Verschuur A C, Grill J, Lelouch-Tubiana A, Couanet D, Kalifa C, Vassal G
Department of Paediatric Oncology, Institut Gustave Roussy, 39 rue Camille Desmoulins, 94805 Villejuif, France.
Br J Cancer. 2004 Aug 2;91(3):425-9. doi: 10.1038/sj.bjc.6601997.
This report describes a single-centre study with temozolomide (TMZ) (200 mg m(-2) day(-1) x 5 per cycle of 28 days) in children with (recurrent) high-grade glioma. Magnetic resonance imaging was performed every two cycles. In all, 20 patients were treated between 1998 and 2001 after the UKCCSG/SFOP TMZ phase II trial. All patients had measurable disease. Totally, 15 patients had a relapse after surgery+/-radiotherapy+/-chemotherapy. Overall, five patients received TMZ after surgery or biopsy, awaiting radiotherapy. There were one clinically malignant grade II glioma, 11 grade III and eight grade IV gliomas. Seven tumours had oligodendroglial features. Mean age at start of TMZ was 12.0 years (range 3-20.5 years). In total, eight patients had >8 cycles (range 3-30). One VGPR (currently in CR after surgery), three PRs (with a PFS of 4, 4 and 11 months, respectively) and one MR (PFS 14 months) were observed. Three out of five responses occurred after >4 courses. The overall response rate was 20%. Median progression-free survival (PFS) was 2.0 months (range 3 weeks-34+ months). PFS rate was 20% after 6 months. Median overall survival (OS) was 10 months. Nine patients showed a clinical improvement. Three patients vomitted shortly after TMZ administration, eight patients (13 cycles) experienced grade III/IV thrombocytopenia, occurring predominantly during the fourth week of the first two cycles. Five patients experienced neutropenia, and three patients febrile neutropenia. TMZ is a well-tolerated ambulatory treatment for children with malignant glial tumours. This drug warrants further study in these highly chemoresistant tumours and should be studied either as upfront therapy or in combination therapy.
本报告描述了一项针对(复发性)高级别胶质瘤儿童患者使用替莫唑胺(TMZ)(200 mg m(-2) 每日1次,每28天为1个周期,共5天)的单中心研究。每两个周期进行一次磁共振成像检查。1998年至2001年期间,在英国儿童癌症协作组/法国儿科肿瘤学会TMZ II期试验后,共有20例患者接受了治疗。所有患者均有可测量的病灶。总共有15例患者在手术±放疗±化疗后复发。总体而言,5例患者在手术或活检后接受TMZ治疗,等待放疗。其中有1例临床诊断为恶性II级胶质瘤,11例III级和8例IV级胶质瘤。7个肿瘤具有少突胶质细胞特征。开始使用TMZ时的平均年龄为12.0岁(范围3 - 20.5岁)。总共有8例患者接受了超过8个周期的治疗(范围3 - 30个周期)。观察到1例非常好的部分缓解(VGPR,目前术后处于完全缓解[CR]状态)、3例部分缓解(PR,无进展生存期[PFS]分别为4、4和11个月)和1例疾病稳定(MR,PFS为14个月)。5例缓解中有3例在超过4个疗程后出现。总体缓解率为20%。中位无进展生存期(PFS)为2.0个月(范围3周 - 34 +个月)。6个月时的PFS率为20%。中位总生存期(OS)为10个月。9例患者临床症状改善。3例患者在服用TMZ后不久出现呕吐,8例患者(13个周期)出现III/IV级血小板减少,主要发生在前两个周期的第四周。5例患者出现中性粒细胞减少,3例患者出现发热性中性粒细胞减少。对于患有恶性胶质细胞瘤的儿童,TMZ是一种耐受性良好的门诊治疗药物。该药物在这些高度耐药的肿瘤中值得进一步研究,应作为一线治疗或联合治疗进行研究。