首页> 外文会议>5th International Photodynamic Association Biennial Meeting >Evaluation with mTHPC of early squamous cell carcinomas of the cheek pouch mucosa of Golden Syrian hamsters as a model for clinical PDT of early cancers in the u
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Evaluation with mTHPC of early squamous cell carcinomas of the cheek pouch mucosa of Golden Syrian hamsters as a model for clinical PDT of early cancers in the u

机译:用mTHPC评估金叙利亚仓鼠颊袋粘膜的早期鳞状细胞癌作为美国早期癌症临床PDT的模型

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Abstract: Golden Syrian hamsters are evaluated as an animal model for light induced fluorescence (LIF) photodetection and phototherapy of early squamous cell carcinomas of the upper aerodigestive tract, the esophagus, and the traecheo-bronchial tree. Carcinomas of this type are induced on the hamster cheek pouch mucosa by the application of the carcinogen 7,12-DMBA. For phototherapeutic experiments on the animals we utilized meso-(tetrahydoxyphenyl) chlorin (mTHPC). This drug is currently in phase I and II clinical trials for ENT patients presenting superficial `early' squamous cell carcinomas. By means of LIF we measured in vivo the kinetics of the uptake and removal of mTHPC in the normal and tumoral cheek mucosa and in the skin. The photodynamic therapy (PDT) reaction of the tissue after excitation of the photosensitizer with laser light at 652 nm was studied. Both pharmacokinetics and PDT efficacy are compared between animal model and clinical results with special emphasis on selectivity between normal and tumoral mucosa. These first experiments show that this tumor model in the hamster cheek pouch seems to be suitable for testing new photosensitizers preceding their clinical application as well as for optimization of the multiple parameters of clinical PDT. !5
机译:摘要:金叙利亚仓鼠被评估为光诱导荧光(LIF)光检测和光疗早期上消化道,鳞状细胞癌,食管和气管支气管树的动物模型。通过使用致癌物7,12-DMBA,可在仓鼠脸颊袋粘膜上诱发此类癌症。对于动物的光疗实验,我们使用了内消旋(四羟苯基)二氢卟酚(mTHPC)。该药物目前正在针对出现浅表“早期”鳞状上皮细胞癌的ENT患者进行I和II期临床试验。通过LIF,我们在体内测量了正常和肿瘤性颊粘膜和皮肤中mTHPC摄取和去除的动力学。研究了用652 nm激光激发光敏剂后组织的光动力疗法(PDT)反应。比较动物模型和临床结果之间的药代动力学和PDT功效,并特别强调正常和肿瘤黏膜之间的选择性。这些最初的实验表明,仓鼠脸颊袋中的这种肿瘤模型似乎适合于在临床应用之前测试新的光敏剂,以及优化临床PDT的多个参数。 !5

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