Cervical cancer screening, HPV vaccination and testing Flashcards

1
Q

HPV - overview

A
  1. Types 16 and 18 account for 60-80% of all cervical cancer
  2. Infection with high-risk or oncogenic HPV (hrHPV) is necessary for cervical cancer development (virtually all cervical cancers test positive for HPV DNA)
  3. Natural hx: majority of low-grade lesions (LGSIL) regress without tx, whilst most high-grade lesions (HGSIL) progress to invasive cancer if left untreated. Typically takes 7-10y to develop invasive cervical cancer from CIN III
  4. Very common in sexually active males and females
  5. Acute infection -> clinically evident or subclinical infection -> clinically evident disease = warts, CIN
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2
Q

HPV - vaccines

A

Use virus-like particles (but no viral DNA)

  1. Gardasil (quadrivalent) = HPV 16, 18 for cervical cancer, and HPV 6 and 11 for genital lesions
  2. Cervarix (bivalent) = HPV 16, 18
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3
Q

HPV - testing

A

Using a commercial RNA probe-ELISA kit

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4
Q

Pap smears - screening program

A
  1. Women 18-70y who have ever had sexual intercourse
  2. Every 2y

Special circumstances

  1. Pregnancy - should not cause deviation unless known low-lying placenta
  2. Immunosuppression - annual Pap tests, colposcopy if detected abnormality
  3. If subtotal hysterectomy (i.e. cervix retained), continue with routine screening. If total hysterectomy, no further screening required
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5
Q

CIN/new terminology

A
LGSIL = CIN I
HGSIL = CIN 2 or 3
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6
Q

CIN - overview

A
  1. Necessary precursor lesion for development of cervical carcinoma. Histological dx = loss of differentiation and maturation from the basal layer of the squamous epithelium upwards
  2. Needs persistent cervical infection with HPV to develop (high risk 16, 18, 31 and 45)
  3. CIN 1 = mildly atypical cellular changes in the lower third of the epithelium
  4. CIN 2 = moderately atypical cellular changes confined to basal 2/3 of epithelium
  5. CIN 3 = severely atypical cellular changes encompassing >2/3 of eptihelial thickness, and includes full thickness lesions (formerly called severe dysplasia or carcinoma in situ)
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7
Q

CIN - risk factors

A
  1. Exposure to HPV - early first sexual experience, multiple partners, non-barrier contraceptive
  2. COCP
  3. High parity
  4. Smoking
  5. Immunosuppression
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8
Q

Colposcopy

A
  1. Examination of cervix and lower genital tract with low power, stereoscopic microscope with attached light source
  2. Cervix and vagina cleaned of any blood and debris with NS
  3. Cervix inspected and 3-5% acetic acid applied; causes acetowhite epithelial changes in dysplastic cells
  4. Lugol’s iodine may be applied - taken up by normal cells; dysplastic cells iodine negative
  5. Directed punch biopsy to gain histological confirmation
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9
Q

LGSIL - management algorithm

A
  1. Repeat in 12 mo
    a. If low-grade again, colposcopy
    - If high-grade disease excluded on colposcopy, repeat Pap in 6mo
    - If high-grade disease, tx
    b. If normal, back to Pap in 24mo
  2. If over 30 and no recent Pap, repeat Pap in 6mo or colposcopy
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10
Q

HGSIL - mx algorithm

A
  1. Colposcopy and biopsy
    a. If high-grade disease confirmed, treat
    b. If high-grade disease not confirmed, review in 3-6mo
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11
Q

HGSIL - tx

A
  1. LEEP (loop electrocautery excision), or LLETZ (large loop excision of transformation zone)
  2. Laser surgery using invisible CO2 laser beam
  3. Cold knife cone biopsy for adenocarcinoma in situ only
  4. Electrocoagulation diathermy (ECD)
  5. Cryosurgery with N2O or CO2 (under-resourced countries)
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12
Q

LLETZ - complications

A

Short-term
1. Haemorrhage
2. Infection
3. Vasovagal reaction
Long-term
4. Cervical stenosis (dysmenorrhoea and/or difficulty in follow-up)
5. Cervical incompetence and premature delivery (but evidence suggests absolute risk of adverse effect on neonatal outcome is very low)

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13
Q

Follow up after tx of HGSIL (3)

A
  1. Review 4-6mo after treatment for Pap smear +/- colposcopy
  2. Review 12mo after treatment for Pap smear, colposcopy and HPV DNA testing
  3. Once two sets of tests are negative on two consecutive 12-monthly occasions, the woman may return to the usual 2-yearly screening interval (i.e. after 36mo after tx and all negative tests). If Pap test or HPV not negative, continue with yearly review
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