临床儿科杂志 ›› 2023, Vol. 41 ›› Issue (9): 686-691.doi: 10.12372/jcp.2023.22e1634

• 综合报道 • 上一篇    下一篇

G4型髓母细胞瘤患儿预后影响因素及生存状况分析

武跃芳, 孙艳玲(), 武万水, 杜淑旭, 李苗, 孙黎明   

  1. 首都医科大学附属世纪坛医院(北京 100038)
  • 收稿日期:2022-12-06 出版日期:2023-09-15 发布日期:2023-09-05
  • 通讯作者: 孙艳玲 E-mail:sunyanling@bjsjth.cn

Analysis of prognostic factors and survival status of group 4 medulloblastoma in children

WU Yuefang, SUN Yanling(), WU Wanshui, DU Shuxu, LI Miao, SUN Liming   

  1. Department of Pediatrics, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China
  • Received:2022-12-06 Online:2023-09-15 Published:2023-09-05
  • Contact: SUN Yanling E-mail:sunyanling@bjsjth.cn

摘要:

目的 探讨儿童G4型髓母细胞瘤(MB)患者的生存状况及其预后影响因素。方法 回顾性分析2016年5月至2020年8月儿科收治的G4型MB患儿(随访至2022年8月)的临床资料,采用Kaplan-Meier法计算总体生存(OS)率和无进展生存(PFS)率,采用Log-rank检验比较组间生存率差异,采用Cox回归模型分析影响预后的因素。结果 纳入145例G4型MB患儿,男106例、女39例,中位确诊年龄7.5(5.7~9.6)岁。M0期91例,M+期54例(M1期1例、M2期12例、M3期41例);病理分型为经典型127例、促纤维增生/结节型(DN)8例、大细胞/间变型(LC/A)8例、广泛结节型(EN)1例、未分型1例。中位随访时间为47.9(36.5~59.3)月,复发37例。患儿5年OS率和PFS率分别为(80.8±3.4)%和(55.4±4.7)%。Cox回归分析结果提示M+期、MYCN扩增、Chr12 p+变异是影响预后的独立危险因素(P<0.05)。结论 M+期、MYCN扩增的G4型MB患儿预后相对较差。Chr12 p+可能与患儿预后相关,但仍有待更大样本的临床研究进行证实。

关键词: G4型髓母细胞瘤, 预后, 影响因素, 儿童

Abstract:

Objective To investigate the survival status and prognostic factors of group 4 medulloblastoma (MB) in children. Methods The clinical data of children with group 4 MB admitted to the Department of Pediatrics from May 2016 to August 2020 (follow-up until August 2022) were retrospectively analyzed. The Kaplan-Meier method was used to calculate the overall survival (OS) rate and progression-free survival (PFS) rate. Log-rank test was used to compare the difference in survival rate between groups, and Cox regression model was used to analyze the factors affecting prognosis. Results A total of 145 children (106 boys and 39 girls) with group 4 MB were included, and the median age of diagnosis was 7.5 (5.7-9.6) years old. There were 91 children in M0 stage and 54 children in M+ stage (1 in M1 stage, 12 in M2 stage and 41 in M3 stage). The pathologic types were classic in 127 cases, desmoplastic/nodular (DN) in 8 cases, anaplastic/large cell (LC/A) in 8 cases, extensive nodularity (EN) in 1 case, and none of somatotype (NOS) in 1 case. The median follow-up time was 47.9 (36.5-59.3) months, and 37 children had tumor recurrence. The 5-year OS and PFS rates were (80.8±3.4) % and (55.4±4.7) %, respectively. Cox regression analysis indicated that M+ stage, MYCN amplification and Chr12p+ variation were independent risk factors for prognosis (P<0.05). Conclusions Group 4 MB children with M+ stage or MYCN amplification have a relatively poor prognosis. Chr12p + may be related to the prognosis of children, but it needs to be confirmed by clinical studies with larger samples.

Key words: group 4 medulloblastoma, prognosis, influencing factor, child