Zhao Y Q, Dai Y, Dang L, Kong L H, Zhang Y, Feng R M, Qiao Y L, Lang J H
Office of Cancer Prevention and Treatment, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, China.
Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhonghua Zhong Liu Za Zhi. 2018 Oct 23;40(10):764-771. doi: 10.3760/cma.j.issn.0253-3766.2018.10.008.
To evaluate the actual efficacy of cervical cancer and precancerous lesions screening approaches in real-world regions with different economic levels in China. The demonstrative application and effect evaluation of cervical cancer screening program were conducted in 21 hospitals nationwide from 2015 to 2018. Multi-stage sampling method was adopted to divide the country into 7 large areas according to geographical location. Two to four screening sites of two types of cancer (cervical cancer and breast cancer) were selected in each area, and the grassroots screening sites were implemented under the guidance of superior hospitals. In rural areas, women were initially screened using cytology, human papillomavirus (HPV) testing and visual inspection. The women with positive cytology or visual inspection were referred for colposcopy, and the women with positive HPV infection were randomly referred for reflex cytology or visual inspection, or direct colposcopy examination. In urban areas, women were primarily randomized into cytology or HPV testing groups. The women with abnormal cytology or positive HPV 16/18 infection were directly referred for colposcopy examination, whereas the women with positive infection of the other 12 high-risk subtypes of HPV were referred for reflex cytology or colposcopy. All of recruited women would be follow-up and screened by the baseline screening techniques in the third year while the positive women underwent colposcopy examination. The positive rates, referral rates, the detection rates of grade 2 and above of cervical intraepithelial neoplasia (CIN 2+ ) were compared. A total of 63 931 women were recruited at the baseline. Among them, 11 rural sites included 33 823 women: 15 577, 11 157 and 7 089 women were screened by HPV testing, visual inspection via acetic acid or Lugol's iodine (VIA/VILI) and cytology, respectively. Additionally, 30 108 women were from 10 urban sites: 9 907 and 20 201 women were screened by cytology and HPV subtyping, respectively. The HPV positive rate for urban women was 9.34%, whereas that for rural women was 12.53%. The abnormal rate of cytology for urban women was 5.63%, and that for rural women was 4.24%. The positive rate of VIA/VILI in the rural women was 12.25% Furthermore, the detection rate of CIN2+ at the baseline was 0.56%, and that was statistically higher in HPV-positive group than cytology-positive group (<0.05). All of screening sites completed the baseline screening tasks as expected. The prevalence of HPV infection is higher in rural women than urban women. The performance of HPV testing is better than cytology for detecting CIN2+ cases. This real-world demonstration study provides evidences for cervical cancer prevention and control in different regions.
评估中国不同经济水平地区宫颈癌及癌前病变筛查方法的实际效果。2015年至2018年,在全国21家医院开展了宫颈癌筛查项目的示范应用及效果评估。采用多阶段抽样方法,根据地理位置将全国分为7个大区。每个大区选取2至4个两种癌症(宫颈癌和乳腺癌)的筛查点,基层筛查点在上级医院指导下实施。在农村地区,妇女最初采用细胞学检查、人乳头瘤病毒(HPV)检测和视诊进行筛查。细胞学检查或视诊阳性的妇女被转诊进行阴道镜检查,HPV感染阳性的妇女被随机转诊进行细胞学复查或视诊,或直接进行阴道镜检查。在城市地区,妇女主要被随机分为细胞学检查组或HPV检测组。细胞学异常或HPV 16/18感染阳性的妇女直接被转诊进行阴道镜检查,而其他12种高危HPV亚型感染阳性的妇女被转诊进行细胞学复查或阴道镜检查。所有招募的妇女在第三年将采用基线筛查技术进行随访和筛查,阳性妇女接受阴道镜检查。比较阳性率、转诊率、宫颈上皮内瘤变2级及以上(CIN 2+)的检出率。基线时共招募了63931名妇女。其中,11个农村筛查点有33823名妇女:分别有15577名、11157名和7089名妇女接受了HPV检测、醋酸或卢戈氏碘视诊(VIA/VILI)和细胞学检查。此外,30108名妇女来自10个城市筛查点:分别有9907名和20201名妇女接受了细胞学检查和HPV分型检测。城市妇女的HPV阳性率为9.34%,农村妇女为12.53%。城市妇女的细胞学异常率为5.63%,农村妇女为4.24%。农村妇女的VIA/VILI阳性率为12.25%。此外,基线时CIN2+的检出率为0.56%,HPV阳性组高于细胞学阳性组,差异有统计学意义(<0.05)。所有筛查点均如期完成了基线筛查任务。农村妇女HPV感染率高于城市妇女。HPV检测在检测CIN2+病例方面的表现优于细胞学检查。这项真实世界的示范研究为不同地区的宫颈癌防控提供了依据。