Sessler J L, Miller R A
Department of Chemistry & Biochemistry, University of Texas, Austin 78712, USA.
Biochem Pharmacol. 2000 Apr 1;59(7):733-9. doi: 10.1016/s0006-2952(99)00314-7.
The texaphyrins are quintessential metal-coordinating expanded porphyrins. They constitute a new series of synthetic porphyrin analogues that show promise as drugs for use in a range of medical therapies. Currently, two different water-solubilized lanthanide(III) texaphyrin complexes, namely the gadolinium(III) and lutetium(III) derivatives 1 and 2 (Gd-Tex and Lu-Tex, respectively), are being tested clinically. The first of these, XCYTRIN, is in a pivotal Phase III clinical trial as a potential enhancer of radiation therapy for patients with metastatic cancers to the brain receiving whole brain radiation therapy. The second, in various formulations, is being tested as a photosensitizer for use in: (i) the photodynamic treatment of recurrent breast cancer (LUTRIN; Phase II clinical trials complete), (ii) photoangioplastic reduction of atherosclerosis involving peripheral arteries (ANTRIN; now in Phase II testing), and (iii) light-based treatment of age-related macular degeneration (OPTRIN; currently in Phase I clinical trials), a vision-threatening disease of the retina. Taken in concert, these two metallotexaphyrins provide a powerful new class of experimental drugs whose diverse potential utility is abetted by a combination of well-optimized physical features, favorable tissue biolocalization characteristics, and novel mechanisms of action. Interestingly, these mechanisms may alter conventional wisdom regarding mechanisms of radiation therapy and the pathophysiology of atherosclerosis.
特沙卟啉是典型的金属配位扩展卟啉。它们构成了一系列新的合成卟啉类似物,有望作为多种医学疗法中的药物。目前,两种不同的水溶性镧系元素(III)特沙卟啉配合物,即钆(III)和镥(III)衍生物1和2(分别为Gd-Tex和Lu-Tex)正在进行临床试验。其中第一种,XCYTRIN,正在进行关键的III期临床试验,作为接受全脑放射治疗的脑转移癌患者放射治疗的潜在增强剂。第二种,有多种制剂,正在作为光敏剂进行测试,用于:(i)复发性乳腺癌的光动力治疗(LUTRIN;II期临床试验已完成),(ii)涉及外周动脉的动脉粥样硬化的光血管成形术减少(ANTRIN;现处于II期测试),以及(iii)年龄相关性黄斑变性的光基治疗(OPTRIN;目前处于I期临床试验),这是一种威胁视网膜视力的疾病。综合来看,这两种金属特沙卟啉提供了一类强大的新型实验药物,其多样的潜在用途得益于优化良好的物理特性、有利的组织生物定位特征和新颖的作用机制的组合。有趣的是,这些机制可能会改变关于放射治疗机制和动脉粥样硬化病理生理学的传统观念。