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儿童高级别胶质瘤——一项波兰多机构研究

High-Grade Gliomas in Children-A Multi-Institutional Polish Study.

作者信息

Napieralska Aleksandra, Krzywon Aleksandra, Mizia-Malarz Agnieszka, Sosna-Zielińska Joanna, Pawłowska Ewa, Krawczyk Małgorzata A, Konat-Bąska Katarzyna, Kaczorowska Aneta, Dąbrowska Anna, Harat Maciej

机构信息

Radiotherapy Department, Maria Sklodowska-Curie National Research Institute of Oncology Gliwice Branch, 44-101 Gliwice, Poland.

Department of Biostatistics and Bioinformatics, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, 44-101 Gliwice, Poland.

出版信息

Cancers (Basel). 2021 Apr 24;13(9):2062. doi: 10.3390/cancers13092062.

DOI:10.3390/cancers13092062
PMID:33923337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8123180/
Abstract

Due to the rarity of high-grade gliomas (HGG) in children, data on this topic are scarce. The study aimed to investigate the long-term results of treatment of children with HGG and to identify factors related to better survival. We performed a retrospective analysis of patients treated for HGG who had the main tumor located outside the brainstem. The evaluation of factors that correlated with better survival was performed with the Cox proportional-hazard model. Survival was estimated with the Kaplan-Meier method. The study group consisted of 82 consecutive patients. All of them underwent surgery as primary treatment. Chemotherapy was applied in 93% of children with one third treated with temozolomide. After or during the systemic treatment, 79% of them received radiotherapy with a median dose of 54 Gy. Median follow-up was 122 months, and during that time, 59 patients died. One-, 2-, 5-, and 10-year overall survival was 78%, 48%, 30% and 17%, respectively. Patients with radical (R0) resection and temozolomide-based chemotherapy had better overall survival. Progression-free survival was better in patients after R0 resection and radical radiotherapy. The best outcome in HGG patients was observed in patients after R0 resection with immediate postoperative temozolomide-based chemotherapy and radical radiotherapy.

摘要

由于儿童高级别胶质瘤(HGG)较为罕见,关于这一主题的数据稀缺。本研究旨在调查HGG患儿的长期治疗结果,并确定与更好生存相关的因素。我们对主要肿瘤位于脑干外的HGG治疗患者进行了回顾性分析。采用Cox比例风险模型对与更好生存相关的因素进行评估。采用Kaplan-Meier法估计生存率。研究组由82例连续患者组成。他们均接受手术作为主要治疗。93%的儿童接受了化疗,其中三分之一接受替莫唑胺治疗。在全身治疗后或治疗期间,79%的患者接受了放疗,中位剂量为54 Gy。中位随访时间为122个月,在此期间,59例患者死亡。1年、2年、5年和10年总生存率分别为78%、48%、30%和17%。接受根治性(R0)切除和基于替莫唑胺化疗的患者总生存率更高。R0切除和根治性放疗后的患者无进展生存期更好。HGG患者中,R0切除后立即接受基于替莫唑胺的化疗和根治性放疗的患者预后最佳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/184b/8123180/a0e03e100a15/cancers-13-02062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/184b/8123180/79a06bcd5c2e/cancers-13-02062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/184b/8123180/a0e03e100a15/cancers-13-02062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/184b/8123180/79a06bcd5c2e/cancers-13-02062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/184b/8123180/a0e03e100a15/cancers-13-02062-g002.jpg

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Neuro Oncol. 2019 Nov 1;21(Suppl 5):v1-v100. doi: 10.1093/neuonc/noz150.
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Clinical outcome and molecular characterization of pediatric glioblastoma treated with postoperative radiotherapy with concurrent and adjuvant temozolomide: a single institutional study of 66 children.
多次鞘内注射同种异体自然杀伤细胞在难治性/复发性小儿脑肿瘤中的安全性和可行性。
BMC Cancer. 2025 May 27;25(1):952. doi: 10.1186/s12885-025-14314-6.
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Therapeutically targeting the unique disease landscape of pediatric high-grade gliomas.针对小儿高级别胶质瘤独特疾病格局的治疗靶点。
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