Institut Gustave Roussy, Université Paris-Sud, 114 Rue Edouard Vaillant, 94805 Villejuif, France.
Sophia Children's Hospital/Erasmus MC Rotterdam, 60 Dr. Molewaterplein, 3015 GJ Rotterdam, The Netherlands.
Eur J Cancer. 2014 Jan;50(1):170-7. doi: 10.1016/j.ejca.2013.08.012. Epub 2013 Sep 7.
To assess objective response rate (ORR) after two cycles of temozolomide in combination with topotecan (TOTEM) in children with refractory or relapsed neuroblastoma.
This multicenter, non-randomised, phase II study included children with neuroblastoma according to a two-stage Simon design. Eligibility criteria included relapsed or refractory, measurable or metaiodobenzylguanidine (mIBG) evaluable disease, no more than two lines of prior treatment. Temozolomide was administered orally at 150mg/m(2) followed by topotecan at 0.75mg/m(2) intravenously for five consecutive days every 28days. Tumour response was assessed every two cycles according to International Neuroblastoma Response Criteria (INRC), and reviewed independently.
Thirty-eight patients were enroled and treated in 15 European centres with a median age of 5.4years. Partial tumour response after two cycles was observed in 7 out of 38 evaluable patients [ORR 18%, 95% confidence interval (CI) 8-34%]. The best ORR whatever the time of evaluation was 24% (95% CI, 11-40%) with a median response duration of 8.5months. Tumour control rate (complete response (CR)+partial response (PR)+mixed response (MR)+stable disease (SD)) was 68% (95% CI, 63-90%). The 12-months Progression-Free and Overall Survival were 42% and 58% respectively. Among 213 treatment cycles (median 4, range 1-12 per patient) the most common treatment-related toxicities were haematologic. Grade 3/4 neutropenia occurred in 62% of courses in 89% of patients, grade 3/4 thrombocytopenia in 47% of courses in 71% of patients; three patients (8%) had febrile neutropenia.
Temozolomide-Topotecan combination results in very encouraging ORR and tumour control in children with heavily pretreated recurrent and refractory neuroblastoma with favourable toxicity profile.
评估替莫唑胺联合拓扑替康(TOTEM)在复发性或难治性神经母细胞瘤患儿中两个周期后的客观缓解率(ORR)。
这是一项多中心、非随机、Ⅱ期研究,纳入了根据 Simon 两阶段设计的神经母细胞瘤患儿。纳入标准包括复发或难治性、可测量或间碘苄胍(mIBG)可评估疾病、不超过两线既往治疗。替莫唑胺口服 150mg/m2,随后拓扑替康静脉滴注 0.75mg/m2,连续 5 天,每 28 天 1 个周期。根据国际神经母细胞瘤反应标准(INRC)每 2 个周期评估肿瘤反应,并进行独立评估。
38 例患者在 15 个欧洲中心接受治疗,中位年龄为 5.4 岁。38 例可评估患者中有 7 例在两个周期后出现部分肿瘤缓解[ORR 18%,95%置信区间(CI)8-34%]。无论评估时间如何,最佳 ORR 为 24%(95%CI,11-40%),中位缓解持续时间为 8.5 个月。肿瘤控制率(完全缓解(CR)+部分缓解(PR)+混合缓解(MR)+稳定疾病(SD))为 68%(95%CI,63-90%)。12 个月无进展生存率和总生存率分别为 42%和 58%。在 213 个治疗周期(中位数 4 个,范围 1-12 个/患者)中,最常见的治疗相关毒性是血液学毒性。62%的疗程(89%的患者)发生 3/4 级中性粒细胞减少,47%的疗程(71%的患者)发生 3/4 级血小板减少;3 例患者(8%)发生发热性中性粒细胞减少症。
替莫唑胺-拓扑替康联合方案在治疗大量预处理后复发和难治性神经母细胞瘤患儿中,具有非常令人鼓舞的 ORR 和肿瘤控制率,且毒性谱良好。