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Evaluation of the diagnostic performance of colposcopy in the detection of cervical high-grade squamous intraepithelial lesions among women with transformation zone type 3

Abstract

Background

Inaccurate colposcopy diagnosis may lead to inappropriate management and increase the incidence of cervical cancer. This study aimed to evaluate the diagnostic accuracy of colposcopy in the detection of histologic cervical intraepithelial neoplasia grade 2 or worse (CIN2+) in women with transformation zone type 3 (TZ3).

Methods

Records from 764 patients with TZ3 who underwent colposcopy-directed biopsy and/or endocervical curettage in Putuo Hospital China between February 2020 and March 2023 were retrospectively collected. Colposcopy was carried out based on 2011 International Federation of Cervical Pathology and Colposcopy (IFCPC) and Colposcopy nomenclature. The diagnostic performance of colposcopy for identifying CIN2 + was evaluated compared with biopsies. The Kappa and McNemar tests were used to perform statistical analyses.

Results

Among the study population, 11.0% had pathologic CIN2+. The relative sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of colposcopy for histologic CIN2 + were 51.2%, 96.5%, 64.2% and 94.1%, respectively. The senior colposcopists (80.6%) had a higher colposcopic accuracy to diagnose histologic CIN2 + than junior colposcopists (68.6%). In subgroup analyses, age group ≥ 60 years (70.3%) showed lowest diagnostic accuracy when compared with age groups of < 45 years (84.4%) and 45–59 years (74.9%).

Conclusion

Our findings suggest an increased risk of diagnostic inaccuracy of colposcopy in identifying CIN2 + in those ≥ 60 years of age with TZ3, and the accuracy of colposcopy is required to be further improved.

Peer Review reports

Introduction

Cervical cancer is the fourth most common cancer in women worldwide, and eighth most common cause of tumor-related mortality in Chinese women, with 119,300 new cases and 59,060 deaths in 2020 [1]. Screening with HPV testing and/or cytology, offers an opportunity to identify women who are at a higher risk of precancerous conditions [2, 3], whereas colposcopy and biopsies are important parts of the diagnostic workup [4]. It has been reported that older women have higher cervical cancer incidence and mortality rates than younger women [5, 6]. Moreover, older women are more commonly diagnosed with advanced-stage disease squamous cell carcinoma and adenocarcinoma) [7] and have a poorer prognosis [8]. This may be due to insufficient screening, screening failure, diagnostic difficulties and insufficient follow-up.

Colposcopy is an indispensable tool for early detection, and accurate use can benefit women by reducing the frequency of unnecessary biopsies, conization surgeries, as well as the frequency of cauterization treatments for cervical erosion [9]. This means, there is a great amount of avoidable stress caused by diagnostic inaccuracies and discrepancies between colposcopic and pathological diagnosis [10]. Many factors can affect colposcopic accuracy, such as colposcopists, skills, screening results, transformation zone (TZ) type and number of biopsies [11, 12]. Management difficulties arise when the TZ is entirely within the endocervical canal, namely transformation zone type 3 (TZ3). Nearly 20% of colposcopic assessments are inadequate due to a TZ3 [13]. Endocervical canal curettage (ECC) which provides fragments of squamous epithelium from inside the cervical canal is generally used in clinical practice for adjunctive biopsy of women with TZ3 at colposcopy [14], and it has been considered should be performed for patients with ASC-H/HSIL cytology, 16/18 HPV infection and those with high-grade colposcopic impressions [15]. Some investigators have reported that adding referral screening results to colposcopic examinations can improve CIN2 + detection, especially for women with TZ3 lesions [16, 17]. Therefore, it remains necessary to identify and assess potential causes of colposcopic inaccuracies and understand diversity and variance in order to reduce unnecessary stress caused and improve outcomes.

The primary aim of this study was to investigate discrepancies between colposcopic and cervical biopsy in women with a TZ3, and the performance of colposcopy for identifying CIN2 + were compared with cervical biopsies.

