cervical screening update louise cadman research nurse consultant and nurse colposcopist centre for...
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CERVICAL SCREENING UPDATE
Louise Cadman
Research Nurse Consultant and Nurse Colposcopist
Centre for Cancer Prevention
Wolfson Institute of Preventive Medicine
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E-LfH Learning Portal – (e-SRH) Sexual and Reproductive Healthcare – Cervical Screening
Learning objectives:State the objectives of the cervical screening programme Identify the principles of screening programmes Explain the way screening programmes operate in the UK Identify the causes and prevalence of cervical screening abnormalities Manage cervical screening results correctly Explain colposcopy to a patient
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Cervical cancer – the size of the problem
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Worldwide cervical cancer incidence 2012
• fourth most common cancer worldwide for females
• seventh most common cancer overall
• >527,000 new cases diagnosed
• 266,000 deaths
• 85% in the developing world
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The 20 most common cancers in women, 2011Number of New Cases, UK
12th most common cancer amongst females in the UK
2851 cases/year 972 deaths/year 67% survived ≥ five years
(2005-2009)
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Age-specific incidence rates and number of cases diagnosed by five year age group, England 2009
6 in 10 of all new cases of cervical cancer are diagnosed in women under 50 years
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European Age-Standardised Cervical Cancer Incidence & Mortality Rates per 100,000 Female Population, UK
Prepared by Cancer Research UKOriginal data sources:Office for National Statistics. Cancer Statistics: Registrations Series MB1. http://www.ons.gov.uk/ons/search/index.html?newquery=series+mb1Welsh Cancer Intelligence and Surveillance Unit. http://www.wcisu.wales.nhs.ukInformation Services Division Scotland. Cancer Information Programme. www.isdscotland.org/cancer
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1975-2011 European age-standardised incidence rates of cervical cancer per 100,000 population, by
age, females, Great Britain
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Number of cases by morphology, England 1988-2009
0
500
1000
1500
2000
2500
3000
1988
1989
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
Year of Diagnosis
Squamous
Adenocarcinoma
Unclassified EpithelialAdenosquamous
Neuroendocrine
Other Epithelial
Other
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Cervical screening as secondary prevention of cervical cancer
Cervical screening → ↓morbidity ↓ mortality
! Limitations:does not prevent:
oncogenic HPV infection precursor lesions (high grade Cervical Intraepithelial Neoplasia (CIN))
less efficient for early stages of adenocarcinomascreening programmes not achievable in many countriesmay not detect lesions which progress quickly in timeonly effective if women attend regularly, when invited
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NHS Cervical Screening Programme Coverage
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Source: KC53, Health and Social Care Information Centre.
Five year coverage of the target age group (25-64), Primary Care Organisation, England, 31st March 2013
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Cervical screening coverage by London Primary Care Organisation, 2012-13
(% less than 5 years since last adequate test)
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NHS Cervical Screening Programme, 2003-2013: coverage-less than 5 years (%)
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Five year coverage of the target age group (25-64) England at 31st March, 2003 to 2013
© Data prior to 2005, re-used with the permission of the Department of Health.Source: KC53, Health and Social Care Information Centre.
