ZH

Zhonghua fu chan ke za zhi

2026-04-25

Ocena skuteczności 24 strategii wtórnej triażu w wykrywaniu zmian szyjki macicy u kobiet z dodatnim samodzielnie pobranym testem na wysokoonkogenne HPV

[Evaluating the efficiency of 24 secondary triage strategies for detecting cervical lesions of self-collected high-risk HPV-positive women].

Deng Z P, Wu D, Lai W X, Geng L N, Xiao A M, Bao J C, Qu X F, Dai W K, Du H, Wu R F

Recenzja AI

Cel badania

Celem badania była ocena skuteczności metylacji DNA, barwienia p16, genotypowania HPV oraz cytologii LBC i ich różnych kombinacji jako metod wtórnego triażu u kobiet z dodatnim wynikiem samodzielnie pobranego testu HR-HPV. Autorzy porównali te strategie z rekomendowanym sposobem postępowania według wytycznych ASCCP 2019 i chińskich zaleceń (HPV16/18 i/lub LBC ≥ ASC-US).

Metoda

Przeanalizowano dane 777 kobiet z dodatnim wynikiem HR-HPV z programu samopobrania w regionie Baise (Chiny), u których wykonano metylację DNA, p16, genotypowanie HPV i LBC, a wyniki porównano z histopatologią z biopsji celowanej w kolposkopii. Oceniano czułość, swoistość, odsetek skierowań na kolposkopię i liczbę potrzebnych kolposkopii (NNC) dla 24 strategii triażu, przyjmując jako punkt odniesienia zalecane strategie wg ASCCP i wytycznych chińskich.

Wyniki

Metylacja DNA i ekspresja p16 rosły wraz z zaawansowaniem zmian, osiągając najwyższą częstość w CIN3 i raku szyjki macicy; sama metylacja cechowała się wysoką swoistością, ale niską czułością dla CIN2+, natomiast p16 miało czułość i swoistość zbliżoną do strategii opartej na HPV16/18 i/lub LBC ≥ ASC-US, przy nieco niższym odsetku skierowań na kolposkopię. Najlepsze kombinowane strategie (np. wariant 3a) osiągały czułość podobną do wytycznych dla CIN2+ i bardzo wysoką dla CIN3+, przy porównywalnym lub mniejszym obciążeniu kolposkopią.

Znaczenie dla praktyki

Wyniki sugerują, że p16 oraz wybrane kombinacje testów (w tym metylacji) mogą w przyszłości stanowić alternatywę dla klasycznego triażu opartego na cytologii i HPV16/18, ograniczając liczbę niepotrzebnych kolposkopii bez pogorszenia wykrywalności CIN3+. Dla praktyki w Polsce, wraz z rozwojem samopobrania i szerszym dostępem do testów molekularnych, dane te wspierają rozważanie p16 jako wartościowego testu triażowego u kobiet z dodatnim HR-HPV, zwłaszcza tam, gdzie jakość lub dostępność cytologii jest ograniczona.

