Literature DB >> 15751045

Triage using HPV-testing in persistent borderline and mildly dyskaryotic smears: proposal for new guidelines.

Aagje G Bais1, Matejka Rebolj, Peter J F Snijders, Frits A de Schipper, Dries A J van der Meulen, René H M Verheijen, Feja Voorhorst, Marjolein van Ballegooijen, Chris J L M Meijer, Theo J M Helmerhorst.   

Abstract

In the Netherlands 2% of cervical smears in the cervical cancer screening program are read as borderline or mildly dyskaryotic cytology (BMD smear). Only in about 10% of these women a high-grade CIN lesion (CIN II-III) is present; therefore referral is for the majority unnecessary. In our study triage with high-risk HPV (hrHPV) testing was used to identify women at risk for development of high-grade CIN lesions after a repeat BMD smear. A "wait-and-see" period was incorporated allowing clearance of HPV and regression of the lesion. Women with a low-grade lesion, irrespective of their HPV status, were monitored at 12 months; women with a high-grade lesion were monitored at 6 and 12 months. Fifty-one of the 105 women (49%) were hrHPV negative at baseline; none of them showed progression of the lesion within the first year of follow-up (NPV 100%). High-grade CIN was present in 1 patient who was HPV negative at baseline (2%); she demonstrated regression after 12 months. Nineteen of the hrHPV positive women (35%) demonstrated a high-grade CIN lesion at baseline and 3 cleared hrHPV after 6 months, with a subsequent regression of CIN. Ten women remained hrHPV positive with persistence of high-grade CIN and were eventually treated. At baseline, 35 hrHPV positive women demonstrated a low-grade lesion, 19 remained hrHPV positive after 12 months and 5 developed high-grade CIN. Sixteen out of the 35 cleared the hrHPV infection without progression of the lesion. In conclusion, triage, using hrHPV testing for women with persistent BMD cytology, can select women who are not at risk for development of high-grade CIN. We recommend return to the screening program without referral for colposcopic examination if hrHPV is absent. For hrHPV positive women, a repeat hrHPV test after another 6 months is suggested. Referral is only required if persistence of hrHPV is established. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15751045     DOI: 10.1002/ijc.20958

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  9 in total

1.  Cytology and human papillomavirus testing 6 to 12 months after ASCUS or LSIL cytology in organized screening to predict high-grade cervical neoplasia between screening rounds.

Authors:  Ameli Tropé; Katrine D Sjøborg; Mari Nygård; Kjetil Røysland; Suzanne Campbell; G Cecilie Alfsen; Christine M Jonassen
Journal:  J Clin Microbiol       Date:  2012-04-18       Impact factor: 5.948

2.  Agreement between the AMPLICOR Human Papillomavirus Test and the Hybrid Capture 2 assay in detection of high-risk human papillomavirus and diagnosis of biopsy-confirmed high-grade cervical disease.

Authors:  Francesca Carozzi; Simonetta Bisanzi; Cristina Sani; Marco Zappa; Silvia Cecchini; Stefano Ciatto; Massimo Confortini
Journal:  J Clin Microbiol       Date:  2006-11-22       Impact factor: 5.948

3.  Agreement for HPV genotyping detection between self-collected specimens on a FTA cartridge and clinician-collected specimens.

Authors:  Yaoyao Guan; Patti E Gravitt; Roslyn Howard; Yolanda J Eby; Shaoming Wang; Belinda Li; Changyan Feng; You-Lin Qiao; Philip E Castle
Journal:  J Virol Methods       Date:  2013-01-29       Impact factor: 2.014

Review 4.  Persistent human papillomavirus infection and cervical neoplasia: a systematic review and meta-analysis.

Authors:  Jill Koshiol; Lisa Lindsay; Jeanne M Pimenta; Charles Poole; David Jenkins; Jennifer S Smith
Journal:  Am J Epidemiol       Date:  2008-05-15       Impact factor: 4.897

5.  Detection and genotyping of human papillomavirus in self-obtained cervicovaginal samples by using the FTA cartridge: new possibilities for cervical cancer screening.

Authors:  Charlotte H Lenselink; Roosmarie P de Bie; Dennis van Hamont; Judith M J E Bakkers; Wim G V Quint; Leon F A G Massuger; Ruud L M Bekkers; Willem J G Melchers
Journal:  J Clin Microbiol       Date:  2009-06-24       Impact factor: 5.948

6.  Comparison of the DiagCor GenoFlow Human Papillomavirus Array Test and Roche Linear Array HPV Genotyping Test.

Authors:  Fiona K Y Wong; Johannes C Y Ching; Joseph K F Chow
Journal:  Open Virol J       Date:  2010-11-03

7.  Long-term CIN3+ risk in women with abnormal cytology; role of hrHPV testing.

Authors:  M Kocken; J Berkhof; F J van Kemenade; J A Louwers; A Zaal; M A E Nobbenhuis; G Kenter; P J F Snijders; C J L M Meijer; T J M Helmerhorst
Journal:  Br J Cancer       Date:  2012-02-14       Impact factor: 7.640

8.  Guidelines of the Italian Society for Virology on HPV testing and vaccination for cervical cancer prevention.

Authors:  Luisa Barzon; Colomba Giorgi; Franco M Buonaguro; Giorgio Palù
Journal:  Infect Agent Cancer       Date:  2008-12-16       Impact factor: 2.965

9.  Triage of women with equivocal or low-grade cervical cytology results: a meta-analysis of the HPV test positivity rate.

Authors:  Marc Arbyn; Pierre Martin-Hirsch; Frank Buntinx; Marc Van Ranst; Evangelos Paraskevaidis; Joakim Dillner
Journal:  J Cell Mol Med       Date:  2009-01-23       Impact factor: 5.310

  9 in total

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