Materials and methods

Study population

This is a retrospective cohort of women who underwent colposcopic examination as a result of positive screening tests and/or abnormal clinical symptoms between February 2020 and March 2023 at Putuo Hospital, a large tertiary center in Shanghai, China. All women were managed by a select-and-treat approach. If an abnormal TZ was identified, a colposcopy-directed biopsy was performed on the abnormal area. When the TZ was not completely visible or no colposcopic abnormalities were identified, an ECC with a Novak curette was performed, if necessary. Of note, the collection of ECC is not routinely recommended in the guidelines but may be performed depending on the colposcopist,s performance.

The TZ is partially or fully located in the endocervix with no visible squamocolumnar junction (SCJ) corresponding to TZ3. Eligible for inclusion in this study were women who had TZ type 3 according to 2011 International Federation of Cervical Pathology and Colposcopy (IFCPC) and Colposcopy nomenclature [18]. The colposcopists, clinical findings during colposcopy were compared with the final histological results from the punch biopsies and/or endocervical curettage. Women were excluded if they had a hysterectomy or previous excisional treatment for CIN (including cold knife conization, loop electrosurgical excision procedure and cervical laser conization) or received estrogen medical treatment, intended to get pregnant, or underwent follow-up for a previously diagnosed CIN. Moreover, women who underwent colposcopy but had no histologic diagnosis were also excluded. All data, including age, HPV screening result, cytology, indication for colposcopy, TZ types, colposcopic impressions, colposcopist’s level and histological results were recorded prospectively for further research. This study was conducted in accordance with the Declaration of Helsinki and was approved by the Institution Review Board of Putuo Hospital, Shanghai University of Traditional Chinese Medicine. As the retrospective analysis was based on anonymized data, the need for individual informed consent was waived.

HPV and liquid-based cytology testing

HPV DNA testing was performed using the clinically validated cobas@4800 platform (Roche Diagnostic, USA) [19] which detects HPV16, HPV18 and a pool of 12 other high-risk HPV genotypes (HPV31/33/35/39/45/51/52/56/58/59/66/68). Liquid-based cytology was performed by introducing a cervical plastic brush into the external cavity and scraping cells from the exocervix and endocervix, and then placed on a smear slide and fixed. Cytology slide results were classified according to the Bethesda grading system (2014) [20], including no intraepithelial lesions or malignancy (NILM), atypical squamous cells of undetermined significance (ASC-US), low-grade squamous intraepithelial lesion (LSIL), atypical glandular cells of undetermined significance (AGUS), atypical squamous cells cannot exclude high-grade squamous intraepithelial lesion (ASC-H), high-grade squamous intraepithelial lesion (HSIL) or carcinoma.

Colposcopy and histology diagnosis

All colposcopies were performed by gynecologists using an electrionic colposcope (EDAN C6 HD) after preparing the cervix with 5% acetic acid and Lugol’s iodine solution. Colposcopic features assessed in the study included the presence of acetowhite epithelium and its characteristics. The colposcopic diagnostic results according to the 2011 colposcopic terminology of IFCPC included: normal, low-grade lesions, high-grade lesions and suspicious for invasion colposcopic findings [21]. During the period of this retrospective analysis, the team of cervix consisted of 10 colposcopists with various degrees of clinical experience and training. Briefly, colposcopists with more than 10 years of working experience were defined as senior colposcopists, and others were categorized as junior colposcopists. Histopathological outcomes were graded according to World Health Organization (WHO) terminology: normal, cervical intraepithelial neoplasia grade 1 (CIN1), cervical intraepithelial neoplasia grade 2 (CIN2), cervical intraepithelial neoplasia grade 3 (CIN3) and invasive carcinoma [22]. The histopathologic results were taken as the gold standard in the study. When analyzing biopsies and/or endocervical curettage together, the worst grade of lesion was considered as the final histological diagnosis. The accordance was the percentage of women diagnosed by colposcopy and histopathological findings. Over-diagnosis was considered to be present when the histopathological findings are less severe than those obtained during colposcopy. Under-diagnosis was considered to have occurred when histopathological findings highlighted more advanced lesions than colposcopic findings.

