血管生成不良或不均一相一致。这些数据对聚乙二醇化脂质体靶向策略在实体癌临床应用具有重要意义,将进行详细讨论。