Screening History in Vaginal Precancer and Cancer: A Retrospective Study of 2131 Cases in China.

PURPOSE: To examine the screening history of vaginal intraepithelial neoplasia (VaIN) and vaginal cancer. PATIENTS AND METHODS: We included women with histologically confirmed VaIN or vaginal cancer by colposcopy-directed biopsy between 1 January 2019 and 31 December 2019. The results of cytology, hrHPV, colposcopic examination and history of hysterectomy were retrospectively analysed.
RESULTS: A total of 26,432 colposcopies were performed during the study period, among which 2131 women (1835 [86.1%] with VaIN 1; 268 [12.6%] with VaIN 2/3; and 28 [1.3%] with vaginal cancer) were retrospectively studied. hrHPV test positivity was significantly higher than that of cytology for VaIN 1 (84.4% vs 67.3%; P < 0.001) and VaIN 2/3 (92.0% vs 79.9%; P < 0.001) but not for vaginal cancer (84.6% vs 78.6%; P = 0.73). Additionally, the concordance rates for colposcopic impression were 79.5%, 54.5%, and 92.8% for VaIN1, VaIN2/3, and vaginal cancer, respectively. All 372 patients had a history of hysterectomy, and 81.0% (282/348) of indications were related to cervical precancer and cancer. Although cytology test positivity was significantly higher in patients with hysterectomy than in patients without hysterectomy (76.2% vs 67.5%; P < 0.001), cytology combined with hrHPV can help to detect more than 95% of VaIN and vaginal cancer cases in both groups (96.2% for patients with hysterectomy and 96.5% for patients without hysterectomy).
CONCLUSION: VaIN and vaginal cancer are not rare diseases. Although cytology was sensitive (67.5%-76.2%) for detecting vaginal lesions regardless of hysterectomy, cytology combined with hrHPV improves detection accuracy up to 95% in both groups.

Introduction

Vaginal intraepithelial neoplasia (VaIN) and vaginal cancer are caused by human papilloma virus (HPV) infection of the vagina.1–4 VaIN 2/3 is a precancerous lesion that is analogous to cervical intraepithelial neoplasia (CIN) 2/3, whereas VaIN 1 is the benign vaginal manifestation of HPV infection.5,6 Other known risk factors for VaIN and vaginal cancer include immunosuppression, smoking, multiple intercourse partners, and early coitarche.7,8 Additionally, a history of cervical lesions and previous hysterectomy for HPV-related cervical diseases are other major risk factors.9,10

The incidence of VaIN has been increasing steadily because of widespread cytology with high-risk HPV (hrHPV) cotesting and colposcopy. At the largest obstetrics and gynecology tertiary teaching hospital in China, the mean detection rate of VaIN in all lower genital tract intraepithelial lesions was reportedly 11.49% (1923/16,732), which increased from 8.09% in 2013 to 13.08% in 2015.11 However, most vaginal lesions are diagnosed during cervical cancer screening, and there are no guidelines for specifically conducting screening for vaginal lesions. In addition, cytology and hrHPV tests were performed above the surface of the cervix. Little is known about whether cervical screening is the appropriate clinical choice for the detection of vaginal lesions.3,12–16 Because of the reasons above, we aimed to explore the roles of cervical screening history, including cytology, hrHPV genotyping, and colposcopic examinations, in colposcopy-directed biopsy (CDB)-confirmed VaIN and vaginal cancer (VaIN+).

Patients and Methods

Study Population

As the largest OBGYN referral centre in China, we admit VaIN and vaginal cancer patients across the country. The inclusion criterion included women visiting our hospital in Yangpu District between 1 January 2019 and 31 December 2019. VaIN or vaginal cancers were histologically diagnosed under CDB and either performed in our hospital or by a referring institution. Any cervical cancer case with vaginal invasion was excluded. For repeat patients, we chose the first time they underwent CDB during this period.

Permission was granted by the institutional review board of the Obstetrics and Gynecology Hospital of Fudan University before data extraction was performed. All available data, including age, history of surgery, cytology results, hrHPV test results, colposcopic examination results, and pathology results, were extracted from medical records. For patients referred to our hospital, original pathologic specimens were re-examined by a senior pathologist, and colposcopy was performed by a senior colposcopist to revalidate the presence or absence of invasive lesions, with subsequent biopsies performed for areas suspected of neoplasia.

