Mallipatna Ashwin C, Dimaras Helen, Chan Helen S L, Héon Elise, Gallie Brenda L
Departments of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Ontario, Canada.
Arch Ophthalmol. 2011 Jun;129(6):738-45. doi: 10.1001/archophthalmol.2011.130.
To review the effectiveness and toxicity of periocular topotecan hydrochloride in fibrin sealant (Tisseel) for the control of intraocular retinoblastoma.
Retrospective medical record review of visually threatening or recurrent intraocular retinoblastoma treated with periocular topotecan.
Eight children (10 eyes) received 1 to 4 injections of periocular topotecan in fibrin sealant, without or with concomitant laser and/or single freeze-thaw prechemotherapy cryotherapy. Median dose was 0.18 mg/kg (3.72 mg/m(2)). The 6 children who responded to treatment had small discrete tumors (8 International Intraocular Retinoblastoma Classification group A or B eyes). Of these, prior primary treatment for 3 children (3 eyes) was laser; for 1 child (2 eyes), systemic chemotherapy with focal laser; and for 2 children (3 eyes), periocular topotecan. In 4 children (4 eyes), tumor regression was sufficient for effective focal therapy, but in 2 children (4 eyes), long-term control required systemic chemotherapy. The 2 children who did not respond each had an International Intraocular Retinoblastoma Classification group D eye treated primarily with systemic chemotherapy, focal laser, and cryotherapy and recurrent disease that was not controlled by periocular topotecan; both eyes were eventually enucleated. No ocular and minimal hematological toxic effects were observed. At 11 months' median follow-up after topotecan treatment (18 months since diagnosis), all 8 group A and B eyes were retained with ongoing focal therapy required in only 1 group B eye; the 2 group D eyes were enucleated.
Periocular topotecan in fibrin sealant can achieve volume reduction of small and recurrent retinoblastoma sufficient to allow successful focal therapy.
回顾眼周注射盐酸拓扑替康联合纤维蛋白封闭剂(Tisseel)治疗眼内视网膜母细胞瘤的有效性和毒性。
对接受眼周拓扑替康治疗的有视力威胁或复发性眼内视网膜母细胞瘤患者进行回顾性病历分析。
8名儿童(10只眼)接受了1至4次眼周注射盐酸拓扑替康联合纤维蛋白封闭剂治疗,同时或不同时进行激光治疗和/或单次冻融前化疗冷冻治疗。中位剂量为0.18mg/kg(3.72mg/m²)。6名治疗有效的儿童患有小的孤立性肿瘤(8只国际眼内视网膜母细胞瘤分类A或B组眼)。其中,3名儿童(3只眼)之前的主要治疗为激光治疗;1名儿童(2只眼)为全身化疗联合局部激光治疗;2名儿童(3只眼)为眼周拓扑替康治疗。4名儿童(4只眼)的肿瘤消退足以进行有效的局部治疗,但2名儿童(4只眼)的长期控制需要全身化疗。2名治疗无效的儿童各有1只国际眼内视网膜母细胞瘤分类D组眼,最初接受全身化疗、局部激光和冷冻治疗,复发性疾病未被眼周拓扑替康控制;最终两只眼均被摘除。未观察到眼部毒性和轻微血液学毒性。在拓扑替康治疗后的中位随访11个月(自诊断起18个月)时,所有8只A组和B组眼均得以保留,仅1只B组眼需要持续的局部治疗;2只D组眼被摘除。
眼周注射盐酸拓扑替康联合纤维蛋白封闭剂可使小的复发性视网膜母细胞瘤体积缩小,足以成功进行局部治疗。