Modak Shakeel, Kushner Brian H, LaQuaglia Michael P, Kramer Kim, Cheung Nai-Kong V
Department of Paediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Eur J Cancer. 2009 Jan;45(1):90-8. doi: 10.1016/j.ejca.2008.09.016. Epub 2008 Nov 6.
The management of patients with International Neuroblastoma Staging System (INSS) stage 3 neuroblastoma (NB) is not consistent worldwide. We describe a single centre approach at Memorial Sloan-Kettering Cancer Centre (MSKCC) from 1991 to 2007 that minimises therapy except for those patients with MYCN-amplified NB.
In this retrospective analysis of 69 patients, tumour MYCN was not amplified in 53 and amplified in 16. Event-free survival (EFS) and overall survival (OS) were determined by Kaplan-Meier analysis.
Fourteen patients with non-MYCN-amplified tumours were treated with surgery alone (group A) and the remaining 39 (group B) with surgery following chemotherapy that was initiated and administered at non-MSKCC institutions. Chemotherapy was discontinued after surgery in 38/39 of the latter. The 10-year EFS and OS for all patients with MYCN-non-amplified NB were 74.9+/-16.9% and 92.6+/-5.5%, respectively. There was no difference in OS between groups A and B (p=0.2; 10-year OS for groups A and B was 84.6+/-14% and 97.1+/-2.9%, respectively). Patients with MYCN-amplified disease (group C) underwent dose-intensive induction, tumour resection and local radiotherapy: 13 achieved complete or very good partial remission, and 10 received myeloablative chemotherapy. 11/16 patients also received 3F8-based immunotherapy: 10 remain free of disease. The 10-year EFS and OS for patients with MYCN-amplified neuroblastoma treated with immunotherapy were both 90.9+/-8.7%.
Patients with MYCN-non-amplified stage 3 NB can be successfully treated with surgery without the need for radiotherapy or continuation of chemotherapy. Combination of dose-intensive chemotherapy, surgery, radiotherapy and immunotherapy was associated with a favourable outcome for most patients with MYCN-amplified stage 3 NB.
国际神经母细胞瘤分期系统(INSS)3期神经母细胞瘤(NB)患者的管理在全球范围内并不一致。我们描述了1991年至2007年纪念斯隆凯特琳癌症中心(MSKCC)的一种单中心方法,该方法将治疗降至最低限度,MYCN扩增的NB患者除外。
在对69例患者的回顾性分析中,53例肿瘤MYCN未扩增,16例扩增。通过Kaplan-Meier分析确定无事件生存期(EFS)和总生存期(OS)。
14例非MYCN扩增肿瘤患者仅接受手术治疗(A组),其余39例(B组)在非MSKCC机构开始并实施化疗后接受手术。后者中38/39例患者术后停止化疗。所有MYCN未扩增NB患者的10年EFS和OS分别为74.9±16.9%和92.6±5.5%。A组和B组的OS无差异(p = 0.2;A组和B组的10年OS分别为84.6±14%和97.1±2.9%)。MYCN扩增疾病患者(C组)接受剂量密集诱导、肿瘤切除和局部放疗:13例实现完全或非常好的部分缓解,10例接受清髓性化疗。11/16例患者还接受了基于3F8的免疫治疗:10例仍无疾病。接受免疫治疗的MYCN扩增神经母细胞瘤患者的10年EFS和OS均为90.9±8.7%。
MYCN未扩增的3期NB患者可通过手术成功治疗,无需放疗或继续化疗。剂量密集化疗、手术、放疗和免疫治疗的联合应用对大多数MYCN扩增的3期NB患者产生了良好的结果。