Follow-up after treatment of high-grade cervical dysplasia: The utility of six-month colposcopy and cytology and routine 12-month colposcopy.


Journal

The Australian & New Zealand journal of obstetrics & gynaecology
ISSN: 1479-828X
Titre abrégé: Aust N Z J Obstet Gynaecol
Pays: Australia
ID NLM: 0001027

Informations de publication

Date de publication:
12 2020
Historique:
received: 04 11 2019
accepted: 09 08 2020
pubmed: 17 9 2020
medline: 16 2 2021
entrez: 16 9 2020
Statut: ppublish

Résumé

Australian Cervical Screening Program guidelines no longer recommend colposcopy and cytology at six months following treatment of cervical intraepithelial neoplasia (CIN2/3) and a co-test of cure can be performed at 12 months without colposcopy. To determine the usefulness of six-month colposcopy and cytology and routine colposcopy with co-testing at 12 months in detecting persistent or recurrent disease in patients treated for CIN2/3. We conducted a review of all patients with histologically proven CIN2/3 who underwent a cervical excisional procedure between March 2012 and March 2017 in one specialised centre. We examined 1215 cases and 750 remained after exclusions for analysis. At six months (722 cases, 96.2%) seven of 42 (16.7%) patients with high-grade cytology had a high-grade colposcopy and 24 of 42 (57.1%) had a normal colposcopy. Persistent CIN2/3 was diagnosed in 12 cases (1.7%) and only 1/3 had a high-grade colposcopy. Cytology was more useful than colposcopy in detecting persistent disease. At 12 months (638 cases, 85%) routine colposcopy at the time of co-testing had a high false positive rate with all high-grade changes negative on biopsy and co-test. Recurrent CIN2/3 was diagnosed in five cases, and four had normal colposcopy at co-testing. There may be a delay in detection of persistent/recurrent CIN2/3 in a small number of cases without six-month colposcopy and cytology; however, it is not likely to negatively impact overall clinical outcome. Co-testing at 12 months following treatment of CIN2/3 without colposcopy is safe and routine colposcopy at collection of the co-test can be omitted.

Sections du résumé

BACKGROUND
Australian Cervical Screening Program guidelines no longer recommend colposcopy and cytology at six months following treatment of cervical intraepithelial neoplasia (CIN2/3) and a co-test of cure can be performed at 12 months without colposcopy.
AIMS
To determine the usefulness of six-month colposcopy and cytology and routine colposcopy with co-testing at 12 months in detecting persistent or recurrent disease in patients treated for CIN2/3.
MATERIALS AND METHODS
We conducted a review of all patients with histologically proven CIN2/3 who underwent a cervical excisional procedure between March 2012 and March 2017 in one specialised centre.
RESULTS
We examined 1215 cases and 750 remained after exclusions for analysis. At six months (722 cases, 96.2%) seven of 42 (16.7%) patients with high-grade cytology had a high-grade colposcopy and 24 of 42 (57.1%) had a normal colposcopy. Persistent CIN2/3 was diagnosed in 12 cases (1.7%) and only 1/3 had a high-grade colposcopy. Cytology was more useful than colposcopy in detecting persistent disease. At 12 months (638 cases, 85%) routine colposcopy at the time of co-testing had a high false positive rate with all high-grade changes negative on biopsy and co-test. Recurrent CIN2/3 was diagnosed in five cases, and four had normal colposcopy at co-testing.
CONCLUSIONS
There may be a delay in detection of persistent/recurrent CIN2/3 in a small number of cases without six-month colposcopy and cytology; however, it is not likely to negatively impact overall clinical outcome. Co-testing at 12 months following treatment of CIN2/3 without colposcopy is safe and routine colposcopy at collection of the co-test can be omitted.

Identifiants

pubmed: 32935336
doi: 10.1111/ajo.13248
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

959-964

Informations de copyright

© 2020 The Royal Australian and New Zealand College of Obstetricians and Gynaecologists.