Cytology Screening Testing

A liquid-based Pap test (SurePathTM; Becton, Dickinson, Franklin Lakes, NJ, USA) was used for cytology testing. The results, including negative for intraepithelial lesion or malignancy (NILM), atypical squamous cells of undetermined significance (ASC-US), low-grade squamous intraepithelial lesion (LSIL), atypical squamous cells that cannot exclude HSIL (ASC-H), high-grade squamous intraepithelial lesion (HSIL), atypical glandular cells (AGC), and squamous cell carcinoma (SCC), were reported using the Bethesda System.

hrHPV DNA Screening

hrHPV testing was performed using hybrid capture-2 testing (Digene, Maryland, USA), the Cobas 4800 assay (Roche, Penzberg, Germany) or a fluorescence-based multiplex real-time HPV DNA genotyping kit (Bioperfectus, Jiangsu, China), which can detect high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68.

Colposcopic Examination

Cytology/hrHPV testing was performed at the clinic within 6 weeks before colposcopy. Oestrogen was applied prior to colposcopic examinations among postmenopausal women. The indications for colposcopy at our hospital were as follows: abnormal cytology results (ASCUS, LSIL, HSIL, ASC-H, AGC, SCC); positive hrHPV results; symptoms or signs of possible cervical/vaginal/vulvar cancer, including any suspicious cervical abnormality found during pelvic examination, abnormal genital tract bleeding, or unexplained cervicovaginal discharge; first follow-up after cervical conization; and first follow-up after hysterectomy indicated for cervical cancer or HSIL. Colposcopic examinations and diagnoses were performed by experienced colposcopists following the 2011 International Federation of Cervical Pathology and Colposcopy terminology.17 A detailed description of colposcopic findings and initial diagnosis were recorded based on our previous study:18 1) General assessment: adequate or inadequate; 2) Normal colposcopic findings: mature or atrophic squamous epithelium; 3) Abnormal colposcopic findings: the location (anterior, posterior, or lateral) and total size of the lesion; the maximum size of single lesion and the number of lesions; Grade 1 (minor) including thin acetowhite epithelium, fine punctuation and fine mosaic; Grade 2 (major) including dense acetowhite epithelium, coarse punctuation and coarse mosaic; suspicious for invasion including atypical vessels, fragile vessels, and an irregular surface; and nonspecific findings including columnar epithelium (adenosis); 4) Miscellaneous findings: erosion, condyloma, polyp, cyst, endometriosis, etc; 5) Finally, colposcopic impression was reckoned, which was classified as normal or benign lesion, VaIN 1, VaIN 2/3, or suspicion of cancer. Based on the application of 5% acetic solution and Lugol’s iodine solution, targeted biopsies of suspected cervical, vaginal, and vulvar lesions were performed. For patients after hysterectomy, we specifically inspected the 2 ends of the vault suture line to avoid hidden vaginal lesions in vaginal dimples.

Statistical Analysis

Data calculation was performed using SPSS version 24.0 (IBM, Armonk, NY, USA). Normally distributed continuous variables are expressed as the mean ± SD, and nonnormally distributed continuous variables are expressed as the median (interquartile range, IQR). Categorical variables are presented as numbers and proportions. The Kruskal–Wallis test was used to compare continuous variables, whereas the chi-square or Fisher’s exact tests were used for categorical variables. A two-tailed P-value <0.05 was deemed statistically significant.

The parameters listed below were calculated for the HPV16, HPV18 and non16/18HPV groups.

hrHPV test positivity (hrHPV positive tests/HPV tests).

Cytology test positivity (abnormal cytology tests/cytology tests).

Cytology and hrHPV cotesting positivity (women with hrHPV-positive tests or abnormal cytology tests/women who underwent cytology and hrHPV cotesting).

Concordance rate of the colposcopic impression (women with colposcopic impression met CDB pathology/women with colposcopic impression).

Results

The numbers of cytology and hrHPV screenings performed in 2019 were 109,009 and 76,189, respectively. In Yangpu district, a total of 26,432 colposcopies were performed. Based on the histologic results, 8.1% were VaIN+. As the largest OBGYN referral centre in China, most patients were referred to our hospital with abnormal cervical screening results; therefore, the exact prevalence of vaginal lesions cannot be calculated.

