Oluloro Ann, Swisher Elizabeth M, Gray Heidi J, Goff Barbara, Doll Kemi M
Department of Obstetrics and Gynecology, University of Washington, Seattle, WA 98195, United States.
J Natl Cancer Inst. 2025 May 1;117(5):980-988. doi: 10.1093/jnci/djae338.
Racial and ethnic minorities remain underrepresented in gynecologic cancer clinical trials despite disproportionately worse oncologic outcomes. Research shows differential racial enrollment patterns because of comorbidity-based exclusion criteria. Our objective was to evaluate contemporary trends in comorbidity-based exclusion criteria among National Cancer Institute-sponsored gynecologic cancer clinical trials and protocol adherence to broadened eligibility criteria guidelines as an assessment of equitable enrollment access.
The ClinicalTrials.gov registry was queried for National Cancer Institute-sponsored gynecologic cancer clinical trials (1994-2021). Study characteristics and comorbidity-based exclusion criteria were abstracted from protocols. Descriptive statistics and temporal trends were calculated using χ2 testing with STATA v17 software.
Among 279 clinical trials identified, 65% completed enrollment, 53% were phase II, and 48% focused on ovarian cancer. Pharmaceutical agents (85%) were the primary therapeutic interventions. Several inequitably restrictive exclusion criteria increased over time such as hepatitis infection (17% in 1994-2000 vs 49% in 2015-2021, P < .001) and cardiovascular disease (47% in 1994-2000 vs 66% in 2015-2021, P = .002). A previously rare exclusion, "mental illness and/or social situations," dramatically increased from 5% to 51% (P < .001) over 3 decades. Adherence to broadened eligibility criteria recommendations was mixed. Renal function, cardiovascular disease, and performance status criteria were not broadened, but HIV, prior or concurrent malignancies, and brain metastasis criteria were.
Some, but not all, of the known restrictive comorbidity-based exclusion criteria have increased in gynecologic cancer clinical trial design, despite calls for improving racial and ethnic minority representation. Exclusion criteria are critical for trial safety, however, they must be carefully considered given the differential racial impact on eligibility.
尽管妇科癌症的肿瘤学结局在不同种族和族裔群体中差异极大,但少数族裔在妇科癌症临床试验中的代表性仍然不足。研究表明,基于合并症的排除标准导致了不同的种族入组模式。我们的目标是评估美国国立癌症研究所资助的妇科癌症临床试验中基于合并症的排除标准的当代趋势,以及方案对扩大资格标准指南的遵守情况,以此作为对公平入组机会的评估。
在ClinicalTrials.gov注册库中查询美国国立癌症研究所资助的妇科癌症临床试验(1994 - 2021年)。从方案中提取研究特征和基于合并症的排除标准。使用STATA v17软件通过χ²检验计算描述性统计数据和时间趋势。
在确定的279项临床试验中,65%完成了入组,53%为II期试验,48%聚焦于卵巢癌。药物治疗(85%)是主要的治疗干预措施。一些不公平的限制性排除标准随时间增加,如肝炎感染(1994 - 2000年为17%,2015 - 2021年为49%,P < 0.001)和心血管疾病(1994 - 2000年为47%,2015 - 2021年为66%,P = 0.002)。一种以前很少见的排除标准“精神疾病和/或社会状况”在30年里从5%急剧增加到51%(P < 0.001)。对扩大资格标准建议的遵守情况参差不齐。肾功能、心血管疾病和体能状态标准未放宽,但艾滋病毒、既往或同时存在的恶性肿瘤以及脑转移标准放宽了。
尽管呼吁提高少数族裔的代表性,但在妇科癌症临床试验设计中部分(而非全部)已知的基于合并症的限制性排除标准有所增加。排除标准对试验安全性至关重要,然而,考虑到其对资格的不同种族影响,必须谨慎权衡。