Xiao Zhengwen, Dickey Dwayne, Owen Richard J, Tulip John, Moore Ronald
Department of Oncology, University of Alberta, Edmonton, Alberta, Canada.
J Urol. 2007 Jul;178(1):308-13. doi: 10.1016/j.juro.2007.03.008. Epub 2007 May 17.
We determined the feasibility of complete treatment of the canine prostate and long-term effectiveness of interstitial photodynamic therapy using the intra-arterial photosensitizer QLT0074 (benzoporphyrin derivative 1,3-diene C,D-diethylene glycol ester A ring) (QLT, Vancouver, British Columbia, Canada) administration and pulsed light delivery.
The prostate gland of 11 dogs were infused with QLT0074 via the prostatovesical arteries (2 mg drug per artery bilaterally) under fluoroscopic guidance. Immediately following infusion the prostate was surgically exposed and 7 optical fibers with 1.5 cm cylindrical diffusers in after loading sheaths were inserted into the prostate through a template. Light was delivered sequentially to the optic fibers via a computer driven switch system. One dog was sacrificed 6 days after photodynamic therapy to assess acute tissue effects. The other 10 dogs were monitored for clinical tolerance and urinary function, and sacrificed at between 3 and 11 months. Prostate specimens were examined microscopically to evaluate long-term tissue reactions.
Comprehensive destruction of the prostate was noted in the acute dog. Except for urinary retention and mild hematuria no other perioperative complications were observed in the chronic dogs. Urodynamic examination did not reveal deleterious bladder and urethral function. Average prostate volume decreased 71% at 3 months and 56% after 6 months (p=0.007 and 0.014, respectively). Microscopic evaluation revealed prostate glandular epithelial atrophy, stromal fibrosis and mononuclear cell infiltration.
Interstitial photodynamic therapy using intra-arterial QLT0074 and pulsed light delivery is safe and feasible for comprehensive destruction of the canine prostate. Clinical trials are required to confirm it for managing prostate diseases.
我们确定了使用动脉内注射光敏剂QLT0074(苯并卟啉衍生物1,3 - 二烯C,D - 二甘醇酯A环)(QLT,加拿大不列颠哥伦比亚省温哥华)给药及脉冲光照射来完全治疗犬前列腺的可行性以及间质光动力疗法的长期有效性。
在荧光镜引导下,通过前列腺膀胱动脉向11只犬的前列腺注入QLT0074(每侧动脉注入2mg药物)。注入后立即通过手术暴露前列腺,并通过模板将7根带有1.5cm圆柱形扩散器的光纤经后装鞘插入前列腺。通过计算机驱动的开关系统依次向光纤输送光。1只犬在光动力治疗后6天处死以评估急性组织效应。另外10只犬监测临床耐受性和排尿功能,并在3至11个月时处死。对前列腺标本进行显微镜检查以评估长期组织反应。
在急性实验犬中观察到前列腺的全面破坏。除慢性实验犬出现尿潴留和轻度血尿外,未观察到其他围手术期并发症。尿动力学检查未发现膀胱和尿道功能有害变化。3个月时前列腺平均体积减少71%,6个月后减少56%(分别为p = 0.007和0.014)。显微镜评估显示前列腺腺上皮萎缩、间质纤维化和单核细胞浸润。
使用动脉内注射QLT0074及脉冲光照射的间质光动力疗法对犬前列腺进行全面破坏是安全可行的。需要进行临床试验以证实其对前列腺疾病的治疗作用。