Literature DB >> 23452990

Comparison of human papillomavirus testing strategies for triage of women referred with low-grade cytological abnormalities.

David Mesher1, Anne Szarewski1, Louise Cadman1, Janet Austin1, Lesley Ashdown-Barr1, Linda Ho1, George Terry1, Martin Young2, Mark Stoler3, Christine Bergeron4, Julie McCarthy5, Corrina Wright5, Stuart Liddle6, W P Soutter7, Deirdre Lyons8, Jack Cuzick9.   

Abstract

AIM: To compare triage strategies using different human papillomavirus (HPV) consensus and genotyping tests and a p16(INK4a) test.
METHODS: 1228 women referred with a borderline or single mildly dyskaryotic smear. Samples were taken at colposcopy using PreservCyt. Tests included Hybrid Capture 2, Abbott RealTime PCR, BD HPV, Cobas 4800, PreTect HPV-Proofer, APTIMA and p16(INK4a). Results were based on the worst histology within 9 months.
RESULTS: 97/1228 (7.9%) women had CIN3+ (203/1228 (17%) CIN2+). HPV testing alone using Hybrid Capture 2, Abbott RealTime PCR, BD HPV, Cobas 4800 or APTIMA had a sensitivity for CIN3+ ranging from 99.0% to 100.0% and specificity for <CIN2 from 23.3% to 34.7%. p16(INK4a) had a sensitivity of 86.8% and specificity of 50.7%. PreTect HPV-Proofer had a sensitivity of 85.1% and specificity of 73.2%. Testing for HPV type 16 only had sensitivities ranging from 66.0% to 75.5% and specificities from 81.3% to 87.6%. Dual testing with HPV type 16 combined with p16(INK4a) gave a high sensitivity for CIN3+ (78.7% to 98.0%) and specificity for <CIN2 of 58.6% to 81.5%.
CONCLUSIONS: Triage with sensitive HPV testing assays can substantially reduce the number of unnecessary referrals in women with low grade cytology with virtually no loss of sensitivity. Even greater gains can be made if p16 and type 16 are used, but some cases of CIN2 will be missed. In both cases short term surveillance will be needed.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23452990     DOI: 10.1016/j.ejca.2013.01.018

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  8 in total

1.  The Aptima HPV assay fulfills the cross-sectional clinical and reproducibility criteria of international guidelines for human papillomavirus test requirements for cervical screening.

Authors:  D A M Heideman; A T Hesselink; F J van Kemenade; T Iftner; J Berkhof; F Topal; D Agard; C J L M Meijer; P J F Snijders
Journal:  J Clin Microbiol       Date:  2013-08-28       Impact factor: 5.948

2.  The BD Onclarity HPV Assay on Samples Collected in SurePath Medium Meets the International Guidelines for Human Papillomavirus Test Requirements for Cervical Screening.

Authors:  Ditte Ejegod; Fabio Bottari; Helle Pedersen; Maria Teresa Sandri; Jesper Bonde
Journal:  J Clin Microbiol       Date:  2016-06-15       Impact factor: 5.948

3.  The potential of RNA as a target for national screening of pre-cancer.

Authors:  Frank Karlsen; Margaret Muturi; Cosmas Muyabwa; Lars E Roseng; Serge Bigabwa; Byamungu Chihongola; Lucy Muchiri
Journal:  J Public Health Afr       Date:  2018-12-21

Review 4.  Epidemiology of ocular surface squamous neoplasia in Africa.

Authors:  Stephen Gichuhi; Mandeep S Sagoo; Helen A Weiss; Matthew J Burton
Journal:  Trop Med Int Health       Date:  2013-10-30       Impact factor: 2.622

5.  Triage of HR-HPV positive women with minor cytological abnormalities: a comparison of mRNA testing, HPV DNA testing, and repeat cytology using a 4-year follow-up of a population-based study.

Authors:  Maria Persson; K Miriam Elfström; Sophia Brismar Wendel; Elisabete Weiderpass; Sonia Andersson
Journal:  PLoS One       Date:  2014-02-26       Impact factor: 3.240

6.  Disagreement between human papillomavirus assays: an unexpected challenge for the choice of an assay in primary cervical screening.

Authors:  Matejka Rebolj; Sarah Preisler; Ditte Møller Ejegod; Carsten Rygaard; Elsebeth Lynge; Jesper Bonde
Journal:  PLoS One       Date:  2014-01-20       Impact factor: 3.240

7.  Triaging borderline/mild dyskaryotic Pap cytology with p16/Ki-67 dual-stained cytology testing: cross-sectional and longitudinal outcome study.

Authors:  M H Uijterwaal; B I Witte; F J Van Kemenade; D Rijkaart; R Ridder; J Berkhof; G A M A Balfoort-van der Meij; M C G Bleeker; P J F Snijders; C J L M Meijer
Journal:  Br J Cancer       Date:  2014-02-11       Impact factor: 7.640

8.  Clinical and analytical performance of the BD Onclarity™ HPV assay for detection of CIN2+ lesions on SurePath samples.

Authors:  Ditte Møller Ejegod; Jette Junge; Maria Franzmann; Benny Kirschner; Fabio Bottari; Mario Sideri; Maria-Teresa Sandri; Jesper Bonde
Journal:  Papillomavirus Res       Date:  2016-03-02
  8 in total

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