Statistical analysis

Descriptive statistics were used to describe clinical characteristics of the study population. The diagnostic performance of colposcopy for detecting CIN2 + was presented in the form of a 2 × 2 table. The agreement between colposcopic findings and histopathological diagnosis was evaluated by Cohen’s kappa (κ) coefficient and Chi-square test at a significance level of 5%. The strength of agreement was judged by the criteria as follows: 0-0.2 as slight, 0.21–0.40 as fair, 041 − 0.60 as moderate, 0.61–0.80 as substantial, and 0.81-1.00 as almost perfect agreement. The exact McNemar’s test was performed to evaluate the diagnostic difference of colposcopy and biopsy to differentiate CIN2+. Relative sensitivity, relative specificity, balanced accuracy, false positive rate (FPR), false negative rate (FNR), positive predictive value (PPV), and negative predictive value (NPV) were used to assess the diagnostic performance of colposcopy for CIN2+. The 95% confidence interval (CI) was estimated. Data analysis was performed using Excel (version 2010) and SPSS software (version 22.0). A p-value < 0.05 was considered statistically significant.

Results

Clinical characteristics of study population

The flowchart selection of study population is depicted in Fig. 1. In total, 764 women with TZ3 who underwent colposcopy-directed biopsy were included in this analysis. Detailed patient characteristics and relevant clinical findings are provided in Table 1. The mean age of the study women was 52.9 ± 11.8 years (range, 20–84 years). Nearly, 77.0% of the patients were 45 years or more of age. Among them, 91 patients (11.9%) had undergone colposcopy due to abnormal clinical signs. Whereas abnormal screening test results (88.1%) remained the most common reason for colposcopy. 724 women (94.8%) had undergone primary HPV screening and 615 (80.5%) women had high-risk genotypes. The most common cytology results were NILM (70.0%), followed by LSIL/ASCUS/AGUS (23.0%) and HSIL+/ASC-H (3.6%). For colposcopy diagnosis, the proportions of low-grade, high-grade and suspicious cancer were 18.2%, 5.6% and 3.2%, respectively. The overall incidence of pathologic CIN2 + in women with TZ3 was 11.0%.

Fig. 1
figure 1

Flowchart illustrating the selection of study population. TZ, transformation zone; LEEP, loop electrosurgical excision procedure; CKC, cold-knife conization; CLC, cervical laser conization; CDB, colposcopy-directed biopsy

Table 1 Description of the study population

Consistency between colposcopic diagnosis and histopathology

We compared the detailed consistency between the colposcopic assessment and the histopathologic results (Fig. 2). The overall concordance rate was 65.6% (501/764). Under-diagnosed cases were observed in 19.8% (151/764). Among 151 under-diagnosed cases, 105 (69.5%), 40 (26.5%), 5 (3.3%), and 1 (0.7%) were finally diagnosed with CIN1, CIN2/3, SqCC and AC, respectively. Specifically, among 139 cases that had been diagnosed with low-grade impressions by colposcopy, 16 cases (11.5%) were correctly diagnosed with CIN2/3 and 1 case (0.7%) with SqCC.

Fig. 2
figure 2

Comparison of results between colposcopic findings and histology. CIN1, cervical intraepithelial neoplasia grade 1; CIN2, cervical intraepithelial neoplasia grade 2; CIN3, cervical intraepithelial neoplasia grade 3; SqCC, squamous cell carcinoma; AC, adenocarcinoma

Diagnostic performance of colposcopy in the detection of CIN2+

Considering the histologic results as the gold standard, we evaluated the diagnostic performance of colposcopy for identifying CIN2 + with the following results: relative sensitivity, 51.2%; relative specificity, 96.5%; balanced accuracy, 73.8%; PPV, 64.2% and NPV, 94.1% (Fig. 3). Cohen’s κ coefficient for colposcopy and biopsy was 0.523, indicating moderate agreement. However, the exact McNemar’s test revealed that colposcopy was significantly different in the diagnosis of CIN2 + when compared to biopsy in all women with TZ3 (p = 0.047). We also performed subgroup analysis according to colposcopists, experience. Cohen’s κ coefficients for colposcopy and biopsy in subgroup of junior and senior colposcopists were 0.399 (fair agreement) and 0.685 (substantial agreement), respectively. The specificity between senior and junior colposcopists was comparable. Whereas, the relative sensitivity of senior (63.2%) was higher than junior (41.3%) colposcopists (Table 2).

