Division of Cancer Epidemiology & Genetics, National Cancer Institute/NIH, Bethesda, MD.
Centers for Disease Control, Atlanta, GA.
J Low Genit Tract Dis. 2020 Apr;24(2):148-156. doi: 10.1097/LGT.0000000000000526.
For the 2019 ASCCP Risk-Based Management Consensus Guidelines, we conducted a systematic review of diagnostic assays for postcolposcopy and posttreatment management.
A literature search was conducted to identify articles reporting on tests/assays for cervical cancer screening, triage, postcolposcopy surveillance, and posttreatment surveillance published between 2012 and 2019 in PubMed and Embase. Titles and abstracts were evaluated by co-authors for inclusion. Included articles underwent full-text review, data abstraction, and quality assessment. Pooled absolute pretest and posttest risk estimates were calculated for studies evaluating management of patients after treatment.
A total of 2,862 articles were identified through the search. Of 50 articles on postcolposcopy, 5 were included for data abstraction. Of 66 articles on posttreatment, 23 were included for data abstraction and were summarized in the meta-analysis. The pooled posttreatment risk of cervical intraepithelial neoplasia (CIN) 2+ in all studies was 4.8% (95% CI = 3.4%-6.8%), ranging from 0.4%-19.5% (τ = 0.57) in individual studies. Among individuals testing negative for human papillomavirus (HPV) posttreatment, the risk of CIN 2+ was 0.69% (95% CI = 0.3%-1.5%); among individuals testing positive for HPV posttreatment, the risk of CIN 2+ was 18.3% (95% CI = 12.1%-26.6%) in all studies. All risk estimates were substantially higher for liquid-based cytology. The HPV-cytology co-testing provided slightly better reassurance compared with HPV alone at the cost of much higher positivity.
Despite a large number of published studies on postcolposcopy and posttreatment surveillance, only few met criteria for abstraction and were included in the meta-analysis. More high-quality studies are needed to evaluate assays and approaches that can improve management of patients with abnormal screening.
为了制定 2019 年 ASCCP 基于风险的管理共识指南,我们对用于阴道镜检查后和治疗后管理的诊断检测方法进行了系统评价。
我们对 2012 年至 2019 年间在 PubMed 和 Embase 上发表的有关宫颈癌筛查、分流、阴道镜检查后监测和治疗后监测的检测/检测方法的文章进行了文献检索。由共同作者评估标题和摘要以确定是否纳入。纳入的文章进行了全文审查、数据提取和质量评估。对评估治疗后患者管理的研究计算了管理前后的绝对术前和术后风险估计值。
通过检索共确定了 2862 篇文章。在 50 篇关于阴道镜检查后的文章中,有 5 篇被纳入数据提取。在 66 篇关于治疗后的文章中,有 23 篇被纳入数据提取,并在荟萃分析中进行了总结。所有研究中治疗后宫颈上皮内瘤变(CIN)2+的累积风险为 4.8%(95%CI=3.4%-6.8%),范围为 0.4%-19.5%(τ=0.57)。在 HPV 检测阴性的个体中,CIN 2+的风险为 0.69%(95%CI=0.3%-1.5%);在 HPV 检测阳性的个体中,CIN 2+的风险为所有研究中 18.3%(95%CI=12.1%-26.6%)。所有风险估计值在液基细胞学中都要高得多。与单独使用 HPV 相比,HPV-细胞学联合检测在提供更好的保证的同时,阳性率也高得多。
尽管有大量关于阴道镜检查后和治疗后监测的已发表研究,但只有少数符合摘要标准并纳入荟萃分析。需要更多高质量的研究来评估可改善异常筛查患者管理的检测方法和方法。