Wang Li-Hui, Chen Kai, Zhang Na, Yang Jing-Wei, Zhang Ting, Shao Jing-Bo
Department of Hematology/Oncology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200040, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2023 May 15;25(5):476-482. doi: 10.7499/j.issn.1008-8830.2301005.
To investigate the effectiveness of high-dose chemotherapy combined with autologous hematopoietic stem cell transplantation (ASCT) in the treatment of children with high-risk neuroblastoma (NB).
A retrospective analysis was performed on 29 children with high-risk NB who were admitted to Shanghai Children's Hospital and were treated with high-dose chemotherapy combined with ASCT from January 2013 to December 2021, and their clinical features and prognosis were analyzed.
Among the 29 children treated by high-dose chemotherapy combined with ASCT, there were 18 boys (62%) and 11 girls (38%), with a median age of onset of 36 (27, 59) months. According to the International Neuroblastoma Staging System, 6 children (21%) had stage III NB and 23 children (79%) had stage IV NB, and the common metastatic sites at initial diagnosis were bone in 22 children (76%), bone marrow in 21 children (72%), and intracalvarium in 4 children (14%). All 29 children achieved reconstruction of hematopoietic function after ASCT. After being followed up for a median time of 25 (17, 45) months, 21 children (72%) had continuous complete remission and 8 (28%) experienced recurrence. The 3-year overall survival rate and event-free survival rate were 68.9%±16.1% and 61.4%±14.4%, respectively. Presence of bone marrow metastasis, neuron-specific enolase ≥370 ng/mL and positive bone marrow immunophenotyping might reduce the 3-year event-free survival rate (<0.05).
Children with high-risk NB who have bone marrow metastasis at initial diagnosis tend to have a poor prognosis. ASCT combined with high-dose chemotherapy can effectively improve the prognosis of children with NB with a favorable safety profile.
探讨大剂量化疗联合自体造血干细胞移植(ASCT)治疗高危神经母细胞瘤(NB)患儿的疗效。
对2013年1月至2021年12月在上海儿童医学中心收治的29例接受大剂量化疗联合ASCT治疗的高危NB患儿进行回顾性分析,分析其临床特征及预后。
29例接受大剂量化疗联合ASCT治疗的患儿中,男18例(62%),女11例(38%),中位发病年龄为36(27,59)个月。根据国际神经母细胞瘤分期系统,Ⅲ期NB患儿6例(21%),Ⅳ期NB患儿23例(79%),初诊时常见转移部位为骨22例(76%)、骨髓21例(72%)、颅盖内4例(14%)。29例患儿ASCT后均实现造血功能重建。中位随访25(17,45)个月,21例(72%)患儿持续完全缓解,8例(28%)复发。3年总生存率和无事件生存率分别为68.9%±16.1%和61.4%±14.4%。骨髓转移、神经元特异性烯醇化酶≥370 ng/mL及骨髓免疫表型阳性可能降低3年无事件生存率(<0.05)。
初诊时伴有骨髓转移的高危NB患儿预后往往较差。ASCT联合大剂量化疗可有效改善NB患儿预后,安全性良好。