world cancer report - iarc
world cancer report - iarc
world cancer report - iarc
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Fig. 4.48 Women at a clinic in India participating<br />
in a study of early detection of cervical <strong>cancer</strong>.<br />
the liquid-based method seems to result<br />
in more slides being classified as having<br />
low-grade squamous epithelial lesions or<br />
higher, which were classified as having<br />
less severe disease by conventional<br />
smears, than the reverse situation. The<br />
difference in cost between liquid-based<br />
and conventional cytology is unclear<br />
because of substantial uncertainty about<br />
the relative effectiveness of these two<br />
approaches[13].<br />
It has been suggested that improvements<br />
in the detection of dyskaryosis (abnormal<br />
changes in cell nuclei) using extended tip<br />
plastic spatulas instead of the traditional<br />
wooden Ayre’s spatula would be of<br />
approximately similar magnitude to the<br />
improvements which might result from<br />
replacing conventional cytology with<br />
liquid-based methods [14]. Automated<br />
cytology reading systems are under development<br />
and some health economic evaluation<br />
has been carried out.<br />
In view of the importance of HPV in the<br />
etiology of cervical <strong>cancer</strong>, HPV testing to<br />
allow women to be classified as high-risk<br />
HPV-positive (displaying HPV types associated<br />
with an increased risk of cervical<br />
neoplasia) or negative (otherwise) could<br />
be used as an adjunct to cytological<br />
smear tests. However, the possible value<br />
of HPV testing in the triage of women with<br />
low-grade abnormalities is uncertain.<br />
Alternatives to the Pap smear<br />
HPV testing<br />
HPV testing may be used for primary<br />
screening. In developed countries, most<br />
attention has been focused on HPV testing<br />
as an adjunct to cytological screening<br />
170 Prevention and screening<br />
(see above), in part because of ethical and<br />
medico-legal problems which might ensue<br />
in conducting a randomized trial which<br />
would involve withdrawal of the offer of<br />
cytological screening from the group<br />
assigned to be offered HPV testing. This<br />
would not be the case for populations in<br />
which Pap testing has not been introduced,<br />
notably in developing countries.<br />
The major issues in relation to such use of<br />
HPV testing have been the cost of the test<br />
itself and its relatively poor specificity<br />
[15,16]. Poor specificity results in followup<br />
for women without cervical disease,<br />
incurring costs which may be more than<br />
the society can afford. In both developed<br />
and developing countries, the development<br />
of primary screening based on HPV<br />
tests might be rendered obsolete by mass<br />
HPV vaccination (Human papillomavirus<br />
vaccination, p148).<br />
Visual inspection<br />
Unaided visual inspection of the cervix by<br />
nurses and other non-medical health<br />
workers, also known as “down-staging”,<br />
has been proposed for developing countries<br />
which lack the laboratory facilities or<br />
resources to implement cytological<br />
screening [17]. Women with abnormal<br />
findings require further investigation,<br />
which entails a cytological test if appropriate<br />
facilities are available, or specialist<br />
medical examination if no cytology services<br />
are available.<br />
In view of the unsatisfactory performance<br />
of unaided visual inspection, consideration<br />
has been given to aiding naked-eye<br />
visual inspection by impregnating the<br />
cervix with 3-4% freshly prepared acetic<br />
acid to detect acetowhite areas (Fig.<br />
4.47). This screening approach is known<br />
as visual inspection with acetic acid (VIA)<br />
(synonyms are cervicoscopy and direct<br />
visual inspection). In studies in China,<br />
India, South Africa and Zimbabwe, visual<br />
inspection with acetic acid has emerged<br />
as a satisfactory screening test to detect<br />
cervical <strong>cancer</strong> precursor lesions, with a<br />
sensitivity ranging from 67 to 90% [14,<br />
18-20]. This is similar to (or higher than)<br />
the sensitivity of cytological screening,<br />
but specificity is generally lower (range is<br />
64-92%). Therefore, if screening based on<br />
visual inspection with acetic acid is instituted,<br />
a potential consequence would be<br />
high rates of referral for further investigation.<br />
Currently, randomized intervention<br />
trials are in progress in India to evaluate<br />
the cost-effectiveness of visual inspection<br />
with acetic acid in cervical <strong>cancer</strong> screening<br />
[21].<br />
Addition of magnification to visual inspection<br />
with acetic acid has not further<br />
improved the test performance [14, 22].<br />
Cervicography involves the taking of a<br />
photograph of the acetic acid-impregnated<br />
cervix to be reviewed by trained cervicographic<br />
interpreters. Cervicography<br />
has been found to have a lower sensitivity<br />
than cervical cytology [14, 23], and also<br />
<strong>report</strong>edly suffers from high false positive<br />
rates [24].