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Table 3 Results of cytology and HR-HPV co-testing performed within 6 months before histological diagnosis of invasive cervical adenocarcinoma

From: Prior cervical cytology and high-risk HPV testing results for 311 patients with invasive cervical adenocarcinoma: a multicenter retrospective study from China’s largest independent operator of pathology laboratories

Cytology

HC2 testing (n = 24)

Genotyping (n = 45)

Total (n = 69)

Negative (%)

Positive (%)

Negative (%)

Positive (%)

Negative (%)

Positive (%)

NILM

3 (12.5)

6 (25.0)

6 (13.3)

1 (2.2)

9 (13.0)

7 (10.1)

Unsatisfactory

0 (0)

1 (4.2)

0 (0)

1 (2.2)

0 (0)

2 (2.9)

ASC-US

1 (4.2)

4 (16.7)

3 (6.7)

1 (2.2)

4 (5.8)

5 (7.2)

ASC-H

0 (0)

2 (8.3)

1 (2.2)

5 (11.1)

1 (1.4)

7 (10.1)

HSIL

0 (0)

0 (0)

0 (0)

2 (4.4)

0 (0)

2 (2.9)

Cancer cells

0 (0)

2 (8.3)

2 (4.4)

8 (17.8)

2 (2.9)

10 (14.5)

AGC

2 (8.3)

3 (12.5)

5 (11.1)

10 (22.2)

7 (10.1)

13 (18.8)

Total

6 (25.0)

18 (75.0)

17 (37.8)

28 (62.2)

23 (33.3)

46 (66.7)

  1. HR-HPV, High-risk human papillomavirus; HC2, Hybrid Capture 2; NILM, negative for intraepithelial lesion or malignancy; ASC-US, Atypical squamous cells of undetermined significance; ASC-H, Atypical squamous cells—cannot exclude HSIL; HSIL, High-grade squamous intraepithelial lesion; AGC, Atypical glandular cells