Department of Paediatric Oncology, Southampton General Hospital, Southampton, UK.
Eur J Cancer. 2013 Nov;49(17):3671-9. doi: 10.1016/j.ejca.2013.07.002. Epub 2013 Jul 29.
In children older than 1 year with localised unresectable neuroblastoma (NB), treatment strategies are heterogeneous according to the national groups. The objective of this phase III non-randomised study was to evaluate the efficacy of conventional chemotherapy followed by surgery.
In the presence of surgical risk factors (SRF), six courses of chemotherapy alternating Carboplatin-Etoposide and Vincristin-Cyclophosphamide-Doxorubicin were given, and surgical resection was attempted after four. Survival analyses were performed using an intention-to-treat approach. The main objective was to achieve a 5-year survival over 80%.
Out of 191 registered children, 160 were evaluable. There were 62.5% older than 18 months and 52.5% had unfavourable histology according to International Neuroblastoma Pathology Classification (INPC). Chemotherapy reduced the number of SRFs by one third. Delayed surgery was attempted in 86.3% of patients and was complete or nearly complete in 74%. The 5-year EFS and OS were 76.4% and 87.6% respectively, with significant better results for patients younger than 18 months or with favourable histology.
This strategy provides encouraging results in children older than 1 year or 12 months with localised unresectable NB without MYCN amplification. However, in children older than 18 months and with unfavourable histology, additional treatment is recommended.
对于 1 岁以上局部不可切除神经母细胞瘤(NB)的儿童,治疗策略因国家组别而异。本 III 期非随机研究的目的是评估先化疗后手术的疗效。
存在手术风险因素(SRF)时,给予六周期卡铂依托泊苷和长春新碱环磷酰胺多柔比星交替化疗,并在四个周期后尝试手术切除。采用意向治疗方法进行生存分析。主要目标是实现 80%以上的 5 年生存率。
191 名登记的患儿中,160 名可评估。62.5%的患儿年龄大于 18 个月,52.5%的患儿根据国际神经母细胞瘤病理学分类(INPC)具有不良组织学特征。化疗使 SRF 的数量减少了三分之一。86.3%的患儿尝试了延迟手术,其中 74%的患儿手术完全或几乎完全切除。5 年 EFS 和 OS 分别为 76.4%和 87.6%,年龄小于 18 个月或组织学良好的患儿结果显著更好。
对于无 MYCN 扩增的局部不可切除 NB 患儿,1 岁以上或 12 个月以上的患儿,这种策略提供了令人鼓舞的结果。然而,对于年龄大于 18 个月和组织学不良的患儿,建议进行额外的治疗。