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Anatomy of the cervix
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The Uterine Cervix Uterus ÷
Upper body Cervix
Cervix Cylindrical ~ 3cm length ~ 2.5cm diameter 1/3 protrudes into the
vaginal vault Os – the hole Ectocervical = outside the
external os Endocervical = inside
cervical canal
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Stratified squamous epithelium
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Columnar epithelium
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Squamo-columnar junction (SCJ)
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Cervical Epithelium
Squamous epithelium Usually on ectocervix Cells are multilayered Usually appears as smooth,
shiny, pale pink Columnar epithelium
Mostly endocervical Single layer column shaped cells Delicate and usually appears red
(ectopy when on ectocervix) Squamo-columnar junction
(SCJ)
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Transformation zone
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HPV Infection in the Cervix
Normal Epithelium
HPV Infection CIN I CIN II CIN IIICancer
DecadesYearsMonths
HPV infects cell integrates its DNA into the host cell DNA
Persistence cell damage (pre-cancer)
Eventually cancer
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Dyskaryosis – identified by cytology
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CIN 1
CIN 3
CIN 2
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Screening intervals and sample taking
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Screening Intervals in England
25 years - first invitation from GP lists
invitation should not be before age 24.5 years
25–49 years - three yearly
50–64 years - five yearly
65+ years - only screen those not screened since age 50 or with recent abnormal tests
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Summary percentage preventable by 3- and 5-yearly screening
Annual 3 yearly 5 yearly
20–39 years
76% 61% 30% (39%)
40–54 years88% 84% 73%
55–69 years87% 87% 83%
* The percentage in parentheses is obtained by replacing RRs greater than one with 1.0 when averaging
Benefit of cervical screening at different ages: evidence from the UK audit of screening historiesP Sasieni, J Adams and J Cuzick
British Journal of Cancer (2003) 89, 88–93.
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Samples examined by source of sample, 2012-13
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31
Prior to the examination
Some women may wish to agree a non-verbal
sign
Some women prefer it if you ‘just get on with it’
Avoid the word relax!
Be realistic in the length of time it should take
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Taking a sample
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Following the examination
Explain that spotting
following the test is possible
and to be expected
If you cannot visualise the cervix, and nor can any
colleague you ask to assist, then the procedure should be abandoned and
referral made to a colposcopy clinic
From: Cervical screening - RCN guidance for good practice
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Results and referral to colposcopy
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Results of adequate tests for women aged 25-64, 2012-13
Total number of results: 3,283,438
• 99.8% of reports authorised within 0-2 weeks (0-14 days)• 0.2% of reports authorised within 3-4 weeks (15-28 days)
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Cytology results by region and Primary Care Trust, 2012-13
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Cytological referral for colposcopy or further assessment
Suggestion of invasive carcinoma (x1) Suggestion of glandular lesion (x1) Severe dyskaryosis (x1) Moderate dyskaryosis (x1) Mild/borderline and hr HPV +ve (x1) Persistent unsatisfactory smears (x3) 3 abnormal tests, any grade, in 10 year
period Treated for CIN, have not been returned to
routine recall and a subsequent test is reported as mild dyskaryosis or worse
URGENT - to be seen within 2 weeks
URGENT - to be seen within 4 weeks
ROUTINE - to be seen within 8 weeks
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Cytology terminology and result codes
Previous terminology(BSCC 1986)
New Terminology
Result code
Borderline changes Borderline changes in squamous cells (not HPV Tested) 8
Borderline changes in squamous cells (HPV tested) B
Borderline changes in endocervical cells (not HPV Tested) 9
Borderline changes in endocervical cells (HPV tested) E
Mild dyskaryosisBorderline changeswith koilocytosis
Low-grade dyskaryosis (not HPV Tested) 3
Low-grade dyskaryosis (HPV tested) M
Moderate dyskaroysis High-grade dyskaryosis (moderate) 7Severe dyskaroysis High-grade dyskaryosis (severe) 4Severe dyskaryosis?Invasive
High-grade dyskaryosis ?Invasive squamous carcinoma 5
?Glandular neoplasia ?Glandular Neoplasia endocervical type 6?Glandular Neoplasia (non-cervical) (not HPV Tested) 0
?Glandular Neoplasia (non-cervical) (HPV tested) G
Negative Negative (Not HPV tested) 2 Negative (HPV tested) NInadequate Inadequate 1
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Clinically suspicious cervix Post-menopausal bleeding
Not using HRT
Symptoms → gynaecologist → colposcopy Post-coital bleeding
(particularly in women > 40 years of age) Intermenstrual bleeding Persistent vaginal discharge
Previous treatment for CIN Not returned to routine recall Test result > mild dyskaryosis
Referral for colposcopy or further assessment
URGENT - to be seen within 2 weeks
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Direct referral for colposcopy
Colposcopy Programme and Management Guidelines (2010) state that:At least 90% of women with an abnormal test should be seen in a colposcopy clinic within 8
weeks of referral and that at least 90% of women with a test result of moderate or severe dyskaryosis should be seen within 4 weeks
Sample taken
Sample processed and cytology results
available
Sample taker receives results and made aware of direct referral
Direct referral from laboratory to colposcopy
Sample taken
Sample processed and cytology results
available
Sample taker receives results and refers to colposcopy
Referral from GP to colposcopy.
