Tanaka Kyoko, Aoki Daisuke, Tozawa-Ono Akiko, Suzuki Nao, Takamatsu Kiyoshi, Nakamura Masaru, Tsunoda Hajime, Seino Shigeo, Kobayashi Noriko, Shirayama Takefumi, Takahashi Fumiaki
Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan,
Acta Cytol. 2020;64(5):486-491. doi: 10.1159/000507910. Epub 2020 Jun 12.
The aim of this study was to find out whether ThinPrep Integrated Imager (Hologic Inc.) screening is non-inferior to manual screening in the detection of cervical lesion.
For a total of 4,011 ThinPrep Pap test specimens stained by ThinPrep staining, manual screening (Manual arm) and ThinPrep Integrated Imager screening (Imager arm) were performed so as not to be screened by the same cytotechnologist, and the sensitivity and specificity in the detection of cervical lesion were compared using McNemar's test.
The sensitivity to detect CIN1 or more squamous cell abnormalities or glandular abnormalities was 91.67% (= 374/408, 95% confidence interval [CI]: 88.44-94.08%) for the Manual arm and 92.40% (= 377/408, 95% CI: 89.28-94.70%) for the Imager arm, and the specificity was 88.87% (= 3,113/3,503, 95% CI: 87.77-89.88%) for the Manual arm and 89.55% (= 3,137/3,503, 95% CI: 88.48-90.54%) for the Imager arm. The differences in sensitivity and in specificity, respectively, were 0.74% (95% CI: -3.14-4.61%, McNemar's test, p = 0.8041) and 0.69% (95% CI: -0.13-1.50%, McNemar's test, p = 0.1125). About the equality of sensitivity and specificity between the 2 methods, 95% CIs of the difference between sensitivity and specificity are in the clinical equivalence range of ±5%, so the Imager arm is non-inferior to the Manual arm.
The Imager arm was confirmed to have an equivalent and non-inferior capacity in the detection of cervical lesions compared with the Manual arm, suggesting that its practical application in cervical cytology tests is highly possible.
本研究旨在探讨薄层液基一体化成像系统(Hologic公司)筛查在检测宫颈病变方面是否不劣于手工筛查。
对总共4011份经薄层液基染色的巴氏试验标本,分别进行手工筛查(手工组)和薄层液基一体化成像系统筛查(成像组),且不由同一位细胞技术人员进行筛查,采用McNemar检验比较检测宫颈病变的敏感性和特异性。
手工组检测CIN1或更高级别鳞状细胞异常或腺性异常的敏感性为91.67%(=374/408,95%置信区间[CI]:88.44 - 94.08%),成像组为92.40%(=377/408,95% CI:89.28 - 94.70%);手工组的特异性为88.87%(=3113/3503,95% CI:87.77 - 89.88%),成像组为89.55%(=3137/3503,95% CI:88.48 - 90.54%)。敏感性差异为0.74%(95% CI:-3.14 - 4.61%,McNemar检验,p = 0.8041),特异性差异为0.69%(95% CI:-0.13 - 1.50%,McNemar检验,p = 0.1125)。关于两种方法敏感性和特异性的等同性,敏感性和特异性差异的95% CI在临床等效范围±5%内,因此成像组不劣于手工组。
与手工组相比,成像组在检测宫颈病变方面被证实具有等效且不劣的能力,表明其在宫颈细胞学检测中的实际应用具有很高的可能性。