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不可切除的局限性神经母细胞瘤:含卡铂-依托泊苷的初始化疗后生存率提高。法国儿科肿瘤学会(SFOP)神经母细胞瘤研究组

Unresectable localized neuroblastoma: improved survival after primary chemotherapy including carboplatin-etoposide. Neuroblastoma Study Group of the Société Française d'Oncologie Pédiatrique (SFOP).

作者信息

Rubie H, Michon J, Plantaz D, Peyroulet M C, Coze C, Frappaz D, Chastagner P, Baranzelli M C, Méchinaud F, Boutard P, Lutz P, Perel Y, Leverger G, de Lumley L, Millot F, Stéphan J L, Margueritte G, Hartmann O

机构信息

Unité d' Hémato-Oncologie Pédiatrique, Service de Médecine Infantile B, CHU Purpan, Toulouse, France.

出版信息

Br J Cancer. 1998 Jun;77(12):2310-7. doi: 10.1038/bjc.1998.384.

Abstract

Neuroblastomas (NBs) were assessed according to INSS recommendations including MIBG scan and extensive bone marrow staging to eliminate metastatic spread. Patients with unresectable tumour received primary chemotherapy including two courses of carboplatin-etoposide (CE) and two of vincristine-cyclophosphamide-doxorubicin (CAdO). Post-operative treatment was to be given only in children over 1 year of age at diagnosis who had residual disease or lymph node (LN) involvement. Between 1990 and 1994, 130 consecutive children were registered. In comparison with resectable primaries, these tumours were more commonly abdominal, larger and associated with N-myc amplification (NMA). Complete, very good and partial response (CR, VGPR, PR) to CE were, respectively, 1%, 7% and 44%, overall response rate (RR) to two courses of CE and two courses of CAdO was 71%, and the tumour could be removed in all but four of the children. The toxicity was manageable. The 5-year overall survival (OS) and event-free survival (EFS) were, respectively, 88% and 78% with a median follow-up of 38 months. In multivariate analysis, only NMA and LN involvement adversely influenced the outcome, particularly NMA. Children with unresectable NBs and no NMA fared as well as children with resectable ones as OS were, respectively, 95% and 99% and EFS 89% and 91%. Our data show encouraging results in localized but unresectable NBs as 90% of children may be considered as definitely cured, especially those without NMA.

摘要

根据国际神经母细胞瘤分期系统(INSS)的建议对神经母细胞瘤(NBs)进行评估,包括间碘苄胍(MIBG)扫描和广泛的骨髓分期,以排除转移扩散。无法切除肿瘤的患者接受一线化疗,包括两个疗程的卡铂-依托泊苷(CE)和两个疗程的长春新碱-环磷酰胺-阿霉素(CAdO)。仅对诊断时年龄超过1岁且有残留疾病或淋巴结(LN)受累的儿童进行术后治疗。1990年至1994年,连续登记了130名儿童。与可切除的原发性肿瘤相比,这些肿瘤更常见于腹部,体积更大且与N-myc扩增(NMA)相关。对CE的完全缓解、非常好的缓解和部分缓解(CR、VGPR、PR)分别为1%、7%和44%,对两个疗程的CE和两个疗程的CAdO的总缓解率(RR)为71%,除4名儿童外,所有儿童的肿瘤均可切除。毒性可控。5年总生存率(OS)和无事件生存率(EFS)分别为88%和78%,中位随访时间为38个月。多变量分析显示,只有NMA和LN受累对预后有不利影响,尤其是NMA。无法切除且无NMA的NBs儿童与可切除的儿童预后相似,OS分别为95%和99%,EFS分别为89%和91%。我们的数据显示,局部但无法切除的NBs取得了令人鼓舞的结果,因为90%的儿童可被视为已完全治愈,尤其是那些无NMA的儿童。

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