Fig. 3
figure 3

Diagnostic performance of colposcopy in patients with TZ3.(A) 2 × 2 contingency table, (B) value for each parameter.TZ, transformation zone; CIN, cervical intraepithelial neoplasia; SqCC, squamous cell carcinoma; AC, adenocarcinoma

Table 2 Diagnostic performance of colposcopy in detecting CIN2 + among patients with transformation zone type 3

Age-specific subgroup analysis

The performance of colposcopy in the detection of histologic CIN2 + in different age groups is shown in Fig. 4. In the younger group < 45 years, the diagnostic performance of colposcopy for identifying CIN2 + was as follows: relative sensitivity, 70.0%; relative specificity, 98.8%; balanced accuracy, 84.4%; PPV, 77.8% and NPV, 98.2% (Fig. 4AB). Cohen’s κ coefficient for colposcopy and biopsy was 0.721, indicating substantial agreement. The overall rates for under-, correctly- and over-diagnosed cases were 16.5%, 72.2% and 11.3%, respectively (Table 3).

Fig. 4
figure 4

Diagnostic performance of colposcopy in age-specific subgroups including patients aged < 45 years, 45–59 years, and ≥ 60 years. (A, C, E) 2 × 2 contingency table, (B, D, F) value for each parameter. TZ, transformation zone; CIN, cervical intraepithelial neoplasia; SqCC, squamous cell carcinoma; AC, adenocarcinoma

Table 3 Diagnostic accuracy of colposcopy according to the patients’ age group

In the middle subgroup of patients aged 45–59 years, the diagnostic performance of colposcopy for identifying CIN2 + was as follows: relative sensitivity, 53.6%; relative specificity, 96.2%; balanced accuracy, 74.9%; PPV, 57.7% and NPV, 95.6% (Fig. 4CD). Cohen’s κ coefficient for colposcopy and biopsy was 0.513, indicating moderate agreement. The overall rates for under-, correctly- and over-diagnosed cases were 21.2%, 63.2% and 15.6%, respectively (Table 3).

In the older group ≥ 60 years, the diagnostic performance of colposcopy for identifying CIN2 + was as follows: relative sensitivity, 45.7%; relative specificity, 95.0%; balanced accuracy, 70.3%; PPV, 65.6% and NPV, 89.3% (Fig. 4EF). Cohen’s κ coefficients for colposcopy and biopsy was 0.462, indicating moderate agreement. The overall rates for under-, correctly- and over-diagnosed cases were 20.3%, 64.0% and 15.7%, respectively (Table 3).

Discussion

This cross-sectional study included 764 colposcopies with histology. The risk of CIN2 + among these patients with TZ3 was 11.0%. The diagnostic accuracy in the detection of histologic CIN2 + in women with TZ3 is quite challenging, particularly in the elderly. Women with TZ3 were the most commonly encountered among women older than 50 years (70%) in a prospective multicenter study by Luyten et al. [23]. squamocolumnar junction may be invisible in perimenopausal women, and cervical lesions may extend into the endocervical canal, thus rendering colposcopic examination unsatisfactory. A recent observational study conducted in Denmark also revealed that most women (74.9%) have TZ3 at colposcopy, and 20.0% of women had CIN2 + diagnosed among women aged ≥ 69 referred to colposcopy due to an HPV-positive screening test. The findings also suggested a potential risk of underdiagnosis of CIN2 + in older postmenopausal women referred to colposcopy [24]. Additionally, Gustafson et al. [11] found that CIN2 + detection is underestimated when comparing the proportion of CIN2 + in cervical biopsies with that in large loop excision of the transformation zone (LLETZ) specimens in women aged ≥ 45 years with TZ3.

