Abd-El-Aal Hesham H
The Department of Oncology, Faculty of Medicine, Cairo University.
J Egypt Natl Canc Inst. 2006 Dec;18(4):357-62.
The present study evaluates the effect of pre-irradiation chemotherapy in pediatric patients with high risk medulloblastoma. Twenty-four (24) pediatric patients attended the pediatric unit of Kasr-El-Aini Center of Radiation Oncology and Nuclear Medicine (NEMROCK) from January 2000 to January 2003.
Our patients were 13 boys and 11 girls aged 3-12 years with a median of 6.5 years. According to Chang staging system 6 cases had T2, 14 cases had T3 A and 4 cases had T3 B, 20 cases were M0, 3 cases were M1 and 1 case was M2. All patients were treated by initial surgery, 2 cycles of pre-irradiation chemotherapy followed by craniospinal radiation then by 4 cycles of post-radiation chemotherapy.
Fifteen out of the 20 patients with M0 had objective response (10CR + 5PR) and no one had disease progression after pre-irradiation chemotherapy. Among 4 patients with M0 disease, 2 patients had PR and 2 had S.D. There was no disease progression among patients who received pre-irradiation chemotherapy. The 3-year overall survival and 3-year progression-free survival; (PFS) were 50% and 51%, respectively, Myelosuppression was the main toxic effect observed during pre-irradiation chemotherapy; however, there was no delay or interruption of craniospinal irradiation.
Pre-irradiation chemotherapy is effective in high risk medulloblastoma and is associated with acceptable side effects. The delay in craniospinal irradiation (CSI) for about 5 weeks to receive 2 courses of chemotherapy will not significantly increase disease progression. Multiple cycles of post-irradiation chemotherapy can be given safely after CSI. A larger number of patients and longer follow-up is needed to confirm the results.
本研究评估了放疗前化疗对高危型儿童髓母细胞瘤患者的疗效。2000年1月至2003年1月期间,24名儿童患者就诊于卡斯尔 - 艾尼放射肿瘤学与核医学中心(NEMROCK)的儿科病房。
我们的患者包括13名男孩和11名女孩,年龄在3至12岁之间,中位年龄为6.5岁。根据Chang分期系统,6例为T2期,14例为T3 A期,4例为T3 B期;20例为M0期,3例为M1期,1例为M2期。所有患者均接受了初始手术、2个周期的放疗前化疗,随后进行全脑全脊髓放疗,然后进行4个周期的放疗后化疗。
20例M0期患者中有15例出现客观缓解(10例完全缓解 + 5例部分缓解),且在放疗前化疗后无一人出现疾病进展。在4例M0期疾病患者中,2例部分缓解,2例病情稳定。接受放疗前化疗的患者中没有疾病进展情况。3年总生存率和3年无进展生存率(PFS)分别为50%和51%。骨髓抑制是放疗前化疗期间观察到的主要毒副作用;然而,全脑全脊髓放疗没有延迟或中断。
放疗前化疗对高危型髓母细胞瘤有效,且副作用可接受。延迟约5周进行全脑全脊髓放疗(CSI)以接受2个疗程的化疗不会显著增加疾病进展。在CSI后可以安全地给予多个周期的放疗后化疗。需要更多患者和更长时间的随访来证实结果。