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Increasing the efficiency of trial-patient matching: automated clinical trial eligibility Pre-screening for pediatric oncology patients

机译:提高试验患者匹配的效率:自动化的临床试验资格对儿科肿瘤患者的预筛查

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Background Manual eligibility screening (ES) for a clinical trial typically requires a labor-intensive review of patient records that utilizes many resources. Leveraging state-of-the-art natural language processing (NLP) and information extraction (IE) technologies, we sought to improve the efficiency of physician decision-making in clinical trial enrollment. In order to markedly reduce the pool of potential candidates for staff screening, we developed an automated ES algorithm to identify patients who meet core eligibility characteristics of an oncology clinical trial. Methods We collected narrative eligibility criteria from ClinicalTrials.gov for 55 clinical trials actively enrolling oncology patients in our institution between 12/01/2009 and 10/31/2011. In parallel, our ES algorithm extracted clinical and demographic information from the Electronic Health Record (EHR) data fields to represent profiles of all 215 oncology patients admitted to cancer treatment during the same period. The automated ES algorithm then matched the trial criteria with the patient profiles to identify potential trial-patient matches. Matching performance was validated on a reference set of 169 historical trial-patient enrollment decisions, and workload, precision, recall, negative predictive value (NPV) and specificity were calculated. Results Without automation, an oncologist would need to review 163 patients per trial on average to replicate the historical patient enrollment for each trial. This workload is reduced by 85% to 24 patients when using automated ES (precision/recall/NPV/specificity: 12.6%/100.0%/100.0%/89.9%). Without automation, an oncologist would need to review 42 trials per patient on average to replicate the patient-trial matches that occur in the retrospective data set. With automated ES this workload is reduced by 90% to four trials (precision/recall/NPV/specificity: 35.7%/100.0%/100.0%/95.5%). Conclusion By leveraging NLP and IE technologies, automated ES could dramatically increase the trial screening efficiency of oncologists and enable participation of small practices, which are often left out from trial enrollment. The algorithm has the potential to significantly reduce the effort to execute clinical research at a point in time when new initiatives of the cancer care community intend to greatly expand both the access to trials and the number of available trials.
机译:背景技术用于临床试验的人工资格筛选(ES)通常需要对劳动者的病历进行大量劳动审查,这需要利用许多资源。利用最先进的自然语言处理(NLP)和信息提取(IE)技术,我们力求提高临床试验注册中医师决策的效率。为了显着减少人员筛选的潜在候选人,我们开发了一种自动ES算法,以识别符合肿瘤学临床试验核心资格特征的患者。方法我们从ClinicalTrials.gov收集了叙事资格标准,以进行55项临床试验,这些试验在2009年12月1日至2011年10月31日之间积极招募了我们机构中的肿瘤患者。同时,我们的ES算法从电子健康记录(EHR)数据字段中提取了临床和人口统计信息,以代表同一时期接受癌症治疗的所有215名肿瘤患者的档案。然后,自动ES算法将试验标准与患者资料进行匹配,以识别潜在的试验患者匹配情况。在169个历史试验患者入组决策的参考集上验证了匹配表现,并计算了工作量,准确性,召回率,阴性预测值(NPV)和特异性。结果如果没有自动化,则肿瘤学家平均每个试验需要复查163名患者,以复制每个试验的历史患者入组。使用自动化ES时,该工作量减少了85%,减少到24位患者(精确度/召回率/ NPV /特异性:12.6%/ 100.0%/ 100.0%/ 89.9%)。如果没有自动化,肿瘤科医生将平均需要审查每位患者42次试验,以复制追溯数据集中发生的患者-试验匹配。借助自动ES,此工作量减少了90%,减少了四项试验(精密度/召回率/ NPV /特异性:35.7%/ 100.0%/ 100.0%/ 95.5%)。结论通过利用NLP和IE技术,自动化ES可以显着提高肿瘤科医生的试验筛查效率,并使小规模实践的参与成为可能,而小规模实践通常被排除在试验注册之外。当癌症护理界的新计划旨在大大扩展试验的可及性和可用试验的数量时,该算法具有在某个时间点显着减少执行临床研究工作的潜力。

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