A total of 2,131 women were included, as follows: 1835 (86.1%) with VaIN 1; 268 (12.6%) with VaIN 2/3; and 28 (1.3%) with vaginal cancer. The clinical characteristics of women with VaIN and vaginal cancer are presented in Table 1. The median age was 48 years (IQR, 35–56 years). Women with VaIN 1 were younger than women with VaIN 2/3 and vaginal cancer (47 years vs 52 and 53.5 years; P < 0.001). Approximately 1260 (59.1%) patients were diagnosed with only vaginal lesions. Among 871 patients with concomitant lesions, 81.3% had cervical lesions, 10.3% had vulvar lesions, and 8.4% had both. The rates of concomitant lesions with VaIN 1 and VaIN 2/3 were similar (41.3% vs 39.6%); however, the rate was lowest with vaginal cancer (25.0%; P = 0.19).

Table 1

Clinical Characteristics of 2131 Women with VaIN and Vaginal Cancer

Characteristics	VaIN 1	VaIN 2/3	Vaginal Cancer	P-value
Age(y), Median (IQR)	47 (34–56)	52 (42–61)	53.5 (40–62.5)	<0.01
Cytology, n (%)
NLIM	599 (32.7)	53 (20.1)	6 (21.4)
ASCUS or LSIL	1147 (62.7)	132 (50.0)	8 (28.6)
AGC, ASC-H or HSIL+	85 (4.6)	79 (29.9)	14 (50.0)
hrHPV infection, n (%)				<0.01
No	285 (15.6)	21 (8.0)	4 (15.4)
Yes	1545 (84.4)	243 (92.0)	22 (84.6)
Cotesting sensitivity, n (%)				0.02
No	74 (4.1)	1 (0.4)	1 (3.8)
Yes	1752 (95.9)	261 (99.6)	25 (96.2)
Colposcopy impression, n (%)				<0.01
Normal	225 (12.3)	8 (3.0)	0 (0.0)
VaIN 1	1459 (79.5)	103 (38.4)	1 (3.6)
VaIN 2/3	151 (8.2)	146 (54.5)	1 (3.6)
Vaginal cancer	0 (0.0)	11 (4.1)	26 (92.8)
Concomitant lesion, n (%)				0.19
No	1077 (58.7)	162 (60.4)	21 (75.0)
Yes	758 (41.3)	106 (39.6)	7 (25.0)
Hysterectomy, n (%)				<0.01
No	1590 (86.6)	158 (59.0)	11 (39.3)
Yes	245 (13.4)	110 (41.0)	17 (60.7)

Note: hrHPV including HPV 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68.

Abbreviations: VaIN, vaginal intraepithelial neoplasia; NLIM, negative for intraepithelial lesion or malignancy; ASCUS, atypical squamous cells of undetermined significance; ASC-H, atypical squamous cells, cannot exclude high-grade squamous intraepithelial lesion; LSIL, low-grade squamous intraepithelial lesion; HSIL, high-grade squamous intraepithelial lesion; AGC, atypical glandular cells; IQR, interquartile range.

Twenty-eight patients had vaginal cancer. Only half of them had HSIL+ cytology results, whereas 84.6% (22/26) had positive hrHPV results and 75.0% (15/20) had HPV 16 infection among positive hrHPV genotyping tests. Approximately 92.8% of vaginal cancer diagnoses were consistent with the colposcopic impressions. Seventeen patients had a history of hysterectomy because of cervical lesions (n = 16) or endometrial cancer (n = 1).

Cytology and hrHPV Screening

The overall positivity was highest in cytology and hrHPV cotesting, followed by hrHPV testing alone and cytology alone (96.5%, 85.4% and 69.0%; P < 0.001).

A total of 2123 cytology results were available. The detailed cytology reports are presented in Table 2. The cytology test positivity for vaginal cancer and VaIN 2/3 was higher than that for VaIN 1 (78.6% and 79.9% vs 67.3%; P < 0.001). Based on the cytology tests, cytology test positivity was highest in patients who had undergone hysterectomy and lowest in patients without cervical lesions in their intact uterus (76.2% and 61.5%; P < 0.001). Concomitant cervical lesions also increased the cytology test positivity to 75.0% (Figure 1).