In this study, Our results revealed a relatively lower balanced accuracy (73.8%), relative sensitivity (51.2%), and raise specificity (96.5%) when CIN2 + as the threshold, which was comparable to studies reported in Bangladesh by Ara et al. (sensitivity, 50%; specificity, 94.0%) [25] and in China by Ruan et al. (sensitivity, 56.29%; specificity, 93.82%) [26]. A similar study conducted in Bhutan found the sensitivity of colposcopy to detect CIN2 + was 66.67%, and accuracy was 73.73% [27]. In a study also done in China, the sensitivity, specificity, and accuracy of colposcopy to diagnose histologic CIN2 + were 70.2%, 75.1% and 72.9%, respectively [16]. A recent meta-analysis showed that colposcopic accuracy for detecting CIN2 + was 89%, with combined sensitivity and specificity were 68% and 93%, respectively [28]. The sensitivity of colposcopic impressions ranged from 29 to 100% and the specificity from 12 to 88% based on 11 studies [29].

Colposcopy is a highly subjective examination method, the performance of colposcopy in cervical pathological diagnosis varies greatly among observers, which depends on the duration of the experience of colposcopists [27]. In our previous study, the diagnostic performance of colposcopy in the diagnosis of CIN2 + by senior and junior colposcopists was comparable in women with oncogenic HPV regardless of TZ type [30]. However, herein subgroup according to colposcopists, experience, we found the relative sensitivity (63.2% versus 41.3%) and accuracy (80.6% versus 68.6%) of senior colposcopists to identify CIN2 + were significantly higher than those of junior colposcopists. The specificity (98.0% versus 95.8%) of seniors was slightly higher than juniors. Dorji et al. [27] also found the sensitivity (80.00% versus 59.46%) of senior colposcopists was higher than junior colposcopists. However, senior colposcopists had lower specificity (71.07% versus 76.72%) and almost comparable accuracy (72.60% versus 72.55%). In a similar study done in Germany, the colposcopic sensitivity (86.0% versus 70.2%) of senior colposcopists to diagnose CIN2 + lesions was higher than junior colposcopists, with lower specificity (65.1% versus 68.6%) [31]. One possible explanation might be the fact that young colposcopists lack of course and some amount of knowledge and skills acquired over the years. Our data underline the need for qualified staff including standardized colposcopy steps, regular updated courses, regular supervision and quality assurance measures, especially for junior colposcopists.

In subgroup analysis according to patients, age, we found the diagnostic accuracy of colposcopy for identifying CIN2 + decreased as age increased with the balanced accuracy of colposcopy in age group < 45 years, 45–59 years and ≥ 60 years being 84.4%, 74.9% and 70.3%, respectively. A recent retrospective study reported the accuracy rates for detecting HSIL which were 65.67% (age ≤ 30 years ), 71.12% (31–45 years) and 60.43% (> 45 years) [32]. Some studies have also observed that the diagnostic accuracy of colposcopy-guided biopsy for identifying HSIL + decreased with increasing age. For example, Kim et al. [33] found that the diagnostic accuracy of colposcopy-guided biopsy in age groups < 35 years was 81.0%, 74.4% for 35–50 years and 68.8% for those patients aged ≥ 50 years. Stuebs et al. [17] also reported similar trends in the accuracy rates for detecting HSILs. The authors themselves postulated that relatively poor diagnostic performance for identifying HSIL + in women ≥ 50 years might be related to postmenopause, unidentifiable SCJ or cervical lesions that are not well visualized with colposcopy. CIN2 + cases were more likely to be missed among older women and therefore should be considered more carefully during clinical consultations.

A major strength of this study was the use of real-world data from a number of women with TZ3 at colposcopy. Our study contributed results from a highly unique group of women attending colposcopy which provided baseline data, and way forward for improvement. However, there are several limitations that should be considered. First, although we selected consecutive patients with clearly defined eligibility criteria, inevitable issues might arise in retrospective studies such as selection bias. For example, women with TZ3 but without histology diagnosis were excluded, which will yield inherent bias. Second, as a single-institution study, the sample size might be insufficient, and larger numbers are needed to make the results more robust. Third, the biopsy specimens were taken only from suspicious lesions without comparable control specimens. Finally, we have only studied colposcopic accuracy for detecting CIN2+, the data required to discern differences between CIN2+, CIN3 + and cervical cancer are also meaningful.

