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骨外尤文肉瘤的临床人口统计学特征:儿童和成人患者的比较荟萃分析

Clinicodemographic characteristics of extraosseous ewing sarcoma: A comparative meta-analysis of pediatric and adult patients.

作者信息

Ghandour Maher, Semaan Karl, Saad Eddy, Horsch Axel, Abdallah Ralph, Semaan Doumit

机构信息

Orthopedics Department, Heidelberg University Hospital, Germany.

Orthopedics Department, Lebanese University, Lebanon.

出版信息

J Orthop. 2023 Sep 9;44:86-92. doi: 10.1016/j.jor.2023.09.002. eCollection 2023 Oct.

DOI:10.1016/j.jor.2023.09.002
PMID:37731676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10507075/
Abstract

BACKGROUND

Evidence suggests different presentation patterns and prognosis of extraosseous Ewing Sarcoma (EES) based on age. Thus, we carried out this study to test the difference between children and adult EES cases regarding clinicodemographic characteristics and prognosis.

METHODS

A total of 4 databases were explored yielding 18 relevant studies for data synthesis. Outcomes included the comparison of demographic and clinical characteristics as well as prognosis between children and adults with EES. Log odds ratio (logOR) and its 95% confidence interval (CI) were pooled across studies. Statistical models/methods were selected based on heterogeneity.

RESULTS

Our analysis included a total of 1261 children and 1256 adults. When we compared these two age categories, we did not observe a significant difference in the risk of developing EES [logOR = -0.13; 95% CI: -0.65: 0.39; I2 = 88.42%]. No significant differences regarding gender, tumor location, and size (≤5 vs. >5 cm), EWSR1 positivity, or management modality. We did not observe significant difference regarding clinical outcomes, such as 5-year overall survival and event-free survival, recurrence, mortality, no evidence of disease, and secondary metastasis.

CONCLUSIONS

Our findings highlight the absence of an association between the age category of patients and the incidence of EES, as well as its clinical outcomes.

摘要

背景

有证据表明,骨外尤文肉瘤(EES)的表现模式和预后因年龄而异。因此,我们开展了这项研究,以检验儿童和成人EES病例在临床人口统计学特征和预后方面的差异。

方法

共检索了4个数据库,得到18项相关研究用于数据合成。结果包括对EES儿童和成人的人口统计学和临床特征以及预后进行比较。对各研究的对数比值比(logOR)及其95%置信区间(CI)进行合并。根据异质性选择统计模型/方法。

结果

我们的分析共纳入了1261名儿童和1256名成人。当我们比较这两个年龄组时,未观察到发生EES风险的显著差异[logOR = -0.13;95% CI:-0.65:0.39;I2 = 88.42%]。在性别、肿瘤位置和大小(≤5 vs.>5 cm)、EWSR1阳性或治疗方式方面无显著差异。我们未观察到临床结局方面的显著差异,如5年总生存率和无事件生存率、复发、死亡率、无疾病证据和继发转移。

结论

我们的研究结果表明,患者年龄类别与EES的发病率及其临床结局之间不存在关联。

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Children (Basel). 2022 Nov 29;9(12):1859. doi: 10.3390/children9121859.
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Extraosseous Ewing sarcoma in children and adolescents: A retrospective series from a referral pediatric oncology center.儿童和青少年骨外尤文肉瘤:来自一家儿科肿瘤转诊中心的回顾性系列研究。
Pediatr Blood Cancer. 2022 May;69(5):e29512. doi: 10.1002/pbc.29512. Epub 2021 Dec 28.
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Incidence and Demographic Profile of Ewings Sarcoma: Experience From a Tertiary Care Hospital.尤因肉瘤的发病率及人口统计学特征:来自一家三级护理医院的经验
Cureus. 2021 Sep 28;13(9):e18339. doi: 10.7759/cureus.18339. eCollection 2021 Sep.
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Primary Ewing's sarcoma with orbit involvement: Survival and visual outcomes after eye-sparing multidisciplinary management in eight patients.原发性尤文肉瘤累及眼眶:8 例患者行保眼多学科综合治疗后的生存和视力结局。
Head Neck. 2021 Dec;43(12):3857-3865. doi: 10.1002/hed.26884. Epub 2021 Oct 10.
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Extraskeletal Ewing sarcoma in children, adolescents, and young adults. An analysis of three prospective studies of the Cooperative Weichteilsarkomstudiengruppe (CWS).儿童、青少年和青年的骨外尤文肉瘤。合作软组织肉瘤研究组(CWS)三项前瞻性研究的分析。
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