Table 2

Detailed Cytology Results of 2123 Women with VaIN and Vaginal Cancer

Cytology Test Results	NLIM	ASCUS	LSIL	HSIL	ASC-H	SCC	AGC	Total	Positivity
VaIN 1	599	425	722	59	23	1	2	1831	67.3%
VaIN 1 with uterus	534	361	624	45	19	1	2	1586	66.3%
Without cervical lesion	355	214	315	12	10	0	1	907	60.9%
Concomitant cervical lesion	179	147	309	33	9	1	1	679	73.6%
VaIN 1 after hysterectomy	65	64	98	14	4	0	0	245	73.5%
VaIN 2/3	53	53	79	60	14	4	1	264	79.9%
VaIN 2/3 with uterus	35	31	46	34	7	3	0	156	77.6%
Without cervical lesion	20	13	22	7	1	2	0	65	69.2%
Concomitant cervical lesion	15	18	24	27	6	1	0	91	83.5%
VaIN 2/3 after hysterectomy	18	22	33	26	7	1	1	108	83.3%
Vaginal cancer	6	6	2	10	1	3	0	28	78.6%
Vaginal cancer with uterus	1	4	1	4	0	1	0	11	90.9%
Without cervical lesion	1	2	0	1	0	0	0	4	75.0%
Concomitant cervical lesion	0	2	1	3	0	1	0	7	100.0%
Vaginal cancer after hysterectomy	5	2	1	6	1	2	0	17	70.6%
Total	658	803	129	484	38	8	3	2123	69.0%

Notes: Positivity, abnormal cytology tests /cytology tests.

Abbreviations: VaIN, vaginal intraepithelial neoplasia; NLIM, negative for intraepithelial lesion or malignancy; ASCUS, atypical squamous cells of undetermined significance; ASC-H, atypical squamous cells, cannot exclude high-grade squamous intraepithelial lesion; LSIL, low-grade squamous intraepithelial lesion; HSIL, high-grade squamous intraepithelial lesion; AGC, atypical glandular cells. SCC, squamous cell carcinoma.

Figure 1

The positivity of cytology, hrHPV and cotesting in VaIN and vaginal cancer.

A total of 2120 hrHPV results were available for 2131 women with VaIN or vaginal cancer. Of these, 143 underwent hybrid capture-2 testing, 581 underwent Cobas testing, and 1396 underwent BMRT genotyping. The hrHPV test positivity was highest for VaIN 2/3 at 92.0%, which was significantly higher than those for VaIN 1 (84.4%) and vaginal cancer (84.6%). hrHPV test positivity was slightly higher among patients after hysterectomy than among patients without cervical lesions, but no significant difference was found (85.0% vs 82.5%; P = 0.289).

Among hrHPV-positive patients using BMRT genotyping, HPV 16 was the most prevalent HPV type, with a positivity of 26.5%, followed by HPV 52 (24.3%), HPV 58 (22.5%) and HPV 56 (12.6%). The detailed ranking of infected hrHPV genotypes among VaIN 1, VaIN 2/3, and vaginal cancer is illustrated in Figure 2. More than half of the patients with VaIN 2/3 (64.5%) and vaginal cancer (88.9%) were infected with HPV 16, while HPV 52 (25.9%) and HPV 58 (24.1%) were more prevalent than HPV 16 (20.4%) in patients with VaIN 1.

Figure 2

Distribution of hrHPV in VaIN and vaginal cancer.

Regardless of the degree of vaginal lesions and the hysterectomy history, the cytology and hrHPV cotesting positivity was above 95%. There was no significant difference in cotesting positivity between patients after hysterectomy and patients without cervical lesions.

Seventy-six patients had negative cotesting test. The indications for colposcopy were as follows: abnormal genital tract bleeding or unexplained cervicovaginal discharge; first follow-up after cervical conization; and first follow-up after hysterectomy indicated for cervical cancer or HSIL. Among them, one patient was confirmed to have VaIN 2/3 and another patient was confirmed to have vaginal cancer. Both underwent hysterectomy for cervical HSIL.

Colposcopic Impression

All of the colposcopy records were available. The concordance rates of the colposcopic impression were 79.5% (1459/1835), 54.5% (146/243), and 92.8% (26/28) for patients with VaIN 1, VaIN 2/3, and vaginal cancer, respectively. Approximately 41.4% of VaIN 2/3 patients were underestimated by colposcopic impression.

Hysterectomy History

All 372 women with a history of hysterectomy underwent either total or radical hysterectomy. Among them, 348 hysterectomy indications were available (Table 3). Overall, the most common indications were precancerous cervical lesions (44.8%) and overt cancer (36.2%). For patients with vaginal cancer, 94.5% (16/17) of the patients underwent hysterectomy for cervical lesions, while the other hysterectomy indication was endometrial cancer. Two patients (aged 38 and 46 years) underwent hysterectomy and partial vaginectomy because of vaginal cancer. Both of them had VaIN 1 diagnosed several years after surgery.

