Cervical cancer screening by visual inspection in Côte d'Ivoire, operational and clinical aspects according to HIV status

Study population

Our study was a one-shot cervical cancer screening procedure based on visual inspection methods implemented in a sample of HIV care clinics providing ART in Abidjan and involved in "the International epidemiological Database to Evaluate AIDS (IeDEA) in West Africa" http://mereva.net/iedea [17]. Due to logistic and financial constraints, only three of the six adult HIV clinics involved in the IeDEA collaboration were invited to participate. Two nongovernmental organizations, the ACONDA-CePReF (Yopougon) and the ACONDA-MTCT plus (Abobo) together with the national center for blood transfusion (CNTS) (Treichville) were selected in order to cover all the three districts where the IeDEA West Africa sites are already implemented in Abidjan. The CNTS was also selected for its capacity to recruit HIV-negative women. From August 2009 to November 2010, a mobile team composed of three certified midwives and a senior gynaecologist was in charge of proposing cervical cancer screening to all HIV-positive women attending these three clinics for their routine HIV follow-up. The clinics were sequentially involved for a period of six (CePReF, Yopougon), four (MTCT plus, Abobo) and seven (CNTS, Treichville) months, according to the number of women usually attending these services. From May to November 2010, a referent group of HIV-negative women who attended the CNTS clinic for blood donation were also proposed this same cervical cancer screening procedure. Identical exclusion criteria (i.e. history of cervical cancer or total hysterectomy, aged < 25 or > 65 years, pregnancy > 20 weeks) were applied to both HIV-negative and HIV-positive women. Midwives and doctors were not blinded to HIV status.

Screening procedure

After obtaining written informed consent from the women and collecting participant's history, midwives conducted a gynaecological examination. An unlubricated bivalve speculum was inserted into the vagina by the midwife who examined the cervix using a halogen focus lamp and identified the squamocolumnar junction (SCJ). After cleaning away any excess mucus using a cotton swab, a five percent acetic acid solution was applied to the cervix for visual inspection with acetic acid (VIA). Findings were visible one minute after application. A positive VIA was characterised by a well-defined, dense acetowhite area with regular or irregular margins, close to or abutting the SCJ in the transformation zone or when the whole cervix or a cervical growth turned acetowhite. Following VIA, visual inspection with Lugol's iodine (VILI) was also performed. A positive VILI test was characterised by a dense, thick, bright, mustard-yellow or saffron-yellow iodine non-uptake area seen in the transformation zone, close to or abutting the SCJ or when the entire cervix or a cervical growth turns densely yellow. Results of VIA and VILI were both classified as negative, positive or indicative only of ICC according to the International Agency for Research on Cancer (IARC) training manual and recorded on the study questionnaire following each test [18]. The use of both VIA and VILI for cervical cancer screening relies on previous reports that showed an improvement in diagnostic performance by combining the two methods [19]. Midwives mapped positive lesions with both VIA and VILI on the clinical form and assessed the following items: number of positive lesions, number of quadrants of the cervix involved and if the lesion(s) extend to the endocervical canal. Positively screened women as well as women with inconclusive examination were systematically referred for a colposcopic examination. Women with a negative examination but presenting with cervical inflammatory lesions were systematically referred for repeat VIA and VILI tests three weeks after being prescribed appropriate antibiotics. Prior to the study conduct, midwives were trained to perform and report VIA and VILI during a four-day intensive course. Additional training included discussion and review of pictures of normal and abnormal cervix as well as practice in volunteer subjects. Refresher courses were given during the study period. The colposcopic consultation was carried out in the same clinics where the women were initially screened, on a weekly basis, by a senior gynaecologist. Referred women were assessed with colposcopy and directed biopsies were performed if needed and sent to the Abidjan university hospital pathology unit of Abidjan. Histopathological findings were categorized into five classes: normal or non-neoplasic changes, cervical intraepithelial neoplasia grade 1 (CIN1) including HPV changes, CIN2, CIN3 and ICC as described elsewhere [13]. Women with positive or inconclusive VI were systematically addressed on the same week or a week after to a medical consultation. If not showing up to this first visit, women were contacted by phone calls to schedule another visit. After a maximum of three attempts (one per week), women who did not show-up or who could not be contacted were considered as loss to follow-up (LTFU) and called back once to state their reason for not attending. To enhance participation to the cervical cancer screening in our targeted population and obviate LTFU, women were orally counselled about the risk of cervical cancer and the potential benefits of an early detection. Group counselling was provided by midwives on a daily basis in the waiting rooms of the HIV clinics or the CNTS. Leaflets to sensitize women to cervical cancer and its prevention were also distributed during these sessions. Patients with CIN or cancer were offered appropriate follow-up and treatment according to local recommendations. The entire screening procedure was free of charge as well as the ensuing treatment in case of positive findings. This study was approved by the national ethics committee for HIV research in Côte d'Ivoire.

