儿童神经母细胞瘤肿瘤倍性与总生存率的关系。

Puerto Rico health sciences journal Pub Date : 2025-03-01
Tyrel R Porter, Emir Rinaldi-Pérez, Marcel Grau-Rodríguez, Lilia Y Kucheryavykh
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摘要

目的:探讨小儿神经母细胞瘤预后、肿瘤倍性和种族之间的关系,重点关注总生存期(OS)的差异,同时考虑种族和民族因素。方法:从cBioPortal for Cancer Genomics (TARGET [Therapeutically applied Research to Generate Effective therapies], 2018)获取63名西班牙裔白人、561名非西班牙裔白人和86名非西班牙裔黑人患者的临床和肿瘤倍体数据。Kaplan Meier生存曲线分析采用log-rank检验和Gehan-Breslow Wilcoxon检验。采用Mantel-Haenszel方法计算95% ci的风险比(HR)。使用卡方检验评估种族与肿瘤倍性之间的关系。结果:在自认为是西班牙裔的白人患者和自认为是非西班牙裔的白人患者之间观察到总生存期(OS)的显著差异,其中西班牙裔患者表现出更差的预后。(p = 0.0076, hr = 1.907, 95% ci: 1.187-3.062)。西班牙裔患者的中位生存期为94个月,但非西班牙裔患者的中位生存期不确定。二倍体肿瘤的预后比超二倍体肿瘤差(P < 0.0001, HR = 2.291, 95% CI: 1.689-3.109)。卡方检验显示,种族与肿瘤倍性之间存在显著相关性(χ2 = 4.220, P = 0.0400),非西班牙裔患者患超二倍体肿瘤的比例(66.99%)高于西班牙裔患者(53.97%)。结论:西班牙裔白人神经母细胞瘤患者的OS低于非西班牙裔白人患者,部分原因是前者具有更高比例的二倍体肿瘤。这些发现强调了在风险分层和治疗策略中考虑种族和肿瘤倍性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between Tumor Ploidy and Overall Survival in Pediatric Neuroblastoma.

Objective: To investigate the relationships between pediatric neuroblastoma outcomes, tumor ploidy, and ethnicity, focusing on disparities in overall survival (OS) while also accounting for race and ethnicity.

Methods: Clinical and tumor ploidy data for 63 Hispanic White, 561 non-Hispanic White, and 86 non-Hispanic Black patients were obtained from cBioPortal for Cancer Genomics (TARGET [Therapeutically Applicable Research to Generate Effective Treatments], 2018). Kaplan Meier survival curves were analyzed using log-rank and Gehan-Breslow Wilcoxon tests. Hazard ratios (HR) with 95% CIs were calculated using the Mantel-Haenszel method. Associations between ethnicity and tumor ploidy were assessed using the chi-square test.

Results: Significant differences in overall survival (OS) were observed between White patients who self-identified as Hispanic and those who identified as non Hispanic, with Hispanic patients exhibiting worse outcomes. (P = .0076, HR = 1.907, 95% CI: 1.187-3.062). Median survival for Hispanic patients was 94 months but was undefined for non-Hispanic patients. Diploid tumors were associated with worse outcomes than hyperdiploid tumors were (P < .0001, HR = 2.291, 95% CI: 1.689-3.109). The chi square test revealed a significant association between ethnicity and tumor ploidy (χ2 = 4.220, P = .0400), with non-Hispanic patients having a higher proportion of hyperdiploid tumors (66.99%) than Hispanic patients (53.97%).

Conclusion: Hispanic White patients with neuroblastoma had lower OS than did non-Hispanic White patients, partly due to the former having a higher proportion of diploid tumors. These findings highlight the importance of considering ethnicity and tumor ploidy in risk stratification and treatment strategies.

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