Clinical impact of age-specific distribution of combination patterns of cytology and high-risk HPV status on cervical intraepithelial neoplasia grade 2 or more

被引:3
|
作者
Sakai, Mie [1 ,2 ]
Ohara, Tsutomu [1 ,3 ]
Suzuki, Haruka [1 ,3 ]
Kadomoto, Tatsuki [1 ]
Inayama, Yoshihide [1 ,3 ]
Shitanaka, Shimpei [1 ,3 ]
Sumitomo, Masahiro [1 ]
Matsumura, Noriomi [4 ]
Yamanoi, Koji [1 ,3 ]
机构
[1] Toyooka Publ Hosp, Dept Obstet & Gynecol, Toyooka, Hyogo 6638501, Japan
[2] Shiga Gen Hosp, Dept Obstet & Gynecol, Moriyama, Shiga 5248524, Japan
[3] Kyoto Univ, Dept Obstet & Gynecol, Grad Sch Med, 54,Shogoinkawahara Cho, Kyoto 6068507, Japan
[4] Kindai Univ, Dept Obstet & Gynecol, Grad Sch Med, Osakasayama, Osaka 5898511, Japan
关键词
human papillomavirus; cytology; cervical intraepithelial neoplasia; squamous cell carcinoma; cervical cancer; human papillomavirus vaccine; CANCER; MORTALITY; INFECTIONS; PREVALENCE;
D O I
10.3892/ol.2023.13970
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To the best of our knowledge, the present study is the first to elucidate the significance of cytology and high-risk human papillomavirus (hrHPV) status in different age groups for the detection of cervical intraepithelial neoplasia (CIN)2, CIN3 and squamous cell carcinoma (SCC). There were 12 combinations based on cytology and hrHPV status [cytology: Atypical squamous cells (ASC) of undetermined significance, low-grade squamous intraepithelial lesion, ASC not excluding high-grade squamous intraepithelial lesion (HSIL) and HSIL; hrHPV status: HPV16/18-positive (16/18+), hrHPV positive for subtypes other than 16/18 (others+) and hrHPV-negative (hrHPV-)]. All patients were categorized into four groups based on age (18-29, 30-39, 40-49 and & GE;50 years). For patients with CIN2, CIN3 and SCC (CIN2+) (n=107), the distribution of cytology and hrHPV was investigated in each age group. In addition, for all patients (n=446), the occurrence of CIN2+ in each of the 12 combinations was investigated in each age group. In the 18-29-year age group, the most common combination was HSIL and 16/18+, followed by HSIL and others+, which accounted for 73% of CIN2+ cases. The occurrence of HSIL and 16/18+ decreased with increasing age, and no cases occurred in the 50-year age group. In the 18-29-year age group, all patients with HSIL and 16/18+ were diagnosed with CIN2+. CIN2+ was predominantly detected in patients with HSIL in the 18-29-year age group, as well as hrHPV- and others+. This definite distinction was not observed in any other age group. For CIN2+, the distribution patterns of cytology and hrHPV status combinations varied significantly among different age groups. Accordingly, the clinical impact of the combination of cytological findings and hrHPV status can vary among age groups.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Screening for high-grade cervical intra-epithelial neoplasia and cancer by testing for high-risk HPV, routine cytology or colposcopy
    Schneider, A
    Hoyer, H
    Lotz, B
    Leistritz, S
    Kühne-Heid, R
    Nindl, I
    Müller, B
    Haerting, J
    Durst, M
    INTERNATIONAL JOURNAL OF CANCER, 2000, 89 (06) : 529 - 534
  • [22] Cigarette smoking and high-risk HPV DNA as predisposing factors for high-grade cervical intraepithelial neoplasia (CIN) in young Brazilian women
    Roteli-Martins, CM
    Panetta, K
    Alves, VAF
    Siqueira, SAC
    Syrjanen, KJ
    Derchain, SFM
    ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1998, 77 (06) : 678 - 682
  • [23] Risk of high-grade cervical intra-epithelial neoplasia based on cytology and high-risk HPV testing at baseline and at 6-months
    Bulk, Saskia
    Bulkmans, Nicole W. J.
    Berkhof, Johannes
    Rozendaal, Lawrence
    Boeke, A. Joan P.
    Verheijen, Rene H. M.
    Snijders, Peter J. F.
    Meijer, Chris J. L. M.
    INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (02) : 361 - 367
  • [24] Impact of postsurgical vaginal microbiome on high-risk HPV infection and recurrence risk in patients with cervical cancer and intraepithelial neoplasia: A retrospective study
    Ma, Yan
    Wan, Lijuan
    Li, Ruonan
    Chen, Xixi
    Wang, Huiyan
    GYNECOLOGIC ONCOLOGY REPORTS, 2024, 55
  • [25] Dynamic characteristics of high-risk HPV infection in women with low-grade cervical intraepithelial neoplasia, based on a community longitudinal study
    Zhao, Kailu
    Li, Huimin
    Cui, Meng
    Song, Li
    Lyu, Yuanjing
    Ding, Ling
    Wang, Jintao
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2025, 44 (03) : 671 - 679
  • [26] Association between vaginal microflora, high-risk hpv infection and hpv e6/e7 expression in high grade cervical intraepithelial neoplasia
    Plisko, O.
    Zodzika, J.
    Jermakova, I.
    Rezeberga, D.
    Kroica, J.
    Liepniece-Karele, I.
    Araja, D.
    Kunicina, D.
    Prusakevica, A.
    EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2022, 270 : E31 - E31
  • [27] The impact of age and high-risk human papillomavirus (hrHPV) status on the prevalence of high-grade cervical intraepithelial neoplasia (CIN2+) in women with persistent hrHPV-positive, cytology-negative screening samples: a prospective cohort study
    Tidy, J. A.
    Lyon, R.
    Ellis, K.
    Macdonald, M.
    Palmer, J. E.
    BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2020, 127 (10) : 1260 - 1267
  • [28] Low grade squamous intraepithelial lesion (LSIL) and high risk HPV status: Effect of age on follow-up with high grade cervical lesions
    Ko, V.
    Tambouret, R. H.
    Wilbur, D. C.
    LABORATORY INVESTIGATION, 2007, 87 : 73A - 74A
  • [29] Low grade squamous intraepithelial lesion (LSIL) and high risk HPV status: Effect of age on follow-up with high grade cervical lesions
    Ko, V.
    Tambouret, R. H.
    Wilbur, D. C.
    MODERN PATHOLOGY, 2007, 20 : 73A - 74A
  • [30] Role of high-risk human papillomavirus (HPV) mRNA testing in the prediction of residual disease after conisation for high-grade cervical intraepithelial neoplasia
    Trope, Ameli
    Jonassen, Christine M.
    Sjoborg, Katrine D.
    Nygard, Mari
    Dahl, Fredrik A.
    Alfsen, G. Cecilie
    Lie, A. Kathrine
    GYNECOLOGIC ONCOLOGY, 2011, 123 (02) : 257 - 262