PDT photo activation irradiance monitoring during a Phase I clinical study of TLD1433 in bladder cancer (Conference Presentation)

L. Lilge, Jenny Wu, A. Manalac, Jeffrey Cassidy, Wayne Embree, Roger White, A. Mandel, Vaughn Betz, M. Jewett, G. Kulkarni
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引用次数: 2

Abstract

While Photofrin mediated PDT for bladder cancer was the first approved indication for this technique, it failed to attract the confidence of urologists as a treatment option, primarily due to the high incidence of incontinence linked to PDT damage to the bladder muscle. To mitigate this hazard a phase I clinical trial using instillation of the Ru(II) coordination complex TLD1433 and 530 nm activation light was initiated. To achieve the intended drug doses of 0.35 and 0.7 mg/cm2 and a radiant exposure of 90 J/cm2 the concentration of the instillation was adjusted to each patients' bladder volume and the irradiance was measured at up to 12 positions in the bladder. Irradiance monitoring proved helpful in adjusting the irradiation time to the bladder wall albedo and also for increased light scattering and absorption due to turbidity built up in the bladder void. The initial multiplication factors of the bladders (n=6) ranged from 1.1 to 2.8. Monte Carlo simulations based on CT-scans from all 6 participants approximate the range of irradiances observed during these studies. Nevertheless, a fraction of the surface can see a multiple of the average irradiance whereas other regions (typically less than 5% of the surface area) see significantly less than the average irradiance. These variations are due to the actual bladder shape and are somewhat independent of the position of the spherical emitter. Fitting of the measured surface irradiance to the simulated dose surface histograms enables extraction of the bladder wall and bladder void’s optical properties.
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TLD1433治疗膀胱癌I期临床研究中的PDT光激活辐照度监测(会议报告)
虽然Photofrin介导的PDT治疗膀胱癌是该技术第一个被批准的适应症,但它未能吸引泌尿科医生作为一种治疗选择的信心,主要是因为PDT对膀胱肌肉的损伤导致尿失禁的高发生率。为了减轻这种危险,一项I期临床试验开始了,该试验使用Ru(II)配合物TLD1433和530 nm激活光进行滴注。为了达到0.35和0.7 mg/cm2的预期药物剂量和90 J/cm2的辐射照射,根据每位患者的膀胱体积调整了灌注浓度,并在膀胱中多达12个位置测量了辐照度。辐照度监测被证明有助于根据膀胱壁反照率调整照射时间,也有助于由于膀胱腔内浑浊而增加的光散射和吸收。膀胱的初始增殖因子(n=6)在1.1 ~ 2.8之间。基于所有6名参与者的ct扫描的蒙特卡罗模拟近似于这些研究中观察到的辐照度范围。然而,表面的一小部分可以看到平均辐照度的倍数,而其他区域(通常小于表面面积的5%)看到的辐照度明显低于平均辐照度。这些变化是由于实际的气囊形状,在某种程度上与球形发射器的位置无关。将测量的表面辐照度拟合到模拟的剂量表面直方图中,可以提取膀胱壁和膀胱空隙的光学特性。
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