Abstrakt oryginalny

Objective: To evaluate the screening efficiency of gene DNA methylation testing, p16 staining, human papillomavirus (HPV) genotyping, and liquid-based cytology (LBC), and their combined strategies in self-collected high-risk HPV (HR-HPV) positive individuals. Methods: This study analyzed a subset of data from a free self-sampling cervical cancer screening program conducted in Baise, Guangxi Zhuang Autonomous Region (from May 2023 to April 2024). HR-HPV positive self-collected cases with complete data and quality control were included. Using the triage strategy recommended by the 2019 American Society for Colposcopy and Cervical Pathology (ASCCP) risk-based management guideline and the Chinese cervical cancer screening guideline [ie, HPV16/18 positivity and (or) LBC of atypical squamous cell of undetermined significance (ASCUS) or worse] as reference standard, the sensitivity, specificity, colposcopy referral rate, and the number needed to colposcopy (NNC) of various secondary triage approaches were assessed. Results: (1) A total of 777 HR-HPV positive women with complete data were analyzed. (2) Methylation positivity was significantly higher in high-risk group HPV16/18 (20.5%, 25/122) and high-intermediate-risk group HPV31/33/35/45/52/58 (17.2%, 66/381) than that in the low-risk group HPV39/51/56/59/66/68 (9.6%, 26/371; χ²=8.85 and χ²=7.59, P=0.003 and P=0.006). (3) Methylation positivity of cervical intraepithelial neoplasia (CIN)Ⅲ and cervical cancer cases (67.5%, 27/40) was significantly higher than CINⅠ cases (12.9%, 31/240), and CINⅡ cases (16.4%, 12/73), with statistically significant differences (P<0.05). The p16 positivity increased with lesion severity in all pairwise comparisons (P≤0.005 after correction). (4) When the guideline-recommended triage strategy [HPV16/18 positivity and (or) LBC≥ASCUS] was applied to this study population, using colposcopy-directed biopsy pathology as the reference standard, the sensitivity and specificity for detecting CINⅡ+ and CINⅢ+ were 69.03%, 65.21%, and 95.00%, 63.23%, respectively; the colposcopy referral rate was 39.77% (309/777), and NNC was 3.96 for CINⅡ+ and 8.13 for CINⅢ+. (5) Methylation performance: for CINⅡ+, sensitivity was 34.51% and specificity was 88.25%; for CINⅢ+, sensitivity was 67.50% and specificity was 87.79%. (6) p16 performance: the sensitivity for detecting CINⅡ+ and CINⅢ+ were 72.57% and 92.50%, respectively, which did not differ significantly from the guideline-recommended strategy (all P>0.05), whereas the specificity for CINⅡ+ and CINⅢ+ were 68.67% and 65.60%, respectively, similar to the guideline-recommended strategy (all P>0.05). The colposcopy referral rate was lower with p16 testing alone compared with the guideline-recommended strategy [37.32% (290/777) vs 39.77%; P>0.05]. (7) Combined strategy 3a achieved a sensitivity of 63.72% for detecting CINⅡ+, which was similar to the guideline-recommended strategy (P=0.109), and a sensitivity of 95.00% for detecting CINⅢ+, identical to that of the guideline-recommended strategy. The specificity of strategy 3a for CINⅡ+and CINⅢ+ were 70.18% and 68.52%, respectively, both significantly higher than those of the guideline-recommended strategy (χ²=9.75 and 12.56, all P<0.01). The colposcopy referral rate for strategy 3a was significantly lower than that of the guideline-recommended strategy [34.75% (270/777) vs 39.77%; P<0.001], with corresponding NNC of 3.75 for CINⅡ+ and 7.11 for CINⅢ+. Strategy 5a showed a sensitivity of 64.60% for detecting CINⅡ+, which was not significantly different from that of the guideline-recommended strategy (64.60% vs 69.03%; χ²=3.20, P=0.074), and a sensitivity of 95.00% for CINⅢ+, identical to that of the guideline-recommended strategy. The specificity of strategy 5a for CINⅡ+ and CINⅢ+ were 75.30% and 73.00%, respectively, both significantly higher than the guideline-recommended strategy (both P<0.001). NNC for strategy 5a was 3.25 for CINⅡ+ and 6.24 for CINⅢ+, both lower than those of the guideline-recommended strategy (3.96 and 8.13, respectively). The colposcopy referral rate for strategy 5a was also significantly lower than that of the guideline-recommended strategy [30.50% (237/777) vs 39.77%; χ²=70.01, P<0.001]. Conclusions: Among self-collected, high-risk HPV-positive individuals, combined triage strategies that integrate HPV genotyping with cytology, p16 staining and methylation testing, specifically strategy 3a and 5a, offer comparable sensitivity with superior specificity and lower referral rates versus co-testing for detecting CINⅡ+ and CINⅢ+.

Źródło

ZH

Zhonghua fu chan ke za zhi

2026-04-25

DOI: 10.3760/cma.j.cn112141-20250905-00411

PMID: 42045780

PubMed Pełny tekst

Autorzy (10)

Deng Z PWu DLai W XGeng L NXiao A MBao J CQu X FDai W KDu HWu R F
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