Statistical analysis

Analyses were first conducted to compare the women characteristics according to HIV status using Pearson's χ2 or Fisher's exact test, when appropriate, for qualitative variables, and t-test or Wilcoxon test for quantitative variables. A logistic regression model was used for univariate and multivariate analyses of the association between the main outcome of the cervical screening test (i.e. positive visual inspection, inflammatory lesions of the cervix, unsatisfactory examination) and the HIV status. Proportions and odds ratio (OR) estimates were reported with their 95% confidence intervals (95% CIs). All statistical analyses were performed using SAS software, version 9.1 (SAS Institute Inc, Cary, NC, USA).

General characteristics

The 2,998 HIV-positive women had a median CD4 count of 291 [inter-quartile range (IQR) 156-461] cells/mm³ at enrolment in HIV care and 452 [IQR 301-621] cells/mm³ at last known follow-up visit for HIV infection. The median time between cervical screening and last known CD4 count measure was 4 [IQR 2-6] months. Current ART use was reported in 2,267 (75.6%) HIV-positive women with a median time since ART initiation of 28 months [IQR 12-50].

Cervical screening outcomes

The frequency of positive visual inspection in HIV-positive women was 9.0% (95% CI 8.0-10.0), significantly higher than the 3.9% estimate (95% CI 2.7-5.1) found in HIV-negative women (p < 10^-4). Main results of the cervical screening program according to HIV status are summarized in Figure 1.

Loss to follow- up

Among the 82 women LTFU, 64 were reached by telephone and 55 reported the reason for not attending the physician consultation: 39 (70.9%) did not attend for financial reasons (expected cost related to transport, diagnosis and treatment in case of confirmed cervical lesions), 14 (25.5%) for lack of time (being busy or simply forgot) and two women (3.6%) reported not willing to know more about their cervical cancer status.

Outcomes of cervical screening according to HIV status

A higher rate of precancerous lesions of the cervix or ICC was found in HIV-positive women, consistent with previous reports from sub-Saharan Africa [2]. This finding confirms the need to urgently implement routine cervical cancer screening programs in HIV clinics in West Africa. Regardless of HIV status, the frequency of positive VI and histologically confirmed CIN lesions was relatively low compared to other reports in Africa. In the southern Africa region, a higher frequency of positive VI had been previously reported in HIV-infected women, ranging from 32.6% to 43.7% in South Africa and Zambia, respectively [8, 20]. Recent cervical screening program based on VIA conducted in Mali and Tanzania among 14,141 and 10,378 women regardless of HIV status, reported 1,005 (7.1%) and 274 (2.6%) of histologically confirmed CIN, respectively [21, 22]. In Botswana, a cervical cancer screening programme based on VIA conducted in 2,175 HIV-positive women reported 331 (15.2%) histologically confirmed CIN [23]. Discrepancies in the frequency of positive VI and precancerous lesions according to VI-based studies might be partly related to the limited reproducibility of these screening methods as well as inclusion criteria such as age that differed according to studies. These regional disparities might also be related to other factors such as cultural differences in sexual life (polygamy, number of sexual partners) that have an influence on sexually transmitted viruses such as oncogenic HPV and finally on the burden of cervical malignancies in sub-Saharan Africa. However, our findings are supported by a recent study conducted in Côte d'Ivoire that found similar frequencies of positive VIA in 2,713 HIV-positive (11%) and 743 HIV-negative women (3%) [24]. Although it remains unclear whether the HIV epidemic has impacted the incidence of ICC in sub-Saharan Africa, it is noteworthy that high ICC incidences are reported in countries with the highest prevalence of HIV [25].