Conclusions

In conclusion, the overall diagnostic accuracy of colposcopy and the consistency between colposcopy and histology in our study were comparable to previous studies, but further improvement was required. The relative sensitivity and balanced accuracy among junior colposcopists were lower than senior colposcopists. Moreover, diagnostic inaccuracies of colposcopy were magnified in those ≥ 60 years old. Future measures towards improving the performance of colposcopy such as using a reasonable scoring system and standard diagnostic criteria are still warranted.

Data availability

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

References

  1. Zheng R, Zhang S, Zeng H, Wang S, Sun K, Chen R, Li L, Wei W, He J. Cancer incidence and mortality in China, 2016. J Natl Cancer C. 2022;2(1):1–9.

    Article  Google Scholar 

  2. Kjær SK, Frederiksen K, Munk C, Iftner T. Long-term absolute risk of cervical intraepithelial neoplasia grade 3 or worse following human papillomavirus infection: role of persistence. J Natl Cancer I. 2010;102(19):1478–88.

    Article  Google Scholar 

  3. Castle PE, Rodríguez AC, Burk RD, Herrero R, Wacholder S, Alfaro M, Morales J, Guillen D, Sherman ME, Solomon D. Short term persistence of human papillomavirus and risk of cervical precancer and cancer: population based cohort study. BMJ. 2009;339:b2569.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Wentzensen N, Walker JL, Gold MA, Smith KM, Zuna RE, Mathews C, Dunn ST, Zhang R, Moxley K, Bishop E. Multiple biopsies and detection of cervical cancer precursors at colposcopy. J Clin Oncol. 2015;33(1):83.

    Article  PubMed  Google Scholar 

  5. Hammer A, Kahlert J, Gravitt PE, Rositch AF. Hysterectomy-corrected cervical cancer mortality rates in Denmark during 2002‐2015: a registry‐based cohort study. Acta Obstet Gyn Scan. 2019;98(8):1063–9.

    Article  Google Scholar 

  6. Hammer A, Kahlert J, Rositch A, Pedersen L, Gravitt P, Blaakaer J, Soegaard M. The temporal and age-dependent patterns of hysterectomy‐corrected cervical cancer incidence rates in Denmark: a population‐based cohort study. Acta Obstet Gyn Scan. 2017;96(2):150–7.

    Article  Google Scholar 

  7. Liu Q, Zhou X, Zhang X, Strickland AL, Zheng W, Chen H, Zhou F. HPV genotype specific and age stratified immediate prevalence of cervical precancers and cancers in women with NILM/hrHPV+: a single center retrospective study of 26,228 cases. Cancer Manag Res. 2021; 6869–77.

  8. Darlin L, Borgfeldt C, Widén E, Kannisto P. Elderly women above screening age diagnosed with cervical cancer have a worse prognosis. Anticancer Res. 2014;34(9):5147–51.

    PubMed  Google Scholar 

  9. Fan A, Wang C, Zhang L, Yan Y, Han C, Xue F. Diagnostic value of the 2011 International Federation for Cervical Pathology and Colposcopy Terminology in predicting cervical lesions. Oncotarget. 2018;9(10):9166–76.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Massad LS, Collins YC. Strength of correlations between colposcopic impression and biopsy histology. Gynecol Oncol. 2003;89(3):424–8.

    Article  PubMed  Google Scholar 

  11. Gustafson LW, Hammer A, Bennetsen MH, Kristensen CB, Majeed H, Petersen LK, Andersen B, Bor P. Cervical intraepithelial neoplasia in women with transformation zone type 3: cervical biopsy versus large loop excision. BJOG-An Int J Obstet Gy. 2022;129(13):2132–40.

    Article  Google Scholar 

  12. Ren H, Jia M, Zhao S, Li H, Fan S. Factors correlated with the accuracy of colposcopy-directed biopsy: a systematic review and meta-analysis. J Invest Surg. 2022;35(2):284–92.

