首页> 外文期刊>JAMA ophthalmology >Combined intravitreal melphalan and topotecan for refractory or recurrent vitreous seeding from retinoblastoma
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Combined intravitreal melphalan and topotecan for refractory or recurrent vitreous seeding from retinoblastoma

机译:玻璃体腔美法仑和托泊替康联合用于视网膜母细胞瘤难治性或复发性玻璃体播种

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IMPORTANCE Demonstrating the usefulness and complications of multiagent intravitreal chemotherapy is necessary for successful treatment in patients with recalcitrant vitreous seeding of retinoblastoma. OBJECTIVE To determine the efficacy and complications of combined intravitreal chemotherapy (melphalan hydrochloride and topotecan hydrochloride) for viable vitreous seeding from retinoblastoma. DESIGN, SETTING, AND PARTICIPANTS This retrospective studywas conducted in a hospital setting. Trans-pars plana intravitreal injection of melphalan hydrochloride (40 μg in 0.04mL of diluent) combined with topotecan hydrochloride (8-20 μg in 0.04mL of balanced salt solution) was performed in 9 eyes, followed by injection site cryotherapy. MAIN OUTCOMES AND MEASURES Complete regression of vitreous seeds of retinoblastoma. RESULTS Nine eyes, initially classified as Group D (n = 6) or E (n = 3) according to International Classification of Retinoblastoma categorization, received a standard 6 cycles of intravenous chemotherapy and/or intra-Arterial chemotherapy and subsequently developed recurrent viable vitreous seeds. Intravitreal administration of melphalan combined with topotecan produced complete control of vitreous seeds in all 9 eyes following a mean of 1.9 injections (median, 2; range, 1-3 injections). In 3 cases (33%), tumor control was achieved with a single injection, whereas in 6 (67%) cases, 2 or 3 injections were necessary. Three patients (33%) subsequently underwent enucleation because of recurrent tumor and persistent anterior chamber lesions. During a mean 15.2 months of follow-up (median, 16; range, 7-25 months), there was no recurrence of new tumor or vitreous seeds in the remaining 6 eyes. Complications included temporary hypotonia of 2 weeks or less (2 [22%]), temporary epithelial defect (1 [11%]), and vitreous hemorrhage (1 [11%]). There was no case of episcleral or orbital retinoblastoma extension or remote retinoblastoma metastasis. There was no change in the a and b waves of bright-flash electroretinograms. CONCLUSIONS AND RELEVANCE Administration of combined intravitreal melphalan and topotecan in eyes not subsequently enucleated appears to be safe and effective for resistant or recurrent vitreous seeds from retinoblastoma. In 3 of the cases (33%), tumor control was achieved with a single injection.
机译:重要说明要成功治疗视网膜母细胞瘤顽固性玻璃体植入的患者,必须进行多药玻璃体内化疗的有用性和并发症。目的探讨玻璃体内联合化疗(盐酸美法仑和盐酸拓扑替康)对成视网膜细胞瘤活体玻璃体植入的疗效和并发症。设计,场所和参与者这项回顾性研究是在医院进行的。在9只眼中经玻璃体玻璃体内注射盐酸美法仑(40μg在0.04mL稀释剂中)与盐酸托泊替康(8-20μg在0.04mL平衡盐溶液中)组合,然后进行冷冻部位注射。主要结果和措施视网膜母细胞瘤的玻璃体种子完全消退。结果根据国际视网膜母细胞瘤分类法,最初将9只眼睛分为D组(n = 6)或E(n = 3),接受了标准的6个周期的静脉内化疗和/或动脉内化疗,随后发展为复发性活玻璃体种子。玻璃体腔注射美法仑联合托泊替康可在平均1.9次注射(中位2次;范围1-3次注射)后完全控制所有9只眼的玻璃体种子。 3例(33%),单次注射即可达到肿瘤控制,而6例(67%),则需要2或3次注射。由于复发的肿瘤和持续的前房病变,三名患者(33%)随后接受了摘除术。在平均15.2个月的随访中(中位16个月;范围7到25个月),其余6眼没有新肿瘤或玻璃体种子复发。并发症包括2周或更短的暂时性肌张力降低(2 [22%]),暂时性上皮缺损(1 [11%])和玻璃体出血(1 [11%])。没有上皮或眼眶视网膜母细胞瘤扩展或远端视网膜母细胞瘤转移的病例。明亮的视网膜电图的a波和b波没有变化。结论和相关性玻璃体腔内美法仑和托泊替康联合给药后未摘除眼睛,对于成视网膜细胞瘤的抗药性或复发性玻璃体种子看来是安全有效的。在3例病例中(33%),单次注射即可实现肿瘤控制。

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