Alexander Marliese, Solomon Benjamin, Ball David L, Sheerin Mimi, Dankwa-Mullan Irene, Preininger Anita M, Jackson Gretchen Purcell, Herath Dishan M
Department of Pharmacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.
JAMIA Open. 2020 May 1;3(2):209-215. doi: 10.1093/jamiaopen/ooaa002. eCollection 2020 Jul.
The objective of this technical study was to evaluate the performance of an artificial intelligence (AI)-based system for clinical trials matching for a cohort of lung cancer patients in an Australian cancer hospital.
A lung cancer cohort was derived from clinical data from patients attending an Australian cancer hospital. Ten phases I-III clinical trials registered on clinicaltrials.gov and open to lung cancer patients at this institution were utilized for assessments. The trial matching system performance was compared to a gold standard established by clinician consensus for trial eligibility.
The study included 102 lung cancer patients. The trial matching system evaluated 7252 patient attributes (per patient median 74, range 53-100) against 11 467 individual trial eligibility criteria (per trial median 597, range 243-4132). Median time for the system to run a query and return results was 15.5 s (range 7.2-37.8). In establishing the gold standard, clinician interrater agreement was high (Cohen's kappa 0.70-1.00). On a per-patient basis, the performance of the trial matching system for eligibility was as follows: accuracy, 91.6%; recall (sensitivity), 83.3%; precision (positive predictive value), 76.5%; negative predictive value, 95.7%; and specificity, 93.8%.
The AI-based clinical trial matching system allows efficient and reliable screening of cancer patients for clinical trials with 95.7% accuracy for exclusion and 91.6% accuracy for overall eligibility assessment; however, clinician input and oversight are still required. The automated system demonstrates promise as a clinical decision support tool to prescreen a large patient cohort to identify subjects suitable for further assessment.
本技术研究的目的是评估澳大利亚一家癌症医院中基于人工智能(AI)的系统对一组肺癌患者进行临床试验匹配的性能。
从澳大利亚一家癌症医院患者的临床数据中提取肺癌队列。利用在clinicaltrials.gov上注册并对该机构的肺癌患者开放的10项I - III期临床试验进行评估。将试验匹配系统的性能与由临床医生共识确定的试验资格金标准进行比较。
该研究纳入了102名肺癌患者。试验匹配系统针对11467条个体试验资格标准(每项试验中位数为597条,范围为243 - 4132条)评估了7252个患者属性(每位患者中位数为74个,范围为53 - 100个)。系统运行查询并返回结果的中位时间为15.5秒(范围为7.2 - 37.8秒)。在建立金标准时,临床医生之间的评分者间一致性较高(科恩kappa系数为0.70 - 1.00)。基于每位患者,试验匹配系统在资格评估方面的性能如下:准确率为91.6%;召回率(敏感性)为83.3%;精确率(阳性预测值)为76.5%;阴性预测值为95.7%;特异性为93.8%。
基于人工智能的临床试验匹配系统能够高效且可靠地筛选癌症患者参与临床试验,排除的准确率为95.7%,总体资格评估的准确率为91.6%;然而,仍需要临床医生的参与和监督。该自动化系统有望作为一种临床决策支持工具,对大量患者队列进行预筛选,以识别适合进一步评估的受试者。