    Article  PubMed  Google Scholar 

  13. Massad LS, Einstein MH, Huh WK, Katki HA, Kinney WK, Schiffman M, Solomon D, Wentzensen N, Lawson HW. 2012 updated consensus guidelines for the management of abnormal cervical cancer screening tests and cancer precursors. J Low Genit Tract Di. 2013;17:S1–27.

    Article  Google Scholar 

  14. Liu AH, Walker J, Gage JC, Gold MA, Zuna R, Dunn ST, Schiffman M, Wentzensen N. Diagnosis of cervical precancers by endocervical curettage at colposcopy of women with abnormal cervical cytology. Obstet Gynecol. 2017;130(6):1218.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Wei B, Li Q, Seery S, Qiao Y, Jiang Y. Endocervical curettage for diagnosing high-grade squamous intraepithelial lesions or worse in women with type 3 transformation zone lesions: a retrospective, observational study. BMC Womens Health. 2023;23(1):1–9.

    Article  Google Scholar 

  16. Wei B, Zhang B, Xue P, Seery S, Wang J, Li Q, Jiang Y, Qiao Y. Improving colposcopic accuracy for cervical precancer detection: a retrospective multicenter study in China. BMC Cancer. 2022;22(1):388.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Stuebs FA, Schulmeyer CE, Mehlhorn G, Gass P, Kehl S, Renner SK, Renner SP, Geppert C, Adler W, Hartmann A. Accuracy of colposcopy-directed biopsy in detecting early cervical neoplasia: a retrospective study. Arch Gynecol Obstet. 2019;299:525–32.

    Article  PubMed  Google Scholar 

  18. Quaas J, Reich O, Küppers V. Explanation and use of the Rio 2011 colposcopy nomenclature of the IFCPC (International Federation for Cervical Pathology and Colposcopy). Geburtsh Frauenheilk. 2014;74(12):1090–2.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Heideman D, Hesselink A, Berkhof J, Van Kemenade F, Melchers W, Daalmeijer NF, Verkuijten M, Meijer C, Snijders P. Clinical validation of the cobas 4800 HPV test for cervical screening purposes. J Clin Microbiol. 2011;49(11):3983–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Solomon D, Davey D, Kurman R, Moriarty A, O’Connor D, Prey M, Raab S, Sherman M, Wilbur D, Wright T Jr. The 2001 Bethesda System: terminology for reporting results of cervical cytology. JAMA. 2002;287(16):2114–9.

    Article  PubMed  Google Scholar 

  21. Bornstein J, Bentley J, Bösze P, Girardi F, Haefner H, Menton M, Perrotta M, Prendiville W, Russell P, Sideri M. 2011 colposcopic terminology of the International Federation for Cervical Pathology and Colposcopy. Obst Gynecol. 2012;120(1):166–72.

    Article  Google Scholar 

  22. Richart RM. Natural history of cervical intraepithelial neoplasia. Clin Obstet Gynecol. 1967;10(4):748–84.

    Article  Google Scholar 

  23. Luyten A, Buttmann-Schweiger N, Hagemann I, Scherbring S, Boehmer G, Gieseking F, Woelber L, Glasenapp F, Hampl M, Kuehler-Obbarius C. Utility and reproducibility of the international federation for cervical pathology and colposcopy classification of transformation zones in daily practice: a multicenter study of the German colposcopy network. J Low Genit Tract Di. 2015;19(3):185–8.

    Article  Google Scholar 

  24. Booth BB, Tranberg M, Gustafson LW, Christiansen AG, Lapirtis H, Krogh LM, Hjorth IMD, Hammer A. Risk of cervical intraepithelial neoplasia grade 2 or worse in women aged ≥ 69 referred to colposcopy due to an HPV-positive screening test. BMC Cancer. 2023;23(1):405.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Ara R, Khatun S, Pervin S, Jahan M, Shahera U, Ferdous J, Begum SA, Fatema S, Begum M, Nazneen S. Role of molecular biomarker human papilloma virus (HPV) E6 oncoprotein in cervical cancer screening. Gynaecol Oncol. 2020;158(3):590–6.

