Cervical Cancer Flashcards

1
Q

Describe epidemiology of cervical cancer

A

50% occur in women under 45
80% are squamous cell cancers
20% are adenocarcinoma

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2
Q

What are features of cervical cancer?

A

may be detected during routine cervical cancer screening
abnormal vaginal bleeding: postcoital, intermenstrual or postmenopausal bleeding
vaginal discharge

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3
Q

What are RFs for cervical cancer?

A

HPV serotypes 16,18 and 33
Smoking
HIV
Early first sexual intercourse, many partners
High parity
Low socioeconomic status
Combined OCP

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4
Q

How does HPV cause cervical cancer?

A

HPV 16 & 18 produces the oncogenes E6 and E7 genes respectively
E6 inhibits the p53 tumour suppressor gene
E7 inhibits RB suppressor gene

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5
Q

How does cervical screening work?

A

HPV first system - sample is tested for high-risk strains of human papillomavirus (hrHPV) first and cytological examination is only performed if this is positive

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6
Q

Who is screened for cervical cancer and how often?

A

25-49 years: 3-yearly screening
50-64 years: 5-yearly screening
cervical screening cannot be offered to women over 64 (unlike breast screening, where patients can self-refer once past screening age)
in Scotland, it is offered from 25-64 every 5 years

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7
Q

What are special cases in terms of cervical cancer screening?

A

cervical screening in pregnancy is usually delayed until 3 months post-partum unless missed screening or previous abnormal smears.

women who have never been sexually active have a very low risk of developing cervical cancer therefore they may wish to opt out of screening

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8
Q

When in the menstrual cycle is cervical screening performed?

A

Mid-cycle

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9
Q

How is a negative hrHPV interpreted?

A

return to normal recall, unless
the test of cure (TOC) pathway: individuals who have been treated for CIN1, CIN2, or CIN3 should be invited 6 months after treatment for a test of cure repeat cervical sample in the community
the untreated CIN1 pathway
follow-up for incompletely excised cervical glandular intraepithelial neoplasia (CGIN) / stratified mucin producing intraepithelial lesion (SMILE) or cervical cancer
follow-up for borderline changes in endocervical cells

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10
Q

How is a positive hrHPV interpreted?

A

Cells examined cytologically and if samples are abnormal, colposcopy recommended.

Examples of abnormal cytology are:
borderline changes in squamous or endocervical cells.
low-grade dyskaryosis.
high-grade dyskaryosis (moderate).
high-grade dyskaryosis (severe).
invasive squamous cell carcinoma.
glandular neoplasia

If cells are normal, test repeated at 12 months

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11
Q

How are repeat test results interpreted?

A

if the repeat test is now hrHPV -ve → return to normal recall
if the repeat test is still hrHPV +ve and cytology still normal → further repeat test 12 months later:
If hrHPV -ve at 24 months → return to normal recall
if hrHPV +ve at 24 months → colposcopy

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12
Q

What is done if the sample is inadequate?

A

repeat the sample in 3 months
if two consecutive inadequate samples then → colposcopy

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13
Q

How is CIN treated?

A

Large loop excision of transformation zone (LLETZ) is the most common treatment for cervical intraepithelial neoplasia. LLETZ may sometimes be done during the initial colposcopy visit or at a later date depending on the individual clinic.

Alternative techniques include cryotherapy.

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14
Q

What is cervical cancer management determined by?

A

FIGO staging

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15
Q

What are FIGO stages?

A

IA: Confined to cervix, only visible by microscopy and less than 7 mm wide:
A1 = < 3 mm deep
A2 = 3-5 mm deep

IB: Confined to cervix, clinically visible or larger than 7 mm wide:
B1 = < 4 cm diameter
B2 = > 4 cm diameter

II: Extension of tumour beyond cervix but not to the pelvic wall
A = upper two thirds of vagina
B = parametrial involvement

III: Extension of tumour beyond the cervix and to the pelvic wall
A = lower third of vagina
B = pelvic side wall
Any tumour causing hydronephrosis or non-functioning kidney is considered stage 3

IV: Extension of tumour beyond the pelvis or involvement of bladder or rectum
A = involvement of bladder or rectum
B = involvement of distant sites outside the pelvis

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16
Q

How is a stage IA tumour managed?

A

Gold standard: hysterectomy +/- lymph node clearance

For A2, node clearance.
People wishing to retain fertility can opt for a cone biopsy with negative margins
Close follow-up advised
Radical trachelectomy is also an option for A2.

17
Q

How is stage IB tumour managed?

A

B1 tumours: radiotherapy with concurrent chemotherapy
B2 tumours: radical hysterectomy with pelvic lymph node dissection

Radiotherapy may either be bachytherapy or external beam radiotherapy
Cisplatin is the commonly used chemotherapeutic agent

18
Q

How are stage II and III tumours managed?

A

Radiation with concurrent chemotherapy
f hydronephrosis, nephrostomy should be considered

19
Q

How are stage IV tumours managed?

A

Radiation and/or chemotherapy is the treatment of choice
Palliative chemotherapy may be best option for stage IVB

20
Q

How is recurrent disease managed?

A

Primary surgical treatment: offer chemoradiation or radiotherapy
Primary radiation treatment: offer surgical therapy

21
Q

What are complications of surgical treatment?

A

Standard complications (e.g. bleeding, damage to local structures, infection, anaesthetic risk)

Cone biopsies and radical trachelectomy may increase risk of preterm birth in future pregnancies

Radical hysterectomy may result in a ureteral fistula

22
Q

What are the short and long term consequences of radiotherapy?

A

Short-term: diarrhoea, vaginal bleeding, radiation burns, pain on micturition, tiredness/weakness

Long-term: ovarian failure, fibrosis of bowel/skin/bladder/vagina, lymphoedema