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2012年至2021年美国食品药品监督管理局新型肿瘤治疗药物批准的关键试验中女性、老年人以及少数族裔患者的代表性:亮点试验及随时间的趋势

Representation of Women, Older Adults, and Racial and Ethnic Minoritized Patients in Pivotal Trials for US Food and Drug Administration Novel Oncology Therapeutic Approvals, 2012-2021: Bright Spot Trials and Trends Over Time.

作者信息

Miller Jennifer E, Pelletiers William, Gross Cary P, Mello Michelle, Ramachandran Reshma, Schwartz Jason L, Suttiratana Sakinah Carter, Varma Tanvee, Ross Joseph S

机构信息

Section of General Internal Medicine, Yale School of Medicine, New Haven, CT.

Equity Research and Innovation Center, Yale School of Medicine, New Haven, CT.

出版信息

JCO Oncol Pract. 2025 Jun 10:OP2400563. doi: 10.1200/OP-24-00563.

Abstract

PURPOSE

To examine trends over time in clinical trial diversity for oncology therapeutics, identify bright spot trials adequately representing Black or Latino patients, and examine their associations with trial characteristics.

METHODS

This retrospective cross-sectional study of trials supporting US Food and Drug Administration (FDA) oncology therapeutic approvals (2012-2021) compared proportions of enrolled women, older adults, and racial and ethnic minoritized patients with US patient populations with approved indications and US census data, exploring trends over time. We estimated the likelihood that an organization sponsoring a trial adequately representing Black patients also sponsored a trial adequately representing Latino patients, and vice versa, and examined associations of bright spot trials, trials adequately representing Black or Latino patients, with trial characteristics.

RESULTS

The FDA approved 111 oncology therapeutics (2012-2021) from 70 sponsors, on 121 trials enrolling 50,871 patients, of which 22,155 (44%) were women, 9,442 (19%) older adults (>64 years), 5,319 (9.6%) Asian, 1,353 (3%) Black, and 1,511 (3%) Latino. Zero trials adequately represented all patient demographics with no improvements for any group over the past 10 years ( values >.05), and 80% adequately represented women, 44% older adults (>64 years), and 2% racial and ethnic minoritized patients. We identified 33 bright spot trials, the likelihood of which was associated with individual sponsors ( < .0001), but not sponsor size ( = .22), indication ( = .20), or trial phase ( = .32). There were no associations between a company sponsoring a trial adequately representing Black patients and that company also sponsoring a trial adequately representing Latino patients, or vice versa ( values >0.05).

CONCLUSION

Diverse trial enrollment is inadequate, without improvement over time. There are bright spot trials that may merit study for factors contributing to their successful recruitment of representative patients.

摘要

目的

研究肿瘤治疗临床试验多样性随时间的变化趋势,识别充分代表黑人或拉丁裔患者的亮点试验,并研究它们与试验特征的关联。

方法

这项对支持美国食品药品监督管理局(FDA)肿瘤治疗药物批准(2012 - 2021年)的试验进行的回顾性横断面研究,将纳入试验的女性、老年人以及少数族裔患者的比例与有获批适应症的美国患者群体和美国人口普查数据进行比较,探索随时间的变化趋势。我们估计了赞助充分代表黑人患者的试验的组织同时赞助充分代表拉丁裔患者的试验的可能性,反之亦然,并研究了亮点试验(即充分代表黑人或拉丁裔患者的试验)与试验特征的关联。

结果

FDA在2012 - 2021年期间批准了来自70个申办方的111种肿瘤治疗药物,涉及121项试验,共纳入50,871名患者,其中22,155名(44%)为女性,9,442名(19%)为老年人(>64岁),5,319名(9.6%)为亚洲人,1,353名(3%)为黑人,1,511名(3%)为拉丁裔。在过去10年中,没有一项试验能充分代表所有患者人口统计学特征,且任何群体都没有改善(P值>.05),80%的试验充分代表了女性,44%的试验充分代表了老年人(>64岁),2%的试验充分代表了少数族裔患者。我们识别出33项亮点试验,其可能性与单个申办方相关(P <.0001),但与申办方规模(P =.22)、适应症(P =.20)或试验阶段(P =.32)无关。赞助充分代表黑人患者的试验的公司与赞助充分代表拉丁裔患者的试验的公司之间没有关联,反之亦然(P值>0.05)。

结论

多样化的试验入组情况不足,且未随时间改善。存在一些亮点试验,其成功招募代表性患者的因素值得研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3781/12360498/0203744b87d9/nihms-2102471-f0004.jpg

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