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评估儿童肿瘤学组(COG)2004-2015 年直接治疗临床试验的入组特征。

Assessment of enrollment characteristics for Children's Oncology Group (COG) upfront therapeutic clinical trials 2004-2015.

机构信息

Center for Cancer and Blood Disorders, Department of Pediatrics, School of Medicine and Children's Hospital Colorado, University of Colorado Aurora, CO, United States of America.

University of Colorado Comprehensive Cancer Center, Aurora, CO, United States of America.

出版信息

PLoS One. 2020 Apr 23;15(4):e0230824. doi: 10.1371/journal.pone.0230824. eCollection 2020.

Abstract

BACKGROUND

Improvements in pediatric cancer survival are attributed to cooperative clinical trials. Under-representation of specific demographic groups has been described in adult and pediatric cancer trials and poses a threat to the generalizability of results. An evaluation of data provided by the Children's Oncology Group (COG) of upfront trial enrollment for US patients 0 to 29 years old between 2004 and 2015 was performed.

METHODS

US cancer cases were estimated using incidence data and US population estimates from the Surveillance, Epidemiology, and End Results Program and compared to observed COG cases. Percent enrollment and standardized ratios of enrollment were calculated across demographic, disease, and socioeconomic groups. The COG website was utilized to quantify available trials and assess age eligibility.

RESULTS

19.9% of estimated US cancer patients age 0 to 19 years enrolled on COG trials. Younger patients were more represented across diseases and races/ethnicities. Patients with hematologic malignancies were more represented compared to solid and central nervous system (CNS) tumors.

CONCLUSION

COG trial enrollment rates are declining when compared to previously published data, potentially from challenges in pediatric drug development, difficulty designing feasible trials for highly curable diagnoses, and issues ensuring trial availability for the heterogeneous group of solid and CNS tumors. Though racial/ethnic groups and county-level socioeconomic factors were proportionally represented, under representation of the adolescent/young adult (AYA) population and younger patients with solid and CNS tumors remains a concern. Targeted efforts should focus on these subgroups and further research should evaluate AYA enrollment rates across all available trials.

摘要

背景

儿科癌症存活率的提高归因于合作临床试验。在成人和儿科癌症试验中,特定人群的代表性不足已被描述,这对结果的普遍性构成了威胁。对 2004 年至 2015 年期间儿童肿瘤学组(COG)为美国 0 至 29 岁患者提供的初步试验登记数据进行了评估。

方法

利用发病率数据和监测、流行病学和最终结果计划中的美国人口估计数来估计美国癌症病例,并将其与观察到的 COG 病例进行比较。按人口统计学、疾病和社会经济群体计算登记的百分比和标准化登记比率。利用 COG 网站来量化可用的试验并评估年龄资格。

结果

估计年龄在 0 至 19 岁的美国癌症患者中有 19.9%参加了 COG 试验。在各种疾病和种族/族裔中,年轻患者的代表性更高。与实体瘤和中枢神经系统(CNS)肿瘤相比,血液恶性肿瘤患者的代表性更高。

结论

与之前发表的数据相比,COG 试验登记率正在下降,这可能是由于儿科药物开发的挑战、为高度可治愈的诊断设计可行试验的困难以及确保异构的实体瘤和 CNS 肿瘤的试验可用性的问题。尽管种族/族裔群体和县级社会经济因素的比例适当,但青少年/年轻成人(AYA)人群和年龄较小的实体瘤和 CNS 肿瘤患者的代表性不足仍然令人担忧。有针对性的努力应集中在这些亚组上,进一步的研究应评估所有可用试验中的 AYA 登记率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/7179840/22641b13f2d0/pone.0230824.g001.jpg

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