Table 3

Indications and Rates of Previous Hysterectomy in 348 VaIN and Vaginal Cancer Patients

Indications of Hysterectomy	VaIN 1		VaIN 2/3		Vaginal Cancer		Total
	n	%	n	%	n	%	n	%
Cervical lesions
Cervical cancer	81	35.5	33	32.0	12	70.6	126	36.2
Cervical precancer lesion	95	41.7	57	55.3	4	23.5	156	44.8
Noncervical lesions
Vaginal cancer*	2	0.9	0	0.0	0	0.0	2	0.6
Endometrial cancer	6	2.6	1	1.0	1	5.9	8	2.3
Ovarian cancer	0	0.0	1	1.0	0	0.0	1	0.3
Benign disease^	44	19.3	11	10.7	0	0.0	55	15.8
Total	228	100.0	103	100.0	17	100.0	348	100.0

Notes: *One patient had hysterectomy and follow-up radiotherapy for vaginal primary mucinous adenocarcinoma 5 years ago. The other patient was diagnosed with vaginal squamous cell carcinoma and underwent surgery 3 years ago. ^Benign diseases including myoma, adenomyosis, uterine prolapse, endometrial hyperplasia, obstetrics reasons.

Abbreviation: VaIN, vaginal intraepithelial neoplasia.

The proportions of VaIN 2/3 and vaginal cancer were significantly higher in patients who had undergone hysterectomy. The median age of patients who had undergone hysterectomy was 10 years older than that of patients who had not (P < 0.001). The sensitivity of cytology was higher in patients who had undergone hysterectomy (P = 0.001), whereas the sensitivity values of hrHPV and concurrent cytology/hrHPV testing were not significantly different (P = 0.87 and P = 0.88, respectively).

Discussion

Compared with CIN, VaIN+ has not been sufficiently researched. The incidence of VaIN (0.2–0.3 per 100,000 women) in most studies was reported by epidemiological research involving large samples published in 1977, which was almost 50 years ago.19 However, since then, developments in medical instruments and medical care have improved. We previously reported 16,732 women diagnosed with CIN (83.99%; 14,053/16,732), VaIN (11.49%; 1923/16,732), and VIN (4.52%; 756/16,732) at our hospital between 2013 and 2015.11 The annual number of VaIN+ cases in 2019 was 2131, which is approximately sixfold that of 2013. Hence, VaIN+ is not a rare disease during colposcopy. One reason for the rapidly increased number of diagnosed cases could be that the total number of CDB increased annually at our hospital. Furthermore, increasing attention has been focused on VaIN+ by colposcopists. Therefore, the current actual prevalence of VaIN+ might be much higher than what has been reported.

With a rapid increase in the prevalence of VaIN+, there are no guidelines for vaginal lesion screening. Most VaIN+ was found at the time of cervical screening. However, since we perform cytology screening on the cervical surface, there is doubt whether it is enough for the detection of VaIN+. Few studies have explored the value of cytology for VaIN or vaginal cancer.20–22 A meta-analysis by Khan et al indicated that for patients with VaIN 2/3 who have undergone hysterectomy, the cytology test positivity was 83% and the positive predictive value ranged from 0% to 14%.23 Our study showed that cytology test positivity was 79.9% for VaIN 2/3 and 78.6% for vaginal cancer; however, it was only 67.6% for VaIN 1. Despite differences in cytology results, the positivity of cotesting with and without hysterectomy was more than 95%.

