Hua Jiang, Gang Shen, Yizhou Jiang, Jing Zhang
Jinan University, Guangzhou, Guangdong, Department of Interventional Radiology and Vascular Anomalies Guangzhou Women and Children's Medical Center, Guangzhou, China.
Department of Interventional Radiology and Vascular Anomalies, Guangzhou Women and Children's Medical Center, Guangzhou, China.
J Cancer Res Ther. 2018 Jan;14(1):106-110. doi: 10.4103/jcrt.JCRT_722_17.
To evaluate the effectiveness and complications of intra-arterial chemotherapy (IAC) for treating advanced refractory retinoblastoma (RB) in a large single-center cohort.
Eighty-four eyes of 62 consecutive patients with advanced refractory RB who received IAC were included in the study during January 2013 and April 2015. These patients failed to respond adequately to a standard systemic chemotherapy (i.e., carboplatin, vincristine, and etoposide) with or without local therapy. Clinical outcomes and complications of these patients were reviewed.
All of these patients received IAC of melphalan combined with topotecan. The mean follow-up period was 14.2 months after final IAC (ranged from 3 to 28 months). The rate of eye preservation was 41.67% in Group D and 20.83% in Group E of this study. Short-term ocular adverse events included eyelid edema (n = 12, 14.29%), bulbar conjunctiva congestion (n = 25, 29.76%), and excessive tearing (n = 10, 11.90%). Long-term complications included vitreous hemorrhage (n = 7, 8%), subretinal hemorrhage (n = 9, 11%), retinal vasculopathy (n = 6, 7%), and ophthalmic artery spasm with reperfusion (n = 11, 13%). Fever was observed after IAC in 14 patients; transient vomiting was observed in 17 patients; there were 8 cases of transient myelosuppression.
IAC can be an optional treatment to save eyes of Group D RB that failed in systemic chemotherapy and were destined for enucleation. However, it should be cautioned for Group E. Both the ocular and systemic toxicities of IAC were within tolerance.
在一个大型单中心队列中评估动脉内化疗(IAC)治疗晚期难治性视网膜母细胞瘤(RB)的有效性和并发症。
2013年1月至2015年4月期间,纳入了62例接受IAC治疗的晚期难治性RB连续患者的84只眼。这些患者对含或不含局部治疗的标准全身化疗(即卡铂、长春新碱和依托泊苷)反应不佳。回顾了这些患者的临床结局和并发症。
所有这些患者均接受了美法仑联合拓扑替康的IAC治疗。末次IAC后平均随访期为14.2个月(范围3至28个月)。本研究中D组的眼球保留率为41.67%,E组为20.83%。短期眼部不良事件包括眼睑水肿(n = 12,14.29%)、球结膜充血(n = 25,29.76%)和流泪过多(n = 10,11.90%)。长期并发症包括玻璃体积血(n = 7,8%)、视网膜下出血(n = 9,11%)、视网膜血管病变(n = 6,7%)和眼动脉痉挛伴再灌注(n = 11,13%)。14例患者在IAC后出现发热;17例患者出现短暂呕吐;有8例短暂骨髓抑制。
IAC可作为挽救全身化疗失败且注定要摘除眼球的D组RB患者眼球的一种可选治疗方法。然而,对于E组患者应谨慎使用。IAC的眼部和全身毒性均在耐受范围内。