University of Virginia Health, Charlottesville, VA 22908, USA.
Becton, Dickinson and Company, BD Life Sciences - Integrated Diagnostic Solutions, 7 Loveton Circle, Sparks, MD 21152, USA.
Gynecol Oncol. 2023 Jul;174:68-75. doi: 10.1016/j.ygyno.2023.04.022. Epub 2023 May 5.
Optimizing the balance between colposcopy referrals and the detection of high-grade cervical intraepithelial neoplasia (CIN) during cervical cancer screening requires robust triage strategies. We evaluated the performance of extended HPV genotyping (xGT), in combination with cytology triage, and compared it to previously published performance data for high-grade CIN detection by HPV16/18 primary screening in combination with p16/Ki-67 dual staining (DS).
The baseline phase of the Onclarity trial enrolled 33,858 individuals, yielding 2978 HPV-positive participants. Risk values for ≥CIN3 were determined for Onclarity result groupings corresponding to HPV16, not HPV16 but HPV18 or 31, not HPV16/18/31 but HPV33/58 or 52, not HPV16/18/31/33/58/52 but HPV35/39/68 or 45 or 51 or 56/59/66 across all cytology categories. Published data from the IMPACT trial for HPV16/18 plus DS was utilized as a comparator during ROC analyses.
There were 163 ≥ CIN3 cases detected. The ≥CIN3 risk stratum hierarchy (% risk of ≥CIN3) that resulted from this analysis included: >LSIL (39.4%); HPV16, ≤LSIL (13.3%); HPV18/31, ≤LSIL (5.9%); HPV33/58/52/45, ASC-US/LSIL (2.4%); HPV33/58/52, NILM (2.1%); HPV35/39/68/51/56/59/66, ASC-US/LSIL (0.9%); and HPV45/35/39/68/51/56/59/66, NILM (0.6%). For ≥CIN3 ROC analysis, the optimal cutoff for sensitivity versus specificity was approximated between not HPV16 but HPV18 or 31, any cytology (≥CIN3 sensitivity = 85.9% and colposcopy-to- ≥ CIN3 = 7.4) and not HPV16/18/31 but HPV33/58/52, NILM (≥CIN3 sensitivity = 94.5% and colposcopy-to- ≥CIN3 = 10.8). HPV16/18 with DS triage showed a sensitivity of 94.3%, with a colposcopy-to- ≥ CIN3 ratio of 11.4.
xGT performed similarly compared to HPV primary screening plus DS for detection of high-grade CIN. xGT provides results that stratify risk in a flexible and reliable manner for colposcopy risk thresholds set by different guidelines or organizations.
在宫颈癌筛查中,优化阴道镜转诊和高级别宫颈上皮内瘤变(CIN)检出之间的平衡需要强有力的分流策略。我们评估了扩展型 HPV 基因分型(xGT)与细胞学分流相结合的性能,并将其与之前发表的 HPV16/18 初筛联合 p16/Ki-67 双重染色(DS)检测高级别 CIN 的性能数据进行了比较。
Onclarity 试验的基线阶段招募了 33858 人,产生了 2978 名 HPV 阳性参与者。对于 Onclarity 结果分组对应的≥CIN3 风险值,确定了 HPV16、非 HPV16 但 HPV18 或 31、非 HPV16/18/31 但 HPV33/58 或 52、非 HPV16/18/31/33/58/52 但 HPV35/39/68 或 45 或 51 或 56/59/66 在所有细胞学类别中。利用 IMPACT 试验中 HPV16/18 加 DS 的发表数据在 ROC 分析中作为对照。
共检出 163 例≥CIN3 病例。由此分析得出的≥CIN3 风险分层(≥CIN3 的风险百分比)包括:>LSIL(39.4%);HPV16,≤LSIL(13.3%);HPV18/31,≤LSIL(5.9%);HPV33/58/52/45,ASC-US/LSIL(2.4%);HPV33/58/52,NILM(2.1%);HPV35/39/68/51/56/59/66,ASC-US/LSIL(0.9%);HPV45/35/39/68/51/56/59/66,NILM(0.6%)。对于≥CIN3 的 ROC 分析,敏感性与特异性的最佳截断值在非 HPV16 但 HPV18 或 31 与任何细胞学(≥CIN3 敏感性=85.9%和阴道镜至≥CIN3=7.4)和非 HPV16/18/31 但 HPV33/58/52,NILM(≥CIN3 敏感性=94.5%和阴道镜至≥CIN3=10.8)之间接近。HPV16/18 加 DS 分流检测的敏感性为 94.3%,阴道镜至≥CIN3 的比值为 11.4。
xGT 与 HPV 初筛加 DS 相比,在检测高级别 CIN 方面表现相似。xGT 提供的结果以灵活可靠的方式对不同指南或组织设定的阴道镜风险阈值进行分层风险。