Studies have demonstrated that various HPV types might have different roles in the risk of CIN and cervical cancer progression.24 However, few studies have focused on the role of HPV infection in VaIN+. Only 3 studies involving more than 100 cases analyzed the HPV genotyping distribution in VaIN+.12,14,15 Alemany et al performed a worldwide cross-sectional study of 189 VaIN 2/3 cases and 408 vaginal cancer cases in 31 countries from 1986 to 2011 and reported that the HPV prevalence was 96% with VaIN 2/3 lesions and 74% with vaginal cancer.15 Bertoli et al reported that the pooled HPV prevalence was 85.2% with VaIN and 66.7% with vaginal cancer.25 Furthermore, the most predominant HPV type was found to be HPV 16, followed by HPV 33 in VaIN and HPV 18 in vaginal cancer. Our study included 2131 Chinese women with VaIN+; hrHPV test positivity was 84.4% for patients with VaIN 1, 92.0% for patients with VaIN 2/3, and 84.6% for patients with vaginal cancer. Similarly, HPV 16 was the predominant genotype; it was found in 64.5% of VaIN 2/3 cases and 88.9% of vaginal cancer cases among hrHPV-positive patients. HPV 52, HPV 58, and HPV 18 were more prevalent than HPV 33 in patients with VaIN2/3, and HPV 58 and HPV 66 were more prevalent than HPV 18 in patients with vaginal cancer. In contrast, HPV 52 (25.9%) was the predominant type found in patients with VaIN 1, followed by HPV 58 (24.1%) and HPV 16 (20.4%).

CDB is critical for detecting precancer and cancer of the cervix and vagina. Accumulating studies have indicated the poor accuracy and specificity of colposcopic impressions when diagnosing cervical neoplasia.26,27 Because of its rarity, the accuracy of colposcopic examinations for detecting VaIN+ remains unclear. Only one study of VaIN revealed that the colposcopy impression accuracy was 52.2%, with higher accuracy observed for VaIN 2/3 patients (82.5%) than for VaIN 1 patients (45.0%). Furthermore, the detection rate of VaIN 2/3 may be improved if testing is performed by a highly experienced practitioner.13 Our previous study of vaginal cancer demonstrated that colposcopic examination is not only pivotal for the evaluation of abnormal cytology/hrHPV tests after hysterectomy but also decision-making for vaginectomy in the detection of early cancer.28 In the present study, the overall agreement of colposcopy and biopsy results was 76.5%; the agreement of colposcopy and biopsy results for VaIN 1, VaIN 2/3 and vaginal cancer was 79.5%, 54.5% and 92.8%, respectively (P < 0.001).

Various studies have shown that a history of CIN 2/3 and cervical cancer was strongly associated with VaIN+. Cervical precancer/cancer patients who have undergone hysterectomy are more likely to be diagnosed with subsequent VaIN+ than women without these risk factors who have undergone hysterectomy.29,30 Therefore, the 2019 ASCCP Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors recommend that women who have undergone total hysterectomy for cervical precancer or invasive cervical cancer should undergo surveillance for at least 25 years.31 In 81.0% of hysterectomy cases, the indication for hysterectomy was cervical precancer/cancer. For patients with vaginal cancer, 23.5% had a history of cervical precancer and 70.6% had a history of cervical cancer. These results may be partially explained by the persistence of hrHPV infection in women with prevalent CIN, which is possibly lifelong. Vaginal cancer might develop from VaIN 2/3 before or after hysterectomy with persistent hrHPV infection. However, VaIN 1 is merely an expression of HPV infection and is often transient. Thus, women who underwent hysterectomy for cervical precancer/cancer were at high risk for VaIN 2/3+. Therefore, in our study, for patients who underwent hysterectomy, the rate of VaIN 2/3 vaginal lesions was approximately threefold that of patients who did not undergo hysterectomy (29.5% vs 9.0%; P < 0.001). Careful examination of the vagina during colposcopy before hysterectomy is crucial to exclude VaIN concurrent with cervical precancer/cancer.

The incidence of vaginal cancer was found to be highly age-related in one large study.32 In our study, the mean age of patients with vaginal cancer was 52.5 years, which was 2 years older than those with VaIN 2/3 and almost 7 years older than those with VaIN 1. This suggests that it may take years to progress to VaIN 2/3 and vaginal cancer.

To best of our knowledge, this is the largest retrospective study to investigate cervical screening history, including cytology results, hrHPV results, and colposcopy results, of VaIN+ patients in China. Our data demonstrated that VaIN is not a rare disease. It renewed the acknowledgement of VaIN and attracted the attention of clinical examinations. However, there are two limitations. First, our survey was conducted at a single centre in China, so selection bias is inevitable Second, the patients in our hospital were referred from other hospitals in all of China; thus, we were unable to calculate the prevalence of VaIN in the population.

Conclusion

As the largest OBGYN referral centre in China, the prevalence of VaIN+ has been increasing rapidly since 2013. Although cytology was sensitive (67.5%–76.2%) for detecting vaginal lesions regardless of hysterectomy, cytology combined with hrHPV improve detection accuracy up to 95% in both groups.