Teixeira Julio Cesar, Vale Diama Bhadra, Campos Cirbia Silva, Bragança Joana Froes, Discacciati Michelle Garcia, Zeferino Luiz Carlos
Department of Obstetrics and Gynecology, University of Campinas (UNICAMP), Campinas, SP, Brazil.
Lancet Reg Health Am. 2021 Oct 31;5:100084. doi: 10.1016/j.lana.2021.100084. eCollection 2022 Jan.
Cervical cancer is a preventable disease, and the Brazilian screening is opportunistic and has low impact. The current study evaluated an initiative to organize screening using DNA-HPV testing as a replacement for cytology.
This demonstration study examined information from 16 384 DNA-HPV tests for screening in women aged 25-64 years from Indaiatuba city between October 2017-March 2020. The comparison was 20 284 women screened using cytology between October 2014-March 2017. The flowchart indicates the repetition of a negative test in five years. HPV16- and/or HPV18-positive tests and the 12 pooled high-risk HPV-positive tests with abnormal liquid-based cytology were referred for colposcopy. If cytology was negative, the HPV test was repeated in 12 months. The analyses evaluated coverage, age-group compliance, and cancer detected.
After 30 months, the coverage projection was greater than 80%. The age compliance for the HPV test was 99.25%, compared to 78.0% in the cytology program. The HPV test program showed 86.8% negative tests and 6.3% colposcopy referrals, with 78% colposcopies performed. The HPV testing program detected 21 women with cervical cancer with a mean age of 39.6 years, and 67% of cancers were early-stage compared to 12 cervical cancer cases detected by cytological screening (p=0.0284) with a mean age of 49.3 years (p=0.0158), and one case of early-stage (p=0.0014).
Organizing cervical cancer screening using DNA-HPV testing demonstrated high coverage and age compliance in a real-life scenario, and it had an immediate impact on cervical cancer detection at an early-stage.
University of Campinas, Indaiatuba City, and Roche Diagnostics.
宫颈癌是一种可预防的疾病,巴西的筛查是机会性的,效果不佳。本研究评估了一项以DNA-HPV检测替代细胞学检查来组织筛查的倡议。
本示范研究分析了2017年10月至2020年3月间因代亚图巴市25至64岁女性进行的16384次DNA-HPV筛查检测信息。对照组为2014年10月至2017年3月间接受细胞学筛查的20284名女性。流程图显示了五年内阴性检测的重复情况。HPV16和/或HPV18阳性检测以及12种高危型HPV合并阳性且液基细胞学异常的检测结果需转诊至阴道镜检查。如果细胞学检查为阴性,则在12个月后重复进行HPV检测。分析评估了覆盖率、年龄组依从性和癌症检出情况。
30个月后,覆盖率预测超过80%。HPV检测的年龄依从率为99.25%,而细胞学检查项目的这一比例为78.0%。HPV检测项目显示86.8%为阴性检测,6.3%转诊至阴道镜检查,其中78%进行了阴道镜检查。HPV检测项目检测出21例宫颈癌患者,平均年龄39.6岁,67%的癌症为早期;相比之下,细胞学筛查检测出12例宫颈癌患者(p=0.0284),平均年龄49.3岁(p=0.0158),其中1例为早期(p=0.0014)。
在实际情况下,使用DNA-HPV检测组织宫颈癌筛查显示出高覆盖率和年龄依从性,并对早期宫颈癌检测产生了直接影响。
坎皮纳斯大学、因代亚图巴市和罗氏诊断公司。