Zelter M, Damel A, Gonzalez G, Schwartz L
Ophthalmology Unit, Hospital de Niños de Buenos Aires, Argentina.
Cancer. 1991 Oct 15;68(8):1685-90. doi: 10.1002/1097-0142(19911015)68:8<1685::aid-cncr2820680804>3.0.co;2-o.
Seventy-two patients with retinoblastoma (RTB) (unilateral [47 patients] and bilateral [25 patients]) were studied for a period of 6 years. Treatment consisted of enucleation of those eyes that had severe involvement and was followed by radiation therapy and/or chemotherapy (systemic or intrathecal) according to clinical pathologic staging. All patients who underwent nonsurgical treatment received systemic chemotherapy. Intrathecal chemotherapy was administered when there was involvement of the central nervous system. Nonsurgical treatment consisted of radiation therapy and/or light coagulation, followed by enucleation if there was no response. The overall survival rates were 79% for unilateral disease (median follow-up time, 63 months) and 72% for bilateral disease (median follow-up time, 81 months). Vision was regained in 14 of 21 conserved eyes.
对72例视网膜母细胞瘤(RTB)患者(单侧47例,双侧25例)进行了为期6年的研究。治疗方法包括对严重受累的眼睛进行眼球摘除术,然后根据临床病理分期进行放射治疗和/或化疗(全身或鞘内化疗)。所有接受非手术治疗的患者均接受全身化疗。当中枢神经系统受累时给予鞘内化疗。非手术治疗包括放射治疗和/或光凝治疗,如无反应则随后进行眼球摘除术。单侧疾病的总生存率为79%(中位随访时间63个月),双侧疾病的总生存率为72%(中位随访时间81个月)。21只保留的眼睛中有14只恢复了视力。