Principal investigator gender and clinical trial success: analysis of over 3000 obstetrics and gynecology trials

Jecca R. Steinberg MD, MSc , Julia D. Ditosto MS , Brandon E. Turner MD, MSc , Anna Marie Pacheco Young MD, MPH , Naixin Zhang MD , Danielle Strom MD , Sarah Andebrhan MD , Madeline F. Perry MD , Danika Barry MD, MPH , Kai Holder MD , Natalie A. Squires MD , Jill N. Anderson MD , Michael T. Richardson MD , Dario R. Roque MD , Lynn M. Yee MD, MPH
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引用次数: 0

Abstract

BACKGROUND

In obstetrics and gynecology (OBGYN) research, gender disparities permeate through leadership, funding, promotion, mentorship, publishing, compensation, and publicity. Few studies have investigated OBGYN clinical trial leadership as it relates to investigator gender. Thus, we undertook an investigation of principal investigator (PI) gender and clinical trial success.

OBJECTIVE

To characterize United States (US) OBGYN clinical trials by PI gender and analyze the association between PI gender and features of trial success.

STUDY DESIGN

This is a cross-sectional study of all US-based obstetric and gynecologic clinical trials registered on ClinicalTrials.gov (2007–2020). We examined associations between PI gender (ie, led by women, men, or both) and four primary outcomes that capture clinical trial success: early discontinuation (ie, absence of early discontinuation is a feature of success), reporting of complete trials to ClinicalTrials.gov, publication in a peer-reviewed journal, and clinical trial participant diversity (reporting of racial and ethnic diversity data and representation of diverse cohorts). Multivariable analyses controlled for subspecialty, multiple PI status, source of funding, primary purpose, phase, number of arms, enrollment, year of trial registration, blinding, oversight by a Data Safety Monitoring Committee, and number of study sites. Sensitivity analysis accounted for individual PI who led multiple clinical trials. Univariable and multivariable logistic regression analysis models were applied. We conducted multiple imputation for missing covariable data. There were no missing exposure or outcome data in the final cohort.

RESULTS

We reviewed 12,635 clinical trials focused on OBGYN. Of the 4342 trials with at least one site in the US, PI names were available for 3087 trials (71.1%). The majority of OBGYN trials were women-led (women 1696, 54.9%; men 1272, 41.2%, coled 119, 3.9%). A greater proportion of obstetrics trials (617, 60.0%) were women-led than gynecology trials (1079, 52.4%). Family planning had the greatest proportion of women-led trials (145, 74.7%), whereas reproductive endocrinology and infertility had the lowest (50, 30.9%). A greater proportion of industry-funded trials were led by men (123, 64.7%). In adjusted analysis, women-led trials had lower odds of early discontinuation (men-led reference; women-led adjusted odds ratio [aOR] 0.58, 95% confidence interval [CI] 0.44, 0.77). Women-led trials reported results less frequently (men-led reference; women-led aOR 0.52, CI 0.40–0.62) but no significant difference was seen in publication (men-led reference; women-led aOR 1.02, CI 0.57, 1.81). Women-led trials had greater odds of reporting race and ethnicity participant data (men-led reference; aOR 1.87, CI 1.27–2.47) but there was no difference in cohort diversity by PI gender.

CONCLUSION

Women investigators lead approximately half of OBGYN clinical trials in the US. Women-led trials discontinue less frequently, publish at similar rates, and include data on diversity more frequently than men-led trials. Women are as successful as men in conducting clinical trials and, in certain domains, more successful. Our findings place the impetus on the OBGYN professional ecosystem to support women's academic careers.
主要研究者性别与临床试验成功:超过3000个妇产科试验分析。
背景:在妇产科(OBGYN)研究中,性别差异贯穿于领导、资助、晋升、指导、出版、薪酬和宣传等各个方面。很少有研究调查妇产科临床试验领导,因为它与研究者性别有关。因此,我们进行了一项主要研究者(PI)性别和临床试验成功的调查。目的:用PI性别来描述美国OBGYN临床试验,并分析PI性别与试验成功特征的关系。研究设计:这是一项横断面研究,纳入在ClinicalTrials.gov上注册的所有美国产科和妇科临床试验(2007-2020)。我们研究了PI性别(即由女性、男性或两者领导)与临床试验成功的四个主要结局之间的关系:早期停药(即没有早期停药是成功的一个特征)、向ClinicalTrials.gov报告完整试验、在同行评审期刊上发表、临床试验参与者多样性(报告种族和民族多样性数据以及不同队列的代表)。多变量分析控制了亚专业、多个PI状态、资金来源、主要目的、阶段、武器数量、入组、试验注册年份、盲法、数据安全监测委员会的监督和研究地点的数量。敏感性分析考虑了领导多个临床试验的个体PI。采用单变量和多变量logistic回归分析模型。我们对缺失的协变量数据进行了多次插补。在最后的队列中没有缺失暴露或结果数据。结果:我们回顾了12635项针对妇产科的临床试验。在美国至少有一个站点的4342项试验中,有3087项试验(71.1%)可获得PI名称。大多数OBGYN试验是女性主导的(女性1696例,54.9%;男性1272例,41.2%,女性119例,3.9%)。女性主导的产科试验(617项,60.0%)多于妇科试验(1079项,52.4%)。女性主导的试验以计划生育为主(145项,74.7%),生殖内分泌和不孕症为主(50项,30.9%)。更大比例的工业资助试验由男性领导(123,64.7%)。在调整分析中,女性主导的试验早期停药的几率较低(男性主导的参考;女性主导的调整优势比[aOR] 0.58, 95%可信区间[CI] 0.44, 0.77)。女性主导的试验报告结果的频率较低(男性主导的参考;女性主导的aOR为0.52,CI为0.40-0.62),但在出版物中未见显著差异(男性主导的参考文献;女性主导(or 1.02, CI 0.57, 1.81)。女性主导的试验报告种族和民族参与者数据的几率更大(男性主导的参考;aOR 1.87, CI 1.27-2.47),但不同PI性别的队列多样性无差异。结论:在美国,女性研究者主导了大约一半的妇产科临床试验。与男性主导的试验相比,女性主导的试验中止的频率更低,发表的频率相似,而且包含多样性数据的频率更高。在进行临床试验方面,女性和男性一样成功,在某些领域甚至更成功。我们的研究结果推动了妇产科专业生态系统对女性学术事业的支持。
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
AJOG global reports
AJOG global reports Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Perinatology, Pediatrics and Child Health, Urology
CiteScore
1.20
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