Poverty, race, ethnicity, and survival in pediatric nonmetastatic osteosarcoma: a Children's Oncology Group report.

IF 9.9 1区 医学 Q1 ONCOLOGY JNCI Journal of the National Cancer Institute Pub Date : 2024-10-01 DOI:10.1093/jnci/djae103
Lenka Ilcisin, Ruxu Han, Mark Krailo, David S Shulman, Brent R Weil, Christopher B Weldon, Puja Umaretiya, Rahela Aziz-Bose, Katie A Greenzang, Richard Gorlick, Damon R Reed, R Lor Randall, Helen Nadel, Odion Binitie, Steven G Dubois, Katherine A Janeway, Kira Bona
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Abstract

Background: Children living in poverty and those of marginalized race or ethnicity experience inferior disease outcomes across many cancers. Whether survival disparities exist in osteosarcoma is poorly defined. We investigated the association between race, ethnicity, and proxied poverty exposures and event-free and overall survival for children with nonmetastatic osteosarcoma receiving care on a cooperative group trial.

Methods: We conducted a retrospective cohort study of US patients with nonmetastatic, osteosarcoma aged 5-21 years enrolled on the Children's Oncology Group trial AOST0331. Race and ethnicity were categorized to reflect historically marginalized populations, as Hispanic, non-Hispanic Black, non-Hispanic Other, and non-Hispanic White. Poverty was proxied at the household and neighborhood levels. Overall survival and event-free survival functions of time from trial enrollment were estimated using the Kaplan-Meier method. Hypotheses of associations between risks for event-free survival, death, and postrelapse death with race and ethnicity were assessed using log-rank tests.

Results: Among 758 patients, 25.6% were household-poverty and 28.5% neighborhood-poverty exposed. Of the patients, 21% of children identified as Hispanic, 15.4% non-Hispanic Black, 5.3% non-Hispanic Other, and 54.0% non-Hispanic White. Neither household or neighborhood poverty nor race and ethnicity were statistically significantly associated with risks for event-free survival or death. Postrelapse risk for death differed statistically significantly across race and ethnicity with non-Hispanic Black patients at greatest risk (4-year postrelapse survival 35.7% Hispanic vs 13.0% non-Hispanic Black vs 43.8% non-Hispanic Other vs 38.9% non-Hispanic White; P = .0046).

Conclusions: Neither proxied poverty exposures or race and ethnicity were associated with event-free survival or overall survival, suggesting equitable outcomes following frontline osteosarcoma trial-delivered therapy. Non-Hispanic Black children experienced statistically significant inferior postrelapse survival. Investigation of mechanisms underlying postrelapse disparities are paramount.

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贫困、种族、民族与小儿非转移性骨肉瘤的存活率:儿童肿瘤学组报告。
背景:在许多癌症中,贫困儿童和边缘化种族或族裔儿童的疾病预后较差。骨肉瘤的存活率是否存在差异,目前尚不明确。我们调查了在合作小组试验中接受治疗的非转移性骨肉瘤患儿的种族、民族和替代贫困暴露与无事件生存率和总生存率之间的关系:我们对参加儿童肿瘤集团 AOST0331 试验的 5-21 岁美国非转移性骨肉瘤患者进行了一项回顾性队列研究。为了反映历史上被边缘化的人群,对种族和民族进行了分类,包括西班牙裔、非西班牙裔黑人、非西班牙裔其他族裔和非西班牙裔白人。贫困以家庭和邻里为单位。使用 Kaplan-Meier 方法估算了试验入组时间的总生存率和无事件生存率。使用对数秩检验评估了无事件生存、死亡和复发后死亡风险与种族和民族之间的假设关系:在 758 名患者中,25.6% 属于家庭贫困,28.5% 属于邻里贫困。在患者中,21%的儿童被认定为西班牙裔,15.4%为非西班牙裔黑人,5.3%为非西班牙裔其他,54.0%为非西班牙裔白人。从统计学角度看,家庭或邻里贫困以及种族和民族与无事件生存或死亡风险均无明显关联。不同种族和族裔的患者复发后的死亡风险在统计学上有显著差异,其中非西班牙裔黑人患者的风险最大(复发后4年生存率为35.7%西班牙裔 vs 13.0% 非西班牙裔黑人 vs 43.8% 非西班牙裔其他族裔 vs 38.9% 非西班牙裔白人;P = .0046):结论:贫困替代暴露或种族和民族均与无事件生存期或总生存期无关,这表明骨肉瘤前线试验提供的治疗结果是公平的。非西班牙裔黑人儿童的复发后存活率在统计学上明显较低。调查导致复发后差异的机制至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.00
自引率
2.90%
发文量
203
审稿时长
4-8 weeks
期刊介绍: The Journal of the National Cancer Institute is a reputable publication that undergoes a peer-review process. It is available in both print (ISSN: 0027-8874) and online (ISSN: 1460-2105) formats, with 12 issues released annually. The journal's primary aim is to disseminate innovative and important discoveries in the field of cancer research, with specific emphasis on clinical, epidemiologic, behavioral, and health outcomes studies. Authors are encouraged to submit reviews, minireviews, and commentaries. The journal ensures that submitted manuscripts undergo a rigorous and expedited review to publish scientifically and medically significant findings in a timely manner.
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