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Ocular pharmacology of topotecan and its activity in retinoblastoma

机译:拓扑替康的眼药理作用及其在视网膜母细胞瘤中的活性

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PURPOSE:: To review the ocular pharmacology and antitumor activity of topotecan for the treatment of retinoblastoma by an evaluation of different routes of administration. METHODS:: Systematic review of studies available at PubMed using the keywords retinoblastoma, topotecan, and camptothecins, including preclinical data such as cell lines and animal models, as well as clinical studies in patients with retinoblastoma. RESULTS:: Forty-two available studies were reviewed. Evidence of antitumor activity against retinoblastoma as a single agent is based on data on cell lines and a limited number of affected patients with intraocular and extraocular disease when given in a protracted schedule. Evidence of additive or synergistic activity in combination with other agents such as carboplatin, melphalan, and vincristine was reported in preclinical and clinical models. In animal models, pharmacokinetic evaluation of topotecan administered by the periocular route shows that most of the drug reaches the vitreous through the systemic circulation. Topotecan administered by intravitreal injection shows high and sustained vitreal concentrations with limited systemic exposure and lack of retinal toxicity at a dose of up to 5 μg. Topotecan administered intraophthalmic artery shows higher passage to the vitreous compared with periocular administration in a swine model. CONCLUSION:: Topotecan alone or in combination is active against retinoblastoma. It shows a favorable passage to the vitreous when given intravenously and intraarterially, and ocular toxicity is minimal by all routes of administration. However, its clinical role, optimal dose, and route of administration for the treatment of retinoblastoma are to be determined.
机译:目的:通过评价不同的给药途径,综述托泊替康治疗视网膜母细胞瘤的眼药理学和抗肿瘤活性。方法:PubMed上使用关键词视网膜母细胞瘤,拓扑替康和喜树碱的研究的系统评价,包括临床前数据,例如细胞系和动物模型,以及视网膜母细胞瘤患者的临床研究。结果:审查了四十二项可用研究。单用抗视网膜母细胞瘤的抗肿瘤活性的证据是基于细胞系的数据,并且按时限给予有限数量的患眼内和眼外疾病的患者。在临床前和临床模型中报告了与其他药物(例如卡铂,美法仑和长春新碱)合用可产生累加或协同活性的证据。在动物模型中,通过眼周途径给药的拓扑替康的药代动力学评估表明,大多数药物通过全身循环到达玻璃体。通过玻璃体内注射给药的拓扑替康显示最高和持续的玻璃体浓度,全身暴露受限,并且在最高5μg的剂量下没有视网膜毒性。与猪模型中的眼周给药相比,托泊替康眼内动脉给药显示出更高的通过玻璃体的通道。结论:拓扑替康单独或联合使用对视网膜母细胞瘤具有活性。当静脉内和动脉内给药时,它显示出一条通往玻璃体的有利通道,并且所有给药途径对眼睛的毒性均最小。但是,要确定其临床作用,最佳剂量和治疗视网膜母细胞瘤的给药途径。

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