Gynecologic Oncology Department, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Gynecologic Oncology Department, National Institute of Cancer Research and Hospital, Dhaka, Bangladesh.
Gynecol Oncol. 2020 Sep;158(3):590-596. doi: 10.1016/j.ygyno.2020.06.496. Epub 2020 Jul 14.
The Onco E6™ Cervical Test, based on detection of the E6 oncoprotein of HPV 16 and 18 genotypes is evaluated as a screen for the early detection cervical neoplasia in resource-limited countries.
This prospective study from June 2018 to June 2019 evaluated 235 women aged 21-65 years, who came to Gynaecological Oncology Outpatient Department by VIA, cytology, E6 oncoprotein test and by colposcopy. Screen-positive women by any of the tests or women with suspicious findings were further evaluated by biopsy at colposcopy. The McNemar test was used to compare the performance of E6 oncoprotein test with other screening tests.
The E6 oncoprotein positivity rate was 6.8% (n = 16) with 81.25% HPV 16 positive and 18.75% HPV 18 positive. Among VIA positive cases (n = 100), E6 oncoprotein was positive in 9% (p < .001). In histopathology confirmed chronic cervicitis, CIN I, CIN II, CIN III and invasive cervical cancer, E6 test was positive for 2.8%, 4.7%, 25%, 50% and 100% respectively. E6 oncoprotein test had the highest specificity and Positive Predictive Value (PPV; 97% and 75%) compared to VIA (42% and 18%), cytology (95% and 46%) and colposcopy (94% and 59%). Sensitivity of the E6 oncoprotein test for detection of CIN3+ was significantly higher than that of cytology (52% VS 25%) but lower than that of VIA (52% VS 74%).
The HPV E6 oncoprotein test is highly specific and is an effective triage test to reduce colposcopy referrals for the large number of false positive test outcomes seen with VIA.
基于 HPV 16 和 18 基因型 E6 癌蛋白检测的 Onco E6™ 宫颈检测被评估为资源有限国家早期宫颈癌检测的筛查方法。
本前瞻性研究于 2018 年 6 月至 2019 年 6 月期间,共纳入 235 名年龄在 21-65 岁之间的女性,她们因阴道镜检查、细胞学检查、E6 癌蛋白检测和阴道镜下活检来到妇科肿瘤门诊就诊。通过任何一种检测方法发现的阳性筛查者,或出现可疑发现的女性,均在阴道镜下进行活检进一步评估。采用 McNemar 检验比较 E6 癌蛋白检测与其他筛查试验的性能。
E6 癌蛋白阳性率为 6.8%(n=16),其中 81.25%为 HPV 16 阳性,18.75%为 HPV 18 阳性。在阴道镜检查阳性病例(n=100)中,E6 癌蛋白阳性率为 9%(p<0.001)。在组织病理学确诊为慢性宫颈炎、CIN I、CIN II、CIN III 和浸润性宫颈癌的患者中,E6 检测分别为 2.8%、4.7%、25%、50%和 100%阳性。与阴道镜检查(42%和 18%)、细胞学检查(95%和 46%)和阴道镜检查(94%和 59%)相比,E6 癌蛋白检测具有最高的特异性和阳性预测值(97%和 75%)。E6 癌蛋白检测对 CIN3+的检出敏感性明显高于细胞学检查(52%比 25%),但低于阴道镜检查(52%比 74%)。
HPV E6 癌蛋白检测具有高度特异性,是一种有效的分流检测方法,可减少阴道镜检查的转诊,因为阴道镜检查的假阳性结果数量很大。