Very long-term of survival, 5 years and more in diffuse intrinsic pontine brainstem gliomas in children and adolescents treated with Radiotherapy and Nimotuzumab

Alert J, C. I, Valdes J, Ropero R, Perez M, Garcia D D, Forteza M, Avila J
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Abstract

Diffuse intrinsic brainstem gliomas have a bad prognosis, and short-term survival time. Radiotherapy has been the principal treatment, and chemotherapy has not improved outcome. The anti –EGFR monoclonal antibody Nimotuzumab combined with Radiotherapy was tested in a series of 41 children and adolescents with diffuse intrinsic pontine gliomas (DIPG) included between January 2008 and December 2015 and a follow-up till January 2021.They were irradiated in the Instituto Nacional de Oncologia y Radiobiologia, Havana, Cuba with a median dose of 54 Gy. Nimotuzumab was applied at a dose of 150 mg/m2, weekly during the period of irradiation, then every 2 weeks by 8 doses, and them monthly for 1,2 or more years. A response was observed in 87.8% of patients. Prolonged use of Nimotuzumab was feasible and well tolerated. Median age at diagnosis was 7 years old, median survival was 18.8 months. There were minor toxicities, only Grade I or II. Survival rate at 5 years was 34.1%, stablished till years or more. Two relapsing patients were re-irradiated. The combination of irradiation and Nimotuzumab is an option to increase survival in DIPG.
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放疗和尼莫单抗治疗的儿童和青少年弥漫性脑桥脑干胶质瘤的长期生存期为5年以上
弥漫性脑干胶质瘤预后差,生存时间短。放疗是主要的治疗方法,化疗并没有改善预后。抗egfr单克隆抗体Nimotuzumab联合放疗在41例弥漫性内禀脑桥胶质瘤(DIPG)儿童和青少年中进行了测试,时间为2008年1月至2015年12月,随访至2021年1月。他们在古巴哈瓦那的国家肿瘤放射生物学研究所接受了中位剂量54戈瑞的放射治疗。尼莫妥珠单抗的剂量为150mg /m2,在辐照期间每周使用,然后每2周使用8次,每月使用一次,持续1、2年或更长时间。87.8%的患者有应答。长期使用尼莫妥珠单抗是可行的,并且耐受性良好。诊断时中位年龄为7岁,中位生存期为18.8个月。有轻微的毒性,只有一级或二级。5年生存率为34.1%,≥5年。2例复发患者再次接受放射治疗。放疗联合尼妥珠单抗是提高DIPG患者生存率的一种选择。
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