首页> 外文会议>Annual International Conference of the IEEE Engineering in Medicine and Biology Society >Preliminary experimental results from multi-center clinical trials for detection of cervical precancerous lesions using the Cerviscan system: a novel full-field evoked tissue fluorescence based imaging instrument
【24h】

Preliminary experimental results from multi-center clinical trials for detection of cervical precancerous lesions using the Cerviscan system: a novel full-field evoked tissue fluorescence based imaging instrument

机译:多中心临床试验检测使用Cerviscan系统检测宫颈癌癌前病变的初步实验结果:一种新型全场诱发组织荧光成像仪

获取原文

摘要

Cervical cancer is an important cause of death in women worldwide, accounting for 190,000 deaths annually. Women are currently screened for cervical cancer using Pap smear - an imperfect technology with poor sensitivity and specificity. Furthermore, 5-10% of the Pap smear studies result in uncertain findings called ASCUS. These patients are subjected to repeat Pap smears to determine women who need further examination by colposcopy. LifeSpex, Inc. is developing the Cerviscan system - a novel, full-field multi-spectral tissue fluorescence imaging system that is designed to detect cervical precancerous lesions (i.e. SIL) in real-time. We report preliminary results from a multi-center trial for evaluating the performance of Cerviscan system. A study population of 67 subjects, in three clinical sites in the US and Canada, each underwent three procedures i.e. (a) repeat liquid-based Pap smear, (1)) Cerviscan exam, and (c) colposcopy directed biopsy exam (gold standard). Fifty-two patients for whom data from all three exams were available (i.e. 78% of the patients enrolled) are included in this preliminary analysis. A multivariate classification algorithm has been trained using data from 228 regions (82 SIL, 146 NOnSIL) in 42 women. Results are reported on an independent test set of 70 regions (25 SIL, 45 NonSIL) in 10 women. The Cerviscan system correctly identified 21/25 SIL and 42/45 NonSIL regions, giving a sensitivity of 84% and specificity of 93.3%. The Cerviscan system correctly resolved 5/7 'ASCUS+LoSIL' calls made by repeat liquid-based cytology. Furthermore, the Cerviscan system detected 2 patients with precancerous lesions that had been missed by the repeat liquid-based cytology. The Cerviscan system detects precancerous lesions with higher accuracy than repeat liquid-based Pap smear and locates lesion in real-time. The Cerviscan system has the potential of providing a tool that permits better patient management.
机译:宫颈癌是全世界妇女死亡的重要原因,每年占190,000人死亡。使用PAP涂抹的妇女筛查宫颈癌 - 一种不完美的技术,敏感性差和特异性差。此外,5-10%的PAP涂片研究导致了名为ASCUS的不确定发现。这些患者进行重复蛋白涂片以确定需要通过阴道镜检查进一步检查的妇女。 LifeSpex,Inc。正在开发Cerviscan系统 - 一种新颖的全场多光谱组织荧光成像系统,用于实时检测宫颈癌癌前病变(即SIL)。我们向评估Cerviscan系统的性能进行评估的多中心试验报告初步结果。在美国和加拿大的三个临床部位,每次研究人口67名受试者,每次三个程序,即(a)重复基于液体的PAP涂片,(1))Cerviscan考试,和(c)Colposcopy定向活组织检查检查(金标准)。五十二名患者可获得来自所有三项考试的数据(即78%的注册患者)包含在此初步分析中。已经使用来自228个地区(82 SIL,146 Nonsil)的数据训练了多变量分类算法。结果报告了10名妇女的独立测试组(25 Sil,45个非Nonsil)。 Cerviscan系统正确鉴定了21/25 Sil和42/45个非尼尔区,敏感性为84%,特异性为93.3%。 Cerviscan系统通过重复基于液体的细胞学进行了正确解决了5/7'Ascus + Losil'呼叫。此外,宫颈癌系统检测到2例患有由重复液体的细胞学错过的癌前病变的患者。 Cerviscan系统检测癌前病变,比重复液体的PAP涂抹更高的精度,并实时定位病变。 Cerviscan系统具有提供允许更好的患者管理的工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号