Patient sent appointment
Smear taker referral for colposcopy
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COLPOSCOPY
Louise Cadman
Research Nurse Consultant and Nurse Colposcopist
Centre for Cancer Prevention
Wolfson Institute of Preventative Medicine
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To determine extent of the lesion Visualise the entire squamocolumnar or the colposcopy is
‘unsatisfactory’. Identify the transformation zone (TZ).
Obtain directed biopsies from abnormal/-suspicious areas
To confirm nature of lesion and to rule out invasion
Aims of Colposcopy
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Colposcopy
A specialist technique Gives a magnified image of the cervix Solutions applied which reveal changes in the epithelium
5% acetic acid Iodine
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Colposcopic signs
VESSELS
COLOURMARGINS
IODINE
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Normal Colposcopy
with acetic acid
with iodine
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CIN I
with acetic acid
with iodine
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2012-3 Procedure at colposcopy by reason for referral (N=3,320,389)
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Treatment Methods
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Large Loop Excision of the Transformation Zone - LLETZ
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Large Loop Excision of the Transformation Zone - LLETZ
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LLETZ
Local anaesthetic Cuts blocks up to 1.5 cm
deep Provides a specimen for
histology Good haemostasis Quick and simple Little thermal damage to
cervix or specimen
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Cold coagulation
Heats superficial tissues to 100°C
Suitable for small lesions / low grade CIN
Rapid (20 seconds per field)
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Cryocautery
Freezes using nitrous oxide
Treatment ablates affected area
Treats to a depth of 4 mm
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LASER
Light
Amplification
Stimulated
Emission of
Radiation
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Cold knife cone biopsy
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Future developments
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Prophylactic Vaccines
Gardasil(Sanofi Pasteur MSD)
Quadrivalent HPV types 6,11,16
and 18 Adjuvant –
aluminium salts
Cervarix(GSK)
Bivalent HPV types 16 and
18 Adjuvant – ASO4
UK vaccination programme introduced in September 2008
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Previous calculation: number of cancers could be reduced to 1000
6000 cytology screening samples + pathology samples HPV 16 and 18 found in
76.4% of squamous cell cancers 81.9% of adenocarcinomas 63% of CIN 3 91% of high grade glandular lesions
Frequently found multiple HPV types in a lesion Number of cancers could be reduced to 700
Recent results for HPV prevalence in England
Howell-Jones R, et al Br J Cancer 2010:103;209-16; doi:10.1038/sj.bjc.6605747
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Monitoring after vaccination
Monitoring essential: type-specific HPV tests needed
Duration of protection 15 - 30 years?
booster needed?
Relevance of antibody levels
Detection of non-vaccine HPV types
Cuzick J, et al. Vaccine 2008; 26S:K29–K41 Fraser C, et al. Vaccine. 2007; 25:4324–4333
David MP, et al. Gynecol Oncol. 2009
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Screening in the era of vaccination:challenges and possibilities
HPV as primary screen?
Increase screening interval to ?5 years
Transience of infection At what age to start?
Maybe age 30? Triage using cytology?
When to refer for colposcopy?
Median duration time of HPV infection (months)
Any 9.8
hrHPV 9.3
lrHPV 8.4
16 12.4
18 9.8
Swab Tampon Vaginal
washings Brush
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New developments
Nonavalent human papillomavirus (HPV) vaccine, including HPV-types 6/11/16/18/31/33/45/52/58
Therapeutic vaccine: ProCervix - bivalent HPV 16 and 18
therapeutic vaccine
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Useful websites64
www.jostrust.org.ukwww.bsccp.org.uk
www.cancerscreening.nhs.uk