    Article  CAS  Google Scholar 

  26. Ruan Y, Liu M, Guo J, Zhao J, Niu S, Li F. Evaluation of the accuracy of colposcopy in detecting high-grade squamous intraepithelial lesion and cervical cancer. Arch Gynecol Obstet. 2020;302:1529–38.

    Article  PubMed  Google Scholar 

  27. Dorji N, Tshering S, Choden S, Chhetri M, Bhujel D, Wangden T, Pradhan B, Bhutia PC, Tshomo U. Evaluation of the diagnostic performance of colposcopy in the diagnosis of histologic cervical intraepithelial neoplasia 2+(CIN2+). BMC Cancer. 2022;22(1):930.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Qin D, Bai A, Xue P, Seery S, Wang J, Mendez MJG, Li Q, Jiang Y, Qiao Y. Colposcopic accuracy in diagnosing squamous intraepithelial lesions: a systematic review and meta-analysis of the International Federation of Cervical Pathology and Colposcopy 2011 terminology. BMC Cancer. 2023;23(1):187.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Mustafa RA, Santesso N, Khatib R, Mustafa AA, Wiercioch W, Kehar R, Gandhi S, Chen Y, Cheung A, Hopkins J, et al. Systematic reviews and meta-analyses of the accuracy of HPV tests, visual inspection with acetic acid, cytology, and colposcopy. Int J Gynecol Obstet. 2016;132(3):259–65.

    Article  Google Scholar 

  30. Li X, Xiang F, Zhao Y, Li Q, Gu Q, Zhang X, Chen Z, Zhang M, Wang J, Liu R, Kang X, Wu R. Detection of cervical high-grade squamous intraepithelial lesions and assessing diagnostic performance of colposcopy among women with oncogenic HPV. BMC Womens Health. 2023;23(1):1–8.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Stuebs FA, Dietl AK, Behrens A, Adler W, Geppert C, Hartmann A, Knöll A, Beckmann MW, Mehlhorn G, Schulmeyer CE. Concordance rate of colposcopy in detecting cervical intraepithelial lesions. Diagnostics. 2022;12(10):2436.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Bai A, Wang J, Li Q, Seery S, Xue P, Jiang Y. Assessing colposcopic accuracy for high-grade squamous intraepithelial lesion detection: a retrospective, cohort study. BMC Womens Health. 2022;22(1):1–8.

    Article  Google Scholar 

  33. Kim SI, Kim SJ, Suh DH, Kim K, No JH, Kim YB. Pathologic discrepancies between colposcopy-directed biopsy and loop electrosurgical excision procedure of the uterine cervix in women with cytologic high-grade squamous intraepithelial lesions. J Gynecol Oncol. 2020;31(2):e13.

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors would like to thank Putuo Hospital for the support.

Funding

This work was funded by Science and Technology Innovation Project of Putuo District Health System (No. ptkwws202305, No. ptkwws202307), the One Hundred Talents Project of Putuo Hospital, Shanghai University of Traditional Chinese Medicine (No. 2022-RCQH-03).

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Authors

Contributions

XL and YZ planned and designed the study; XL and FX drafted this manuscript; XZ and ZC collected the data; MZ performed the statistical analysis; XK and RW contributed a lot to the design of this study. All authors have read and approved the final version of the manuscript.

Corresponding authors

Correspondence to Xiangdong Kang or Rong Wu.

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Ethics approval and consent to participate

This study was approved by the Institutional Review Board of Putuo Hospital, Shanghai University of Traditional Chinese Medicine (No. PTEC-A-2020-24-3). All methods were performed in accordance with the Declaration of Helsinki. The need for informed consent was waived by the IRB of Putuo Hospital due to the retrospective nature of archived datasets and fully anonymized personal information.

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Not applicable.

Competing interests

The authors declare no competing interests.

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Li, X., Zhao, Y., Xiang, F. et al. Evaluation of the diagnostic performance of colposcopy in the detection of cervical high-grade squamous intraepithelial lesions among women with transformation zone type 3. BMC Cancer 24, 381 (2024). https://doi.org/10.1186/s12885-024-12156-2

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