Division of Hematology-Oncology, Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Pediatr Blood Cancer. 2024 Jan;71(1):e30718. doi: 10.1002/pbc.30718. Epub 2023 Oct 10.
Intra-arterial chemotherapy (IA) as a treatment to salvage the eye with advanced retinoblastoma is increasingly utilized based on successes reported by institutions around the world mainly through retrospective studies.
To study the feasibility of delivering melphalan directly into the ophthalmic artery in a multi-institutional prospective study in children with newly diagnosed unilateral group D retinoblastoma.
The Children's Oncology Group (COG) initiated study ARET12P1 in 2014 and was open to nine institutions. Eligible patients older than six months of age were enrolled. The feasibility of delivering three injections of melphalan into the ophthalmic artery every 28 days was assessed.
Nine institutions participated in this trial. Fourteen patients were enrolled, two of whom were unevaluable for feasibility. Four patients experienced a feasibility failure. In two patients, the ophthalmic artery could not be accessed for the second IA injection, in one the artery could not be accessed for the first injection, and one patient experienced grade 4 hypotension during the procedure.
Delivery of prescribed therapy within the context of this study did not meet the feasibility goals of the study with only a 67% feasibility success rate. These results should caution centers that plan to initiate this treatment and suggest investment in training to achieve technical expertise or referral to centers with expertise.
基于世界各地医疗机构的成功经验,国际上越来越多地采用经动脉化疗(IA)来挽救晚期视网膜母细胞瘤患者的眼睛,这些成功经验主要来自回顾性研究。
在一项多机构、前瞻性研究中,评估向新诊断的单侧 D 组视网膜母细胞瘤患儿的眼动脉直接给予氨甲蝶呤的可行性。
儿童肿瘤协作组(COG)于 2014 年启动了 ARET12P1 研究,共 9 家机构参与。纳入年龄大于 6 个月的合格患者。评估每 28 天经动脉给予 3 次氨甲蝶呤的可行性。
9 家机构参与了这项试验。共纳入 14 名患者,其中 2 名因可行性问题无法评估。4 名患者出现可行性失败。在 2 名患者中,第二次 IA 注射无法进入眼动脉,1 名患者第一次注射无法进入动脉,1 名患者在手术过程中出现 4 级低血压。
在这项研究中,按规定给予治疗的情况下,可行性仅达到 67%,未达到研究目标。这些结果应提醒计划开展这种治疗的中心,建议投资于培训以获得技术专长,或转介至具有专业知识的中心。