Références

Soutter WP, Sasieni P, Panoskaltsis T. Long-term risk of invasive cervical cancer after treatment of squamous cervical intraepithelial neoplasia. Int J Cancer 2006; 118(8): 2048-2055.
Cancer Council Australia Cervical Cancer Screening Guidelines Working Party. National Cervical Screening Program: Guidelines for the Management of Screen-detected Abnormalities, Screening in SPECIFIC Populations and Investigation of Abnormal Vaginal Bleeding. Sydney: Cancer Council Australia, 2016.
Kocken M, Helmerhorst TJM, Berkhof J et al. Risk of recurrent high-grade cervical intraepithelial neoplasia after successful treatment: a long-term multi-cohort study. Lancet Oncol 2011; 12(5): 441-450.
Uijterwaal MH, Kocken M, Berkhof J et al. Posttreatment assessment of women at risk of developing high-grade cervical disease: proposal for new guidelines based on data from the Netherlands. J Low Genit Tract Dis 2014; 18(4): 338-343.
Katki HA, Schiffman M, Castle PE et al. Five-year risks of CIN 3+ and cervical cancer among women with HPV-positive and HPV-negative high-grade Pap results. J Low Genit Tract Dis 2013; 17(5 Suppl 1): S50-S55.
Australian Institute of Health and Welfare. Report on monitoring activities of the National Cervical Screening Program Safety Monitoring Committee [Internet]. Canberra: AIHW, 2013. (Cancer Series 80). Available from: http://www.aihw.gov.au/publication-detail/?id=60129545158).
Thompson V, Marin R. Is colposcopy necessary at twelve months after large loop excision of the transformation zone? A clinical audit. Aust N Z J Obstet Gynaecol 2013; 53(6): 571-573.
Eijsink JJH, de Bock GH, Kuiper JL et al. Routine follow-up intervals in patients with high-grade squamous intraepithelial lesions (HSIL) and free excision margins can safely be increased in the first two years after Large Loop Excision of the Transformation Zone (LLETZ). Gynecol Oncol 2009; 113: 348-351.
Lubrano A, Medina N, Benito V et al. Follow-up after LLETZ: a study of 682 cases of CIN 2-CIN 3 in a single institution. Eur J Obstet Gynecol Reprod Biol 2012; 161: 71-74.
Zhu M, He Y, Baak JP et al. Factors that influence persistence or recurrence of high-grade squamous intraepithelial lesion with positive margins after the loop electrosurgical excision procedure: a retrospective study. BMC Cancer 2015; 15: 744.
Pirtea L, Grigoraş D, Matusz P et al. Age and HPV type as risk factors for HPV persistence after loop excision in patients with high grade cervical lesions: an observational study. BMC Surg 2016; 16: 70.
Arbyn M, Redman CWE, Verdoodt F et al. Incomplete excision of cervical precancer as a predictor of treatment failure: a systematic review and meta-analysis. Lancet Oncol 2017; 18(12): 1665-1679.
Flannelly G, Bolger B, Fawzi H et al. Follow up after LLETZ: could schedules be modified according to risk of recurrence? BJOG Int J Obstet Gynaecol 2001; 108(10): 1025-1030.
Palmer JE, Ravenscroft S, Ellis K et al. Does LLETZ excision margin status predict residual disease in women who have undergone post-treatment cervical cytology and high-risk human papillomavirus testing? Cytopathology 2016; 27(3): 210-217.
Cohen PA. Questioning the value of margin status in treated cervical precancer. Lancet Oncol 2017; 18(12): 1565-1566.

Auteurs

Rhett Morton (R)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Gaithri Mylvaganam (G)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Lyndal Anderson (L)

Department of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

Rhonda Farrell (R)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Jonathan Carter (J)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Selvan Pather (S)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Samir Saidi (S)

Gynaecological Oncology, Chris O'Brien Lifehouse, Sydney, New South Wales, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH