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[Effectiveness of autologous hematopoietic stem cell transplantation in the treatment of high-risk neuroblastoma in children: a single-center clinical study].[自体造血干细胞移植治疗儿童高危神经母细胞瘤的疗效:一项单中心临床研究]
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本文引用的文献

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Retrospective Analysis of INRG Clinical and Genomic Factors for 605 Neuroblastomas in Japan: A Report from the Japan Children's Cancer Group Neuroblastoma Committee (JCCG-JNBSG).日本儿童癌症集团神经母细胞瘤委员会(JCCG-JNBSG)对 605 例神经母细胞瘤的 INRG 临床和基因组因素的回顾性分析
Biomolecules. 2021 Dec 23;12(1):18. doi: 10.3390/biom12010018.
2
Factors of Recurrence After Complete Response in Children with Neuroblastoma: A 16-Year Retrospective Study of 179 Cases.神经母细胞瘤患儿完全缓解后的复发因素:一项对179例病例的16年回顾性研究
Cancer Manag Res. 2022 Jan 6;14:107-122. doi: 10.2147/CMAR.S343648. eCollection 2022.
3
Autologous or allogeneic hematopoietic stem cells transplantation combined with high-dose chemotherapy for refractory neuroblastoma: A protocol for systematic review and meta-analysis.自体或同种异体造血干细胞移植联合大剂量化疗治疗难治性神经母细胞瘤:系统评价和荟萃分析方案。
Medicine (Baltimore). 2021 Dec 10;100(49):e28096. doi: 10.1097/MD.0000000000028096.
4
Pediatric high risk neuroblastoma with autologous stem cell transplant - 20 years of experience.小儿高危神经母细胞瘤自体干细胞移植——20年经验
Int J Pediatr Adolesc Med. 2021 Dec;8(4):253-257. doi: 10.1016/j.ijpam.2021.02.006. Epub 2021 Mar 3.
5
Clinical and molecular characterization of patients with stage 4(M) neuroblastoma aged less than 18 months without MYCN amplification.18 个月以下无 MYCN 扩增的 4 期(M)神经母细胞瘤患者的临床和分子特征。
Pediatr Blood Cancer. 2021 Aug;68(8):e29038. doi: 10.1002/pbc.29038. Epub 2021 Apr 7.
6
Biological features and clinical outcome in infant neuroblastoma: a multicenter experience in Beijing.婴儿神经母细胞瘤的生物学特征和临床结局:北京的一项多中心经验。
Eur J Pediatr. 2021 Jul;180(7):2055-2063. doi: 10.1007/s00431-021-03989-1. Epub 2021 Feb 13.
7
Immunotherapy approaches targeting neuroblastoma.免疫疗法靶向治疗神经母细胞瘤。
Curr Opin Pediatr. 2021 Feb 1;33(1):19-25. doi: 10.1097/MOP.0000000000000982.
8
Long-term follow-up of children with neuroblastoma receiving radiotherapy to metastatic lesions within the German Neuroblastoma Trials NB97 and NB 2004.神经母细胞瘤试验 NB97 和 NB2004 中接受放疗治疗转移病灶的神经母细胞瘤患儿的长期随访。
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[Clinical characteristics and prognostic analysis of 458 children with high-risk neuroblastoma in a single center].单中心458例高危神经母细胞瘤患儿的临床特征及预后分析
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[联合治疗对4期神经母细胞瘤患儿的临床疗效]

[Clinical efficacy of combined therapy in children with stage 4 neuroblastoma].

作者信息

Liang Wei-Ling, Ye Xiao-Fan, Zhong Gong, Chen Jian-Jun, Dai Kang-Lin, Cheuk Ka Leung Daniel, Mo Shu, Wang Bo-Shen, Li Chun-Yu, Jiang Xuan-Zhu, Xu Zhi-Yuan, Zhou Li, Chan Irene, Chen Jian-Liang, Chu Patrick, Lee Pui Wah Pamela, Chan Chi Fung Godfrey

机构信息

Department of Pediatrics, Hong Kong University-Shenzhen Hospital, Shenzhen, Guangdong 518000, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2022 Jul 15;24(7):759-764. doi: 10.7499/j.issn.1008-8830.2203049.

DOI:10.7499/j.issn.1008-8830.2203049
PMID:35894190
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9336616/
Abstract

OBJECTIVES

To study the early clinical efficacy of combined therapy of stage 4 neuroblastoma.

METHODS

A retrospective analysis was performed on the medical data and follow-up data of 14 children with stage 4 neuroblastoma who were diagnosed in Hong Kong University-Shenzhen Hospital from January 2016 to June 2021.

RESULTS

The median age of onset was 3 years and 7.5 months in these 14 children. Among these children, 9 had positive results of bone marrow biopsy, 4 had - gene amplification, 13 had an increase in neuron-specific enolase, and 7 had an increase in vanilmandelic acid in urine. Based on the results of pathological examination, differentiated type was observed in 6 children, undifferentiated type in one child, mixed type, in one child and poorly differentiated type in 6 children. Of all the children, 10 received chemotherapy with the N7 regimen (including 2 children receiving arsenic trioxide in addition) and 4 received chemotherapy with the Rapid COJEC regimen. Thirteen children underwent surgery, 14 received hematopoietic stem cell transplantation, and 10 received radiotherapy. A total of 8 children received Ch14.18/CHO immunotherapy, among whom 1 child discontinued due to anaphylactic shock during immunotherapy, and the other 7 children completed Ch14.18/CHO treatment without serious adverse events, among whom 1 child was treated with Lu177 Dotatate 3 times after recurrence and is still undergoing chemotherapy at present. The median follow-up time was 45 months for all the 14 children. Four children experienced recurrence within 2 years, and the 2-year overall survival rate was 100%; 4 children experienced recurrence within 3 years, and 7 achieved disease-free survival within 3 years.

CONCLUSIONS

Multidisciplinary combined therapy is recommended for children with stage 4 neuroblastoma and can help them achieve better survival and prognosis.

摘要

目的

研究4期神经母细胞瘤联合治疗的早期临床疗效。

方法

对2016年1月至2021年6月在香港大学深圳医院确诊的14例4期神经母细胞瘤患儿的医疗数据和随访数据进行回顾性分析。

结果

这14例患儿的中位发病年龄为3岁7.5个月。其中,9例骨髓活检结果为阳性,4例有 - 基因扩增,13例神经元特异性烯醇化酶升高,7例尿香草扁桃酸升高。根据病理检查结果,6例患儿为分化型,1例为未分化型,1例为混合型,6例为低分化型。所有患儿中,10例接受N7方案化疗(其中2例加用三氧化二砷),4例接受Rapid COJEC方案化疗。13例患儿接受了手术,14例接受了造血干细胞移植,10例接受了放疗。共有8例患儿接受了Ch14.18/CHO免疫治疗,其中1例在免疫治疗期间因过敏性休克停药,其他7例完成Ch14.18/CHO治疗且无严重不良事件,其中1例复发后接受了3次Lu177 Dotatate治疗,目前仍在接受化疗。14例患儿的中位随访时间为45个月。4例患儿在2年内复发,2年总生存率为100%;4例患儿在3年内复发,7例患儿在3年内无病生存。

结论

推荐对4期神经母细胞瘤患儿采用多学科联合治疗,有助于其获得更好的生存和预后。