Cervical screening programs based on VIA and/or VILI have previously demonstrated to be an adapted alternative to cytology in both HIV-positive and HIV-negative populations from resource-limited settings [13, 14]. To avoid LTFU and tackle human resource shortage for cervical cancer diagnostic and treatment algorithms, a 'see-and-treat' approach proposing an immediate cryotherapy for positively screened cervical lesions with limited extension has been developed and implemented [11, 26, 27]. Usual criteria for postponing an immediate cryotherapy in a 'see-and-treat' strategy are as follows: lesions occupying > 75% of the transformation zone or more than three quadrants of the cervix, lesions extending into the endocervical canal that cannot be completely visualized and lesions too large to fit the largest available cryotherapy probe [27]. Our study was not initially designed to perform a 'see-and-treat' strategy. Thus, we did not formally address the rate of ineligible women referred for a delayed treatment. However, based on clinical reports of midwives who performed the visual inspection, a high frequency of extensive lesions was observed in our study population, especially in HIV-infected women. This might directly impact on their risk of being in need for a delayed treatment. In Zambia, results from a 'see-and-treat' program using VIA in 8,823 women attending HIV care clinics reported that 2,378 (26.9%) were immediately treated with cryotherapy and 1,477 (16.7%) referred for physician evaluation [20]. In Botswana, a 'see-and-treat' program based on VIA in 2,175 HIV-positive women reported that 253 (11.6%) effectively underwent an immediate cryotherapy and 575 (27.3%) were referred for a delayed medical evaluation [23]. Reports from Ghana and India on 'see-and-treat' programs in the general population found a proportion of ineligible women to an immediate cryotherapy of 2.5% and 25.2%, respectively [26, 27]. Thus, the follow-up of ineligible women for an immediate treatment remains a major issue, especially in HIV-positive populations.

Loss to follow-up

The proportion of positively screened women who did not attend the medical consultation prior to the application of a tracking system is consistent with a previous report from Zambia where 40.8% of positively screened women ineligible for an immediate cryotherapy and referred to a physician examination did not show up [20]. The adjunction of a simple tracking procedure based on telephone calls inviting to the mobile medical consultation for colposcopic examination allowed a major reduction in the proportion of women LTFU. However, a significant rate of LTFU remained. A particular effort must be done to sensitise women to the importance of cervical malignancies and the advantages of an early identification of precancerous lesions of the cervix. Finally, the implementation of a 'see-and-treat' approach should be incorporated into cervical screening in our West African network considering the experience reported in Zambia among others. However, even if a single visit approach is used, an important proportion of HIV-positive women presenting with more extensive lesions will not be eligible for this 'see-and-treat' approach. Additional research is needed in order to more efficiently reduce the attrition proportion in cervical cancer screening programs. Studies exploring reasons for being LTFU as well as alternative interventions to minimize it need to be developed.

Limitations

Because only women who were VI positive underwent histological sampling, the performance of VI could not be assessed. Accuracy studies on VI showed contrasting results. While a recent meta-analysis mostly based on observational studies reports a 80% sensitivity (range, 79%-82%) and a 92% specificity (range, 91%-92%) of VIA in detecting high-grade precancerous lesions [28], several randomised trials have shown poorer performance of VIA (sensitivity of 55%) compared to HPV testing (sensitivity 90%) in both HIV-negative and HIV-positive women [9, 29]. As cytology or HPV testing are currently not available, we believe that VI is the most appropriate approach that can at least promote the awareness and initiate the infrastructure for building cervical cancer screening in HIV clinics in Côte d'Ivoire. However, the true performance of VI in this particular context remains to be evaluated. The results reported from this sample of HIV care clinics might not be directly extrapolated to other clinics in West Africa, especially those not located within the proximity of a referral hospital. Nevertheless, the participation of clinics of various sizes and from different health care levels enabled us to extend our findings to at least the HIV care system of Côte d'Ivoire. VI of the cervix remains highly related to the operator skills and subject to misclassification bias. Despite an adapted initial training of midwives associated with refresher courses during the study period, a high and sustained proportion of positively screened women were considered negative after colposcopic examination and did not undergo directed biopsy. The rate of false positivity according to colposcopic results was higher compared to prior accuracy studies conducted by IARC in Africa and India were 2,887 (33%) of the 8,848 women with positive VIA were recused for a directed biopsy [12]. These differences probably reflect the wide range in accuracy parameters (Se, Sp, PPV and NPV) of VI related to the subjective, provider-dependent nature of the test and the underlying frequency of disease. However, when considering a 'see-and-treat' approach based on VI, a significant part of positively screened women might be over-treated with cryotherapy. Although the short-term safety of cryotherapy performed immediately after VI has been relatively well addressed, its long-term safety, especially in HIV-infected women remains to be explored [30]. Alternative screening strategies including more accurate and reproducible tests such as the rapid HPV test will ultimately be needed to enhance the performance of screening for the identification of precancerous lesions.