Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.
J Neurosurg. 2011 Jun;114(6):1603-8. doi: 10.3171/2011.1.JNS10466. Epub 2011 Feb 4.
Retinoblastoma is the most common ocular neoplasm in children. Left untreated it spreads to the brain via the optic nerve. Traditional therapy is enucleation, and while this procedure is still the most common treatment worldwide, modern eye-preserving therapies can often spare the globe. However, patients with retinoblastoma often present in advanced stages of the disease when these globe-preserving strategies are often insufficient to prevent enucleation. In these challenging cases, direct infusion of chemotherapy into the ophthalmic artery has been attempted to achieve tumor control. The authors' aim in this study was to report on their initial experience with and clinical results for this approach.
The authors prospectively collected data on all cases of retinoblastoma treated with selective intraophthalmic melphalan at Bascom Palmer Eye Institute. All cases were classified as International Intraocular Retinoblastoma Classification (IIRC) Group D or Reese-Ellsworth Group Vb, had not responded to aggressive multimodal therapy consisting of chemotherapy and focal consolidating laser therapy, and were pending enucleation. Using digital subtraction angiography, a microcatheter was navigated under roadmap guidance into the ophthalmic artery, and melphalan was infused over 40 minutes. Early in the series, patients were treated with 3 or 5 mg of melphalan, but after low response rates occurred all eyes were treated with 7.5 mg of melphalan. All patients were examined with funduscopy while under anesthesia 3 weeks after treatment and every 3 months thereafter. Patients with persistent disease were retreated with repeat infusions of melphalan.
Twenty-six procedures were performed to treat 17 tumors in 15 patients. Successful cannulation of the ophthalmic artery was achieved in all cases. The follow-up ranged from 3 to 12 months, with a mean of 8.6 months. Overall, 76% of the tumors responded to therapy and these cases were spared enucleation. The average number of treatments was 1.5 per tumor. Of the responders, 54% responded to a single dose of melphalan. Treatment with the higher dose of 7.5 mg up front was associated with a lower enucleation rate (0% vs 36%) as compared with the lower starting dose. Delayed vitreous hemorrhage occurred after 4 (15%) of 26 treatments, and these cases were treated with enucleation.
In this challenging group of advanced retinoblastomas refractory to aggressive multimodal therapy, virtually 100% of eyes are generally enucleated. In contrast, the authors' protocol of infusing melphalan directly into the ophthalmic artery led to a dramatic decrease in the enucleation rate to 23.5%. While it is now the treatment of choice for refractory retinoblastoma at their center, its role in less advanced disease remains to be elucidated.
视网膜母细胞瘤是儿童中最常见的眼部肿瘤。如果不治疗,它会通过视神经扩散到大脑。传统的治疗方法是眼球摘除术,虽然这种手术仍然是全世界最常见的治疗方法,但现代的保眼治疗方法通常可以保留眼球。然而,患有视网膜母细胞瘤的患者通常在疾病的晚期出现,此时这些保眼策略往往不足以防止眼球摘除。在这些具有挑战性的病例中,已经尝试将化疗直接注入眼动脉以控制肿瘤。作者的目的是报告他们在使用这种方法方面的初步经验和临床结果。
作者前瞻性地收集了在巴斯科姆帕尔默眼科研究所接受选择性眼内美法仑治疗的所有视网膜母细胞瘤病例的数据。所有病例均被归类为国际眼内视网膜母细胞瘤分类(IIRC)组 D 或里斯-埃尔斯沃思组 Vb,对包括化疗和局部强化激光治疗在内的积极多模式治疗无反应,且需要眼球摘除。使用数字减影血管造影术,在 roadmap 引导下将微导管导航至眼动脉,并在 40 分钟内注入美法仑。在该系列的早期,患者接受 3 或 5mg 美法仑治疗,但在低反应率发生后,所有患者均接受 7.5mg 美法仑治疗。所有患者在治疗后 3 周麻醉下接受眼底镜检查,并在此后每 3 个月检查一次。对持续存在疾病的患者进行重复美法仑输注治疗。
26 例手术治疗了 15 例患者的 17 个肿瘤。所有病例均成功穿刺眼动脉。随访时间为 3 至 12 个月,平均为 8.6 个月。总的来说,76%的肿瘤对治疗有反应,这些肿瘤免于眼球摘除。肿瘤的平均治疗次数为 1.5 次。在有反应的患者中,54%的患者对单次美法仑剂量有反应。与较低的起始剂量相比,使用较高剂量的 7.5mg upfront 治疗与较低的眼球摘除率(0%比 36%)相关。26 次治疗中有 4 次(15%)发生延迟性玻璃体出血,这些病例接受了眼球摘除术。
在对积极多模式治疗无反应的晚期视网膜母细胞瘤这一具有挑战性的患者群体中,几乎 100%的患者通常需要眼球摘除。相比之下,作者直接将美法仑注入眼动脉的方案使眼球摘除率显著下降至 23.5%。虽然它现在是他们中心治疗难治性视网膜母细胞瘤的首选方法,但它在较不严重疾病中的作用仍有待阐明。