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72例标危型髓母细胞瘤放疗剂量对生存的影响
引用本文:甄子俊,路素英,夏云飞,吴少雄,王翦,朱佳,王娟,杨群英,孙晓非.72例标危型髓母细胞瘤放疗剂量对生存的影响[J].中华放射肿瘤学杂志,2015,24(5):540-543.
作者姓名:甄子俊  路素英  夏云飞  吴少雄  王翦  朱佳  王娟  杨群英  孙晓非
作者单位:510060 广州,华南肿瘤学国家重点实验室 中山大学肿瘤防治中心儿童肿瘤科(甄子俊、路素英、朱佳、王娟、孙晓非),放疗科(夏云飞、吴少雄),神经外科(王翦、杨群英)
摘    要:目的 回顾分析标危型髓母细胞瘤采用全脑全脊髓放疗剂量≤24 Gy和>24 Gy对预后的影响。方法 标危型髓母细胞瘤定义为年龄>3岁、未发生转移、肿瘤全切或近全切(残留≤1.5 cm3)。2003—2013年共入组72例初治儿童、青少年标危型髓母细胞瘤患者。患者术后接受全脑全脊髓+局部瘤床放疗和8个疗程辅助化疗,化疗方案为顺铂、司莫司汀或卡莫司汀联合长春新碱。按放疗剂量≤24 Gy和>24 Gy分为A、B组(20、52例),比较两组患者复发率和生存率。Kaplan-Meier法计算复发率和生存率并Logrank法检验组间差异。结果 A组接受全脑全脊髓放疗19.2~24.0 Gy,B组接受全脑全脊髓放疗24.1~30.6 Gy。放疗后66例(92%)患者完成全部辅助化疗。共11例患者复发。随访满3年患者48例,其中复发11例,死亡7例。全组3年EFS率为83%,3年OS率为86%。A组和B组患者3年EFS率分别为84%和83%(P=0.609), 3年OS率分别为85%和87%(P=0.963)。结论 标危型髓母细胞瘤经规范综合治疗效果较好,其中全脑全脊髓放疗剂量减少至19.2~24.0 Gy未影响疗效。

关 键 词:髓母细胞瘤  标危/放射疗法  髓母细胞瘤  标危/化学疗法  预后  

Impacts of radiation dose on survival in 72 patients with average-risk medulloblastoma
Zhen Zijun,Lu Suying,Xia Yunfei,Wu Shaoxiong,Wang Jian,Zhu Jia,Wang Juan,Yang Qunying,Sun Xiaofei.Impacts of radiation dose on survival in 72 patients with average-risk medulloblastoma[J].Chinese Journal of Radiation Oncology,2015,24(5):540-543.
Authors:Zhen Zijun  Lu Suying  Xia Yunfei  Wu Shaoxiong  Wang Jian  Zhu Jia  Wang Juan  Yang Qunying  Sun Xiaofei
Institution:Department of Pediatric Oncology,Sun Yet-sen University Cancer Center,State Key Laboratory of Oncology in South China,Guangzhou 510060, China
Abstract:Objective To retrospectively analyze the impacts of a craniospinal radiation dose ≤24 Gy or>24 Gy on the prognosis of patients with average-risk medulloblastoma. Methods Average-risk medulloblastoma was defined as non-metastatic cancer in children more than 3 years old with complete or near-complete (residual tumor ≤1.5 cm3) resection of tumor. A total of 72 children and adolescents with newly diagnosed average-risk medulloblastoma were enrolled as subjects from 2003 to 2013. After radical resection of the tumor, all patients received craniospinal plus local tumor bed radiotherapy and 8 cycles of adjuvant chemotherapy using cisplatin-, semustine-, or plus vincristine-based regimens. Patients exposed to a radiation dose ≤24 Gy were enrolled into Group A (n=20), while patients exposed to a radiation dose>24 Gy were enrolled into Group B (n=52). The recurrence rate and survival rate were compared between the two groups. The recurrence rate and survival rate were calculated using the Kaplan-Meier method and the differences between the two groups were analyzed using the log-rank test. ResultsPatients in Group A and Group B received craniospinal radiotherapy with a dose of 19.2-24.0 Gy and 24.1-30.6 Gy, respectively. After radiotherapy, 66 patients (92%) completed all adjuvant chemotherapy. A total of 11 patients were recurrence. In all patients, the 3-year sample size was 48;the 3-year event-free survival (EFS) and overall survival (OS) rates were 83% and 86%, respectively. There were no significant differences in the 3-year EFS and OS rates between Group A and Group B (84% vs. 83%, P=0.609;85% vs. 87%, P=0.963). Conclusions The standard comprehensive therapy achieves satisfactory treatment outcomes for average-risk medulloblastoma, in which a craniospinal radiation dose decreased to 19.2-24.0 Gy has no impacts on treatment outcomes.
Keywords:Medulloblastoma  average-risk/radiotherapy  Medulloblastoma  average-risk/chemotherapy  Prognosis  
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