INTRODUCTION
Cervical cancer is a global public health problem caused by persistent human papillomavirus (HPV) infection leading to malignancy [Reference Walboomers1]. For women, it ranks second in terms of cancer incidence and mortality worldwide, and it ranks first in several developing countries. The global burden estimates suggest that annual incidence is 510 000 and mortality is 288 000 each year worldwide.
In France, cervical cancer is ranked number 8 in terms of cancer incidence [Reference Hantz, Alain and Denis2]. In the French overseas territories in the Americas the incidence rates are situated between what is observed in mainland France and the Caribbean [3], one of the most affected regions worldwide [Reference Eluf-Neto and Nascimento4]. In French Guiana, cervical cancer is the second most frequent cancer in females [Reference Roue5], still causing significant mortality [Reference Douine6]. In 2002–2005, the standardized incidence of cervical cancer was 30·3/100 000 women, which was close to that of neighbouring Brazil [Reference Arrossi, Sankaranarayanan and Parkin7]. French Guiana is a sparsely populated region covered by primary forest, with populations living in remote parts of the territory only accessible by boat. Despite a network of health centres connected to the main hospital, there are some difficulties in accessing care. It was recently shown that despite the absence of a significant difference in incidence between rural areas and urban areas, there were some differences in the diagnostic delays with 77% of the women from the rural areas with lesions metastasizing beyond the cervix vs. 44% for women living in urban areas [Reference Roue5]. Health professionals concur that given the early start of sex life in populations living in these remote parts [Reference van Melle8], the risk of cervical lesions due to HPV should be high. In these remote areas, sexual transmission has also driven the HIV epidemic, which has soared from zero to over 1% within a decade [Reference Nacher9]. Given that HPV16–18 are involved in 73% of cervical cancers in Europe, vaccination against these genotypes is now recommended in France. However, little is known about the epidemiology of HPV in French Guiana, a French territory with very different populations and a very different pathogen environment from that of mainland France. The relative isolation of Amerindian and Maroon populations may thus lead to singular epidemiological features. The objective of the present study was thus to describe the prevalence of HPV infections in general, the prevalence of the different genotypes and of cytological anomalies in women aged 20–65 years living in the remote areas of French Guiana.
METHODS
Study population
The source population was women living in the remote villages on the Maroni and Oyapock rivers. The target population was women aged 20–65 years having previously had sexual activity. Enrolment in the study took place between December 2012 and September 2014.
Inclusion criteria. All women from the target population.
Exclusion criteria. Women with a history of hysterectomy, pregnant women (>3 months pregnant).
Data collection. At the time of enrolment a short questionnaire was completed to collect socioeconomic and demographic data, gynecological and obstetrical history.
Study conduct
Before starting enrolment, communication missions were undertaken in all villages in order to sensitize the local populations on this public health problem. Traditional authorities and health centre workers were also informed. Local radio messages informed the population of the dates of the study team's presence in the village. Women wishing to be screened came to the health centre where the project was explained to them. When individuals agreed to participate in the study, a questionnaire was completed and samples were taken and kept in a cooler until the end of the mission. The samples were then sent to the Virology laboratory of Fort de France Hospital, Martinique, where extraction and genotyping were performed using an automated method in order to reduce the risk of error and contamination. DNA extraction was performed using a minimum of 2 ml of the sample in liquid phase.
HPV infection was defined by the detection of HPV DNA using the Greiner Bio-One kit. This kit allows the identification of potentially oncogenic HPV genotypes: 16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 70, 73, 82 and of low-risk HPV genotypes: 6, 11, 40, 42, 43, 44, 55. This kit allowed the identification of multiple infections. Cytological anomalies were described using the 2001 Bethesda classification.
All results were sent to attending physicians for medical care. When HPV was positive and cytology was negative, a gynaecological follow-up was recommended 1 year later with a cervical smear and an HPV test to verify if HPV positivity had disappeared or if cytological lesions were present. If both HPV and cytology were positive, colposcopy was proposed.
Ethical and regulatory aspects
Although it has been shown that HPV tests are superior to cytology for the detection of cervical cancer, in France the HPV test is only reimbursed when the patient has a cytological examination revealing atypical cells of undetermined significance (ASCUS). Here, all patients received the HPV test and cytology free of charge. All participants supplied written informed consent. Regulatory and ethical approvals were given by the Comité d'Evaluation Ethique de l'Inserm (CEEI), approval no. 12-064; the Comité Consultatif sur le Traitement de l'Information en matière de Recherche dans le domaine de la Santé (CCTIRS), no. 12·310; the Commission Nationale de l'Informatique et des Libertés (CNIL), no. 912 459; and the Comité de Recherche Clinique (CoRC) Pasteur Institute, no. 2012-15. The study was funded by the European Regional Development Fund (FEDER presage no. 30814).
Data analysis
Prevalence was obtained by dividing the number of women infected by at least one HPV genotype (high grade or low grade) by the total number of women included. For specific genotypes, prevalence was obtained by dividing the number of women infected by that specific genotype by the total number of women included in the study. Prevalence of cytological anomalies was obtained by dividing the number of women with at least one cytological anomaly by the total number of women with an interpretable cytological examination.
The standardized HPV prevalence rate used the direct standardization method with the world population as a reference.
Unconditional multiple logistic regression was used to predict the variables associated with having a positive HPV test. Different age group-specific models were performed. Categorical variables were transformed into indicator variables. The data were analysed using Stata v. 13 (StataCorp., USA). Mapping was performed using Mapinfo v. 12.0 (USA).
RESULTS
Overall, the population of women living in the remote villages was estimated at 5712 on the Maroni river and 1209 on the Oyapock river. A total of 643 women (406 on the Maroni river, 237 on the Oyapock river) were included and 51 were excluded due to exclusion criteria. On the Maroni river 117 were included in Apatou, 69 in Grand Santi, 86 in Papaïchton, 65 in Maripasoula, 32 in Taluen, and 37 in Antecume Pata. On the Oyapock river 98 were included in Saint Georges, 60 in Camopi, and 79 in Trois Sauts. The ratio between the number of women included in each village and the estimated target population number in each village ranged between a minimum of 6% in Grand Santi to 41·7% in Camopi. Overall, 9·3% of women from the target population entered the study. Overall, sexual relations started at a young age with 27% of the surveyed women had their first sexual relations before age 15, and 50% before age 16.
Table 1 shows very high HPV prevalence notably for high-risk viruses. The overall age-standardized prevalence rate was 35%. There was a U-shaped evolution of overall HPV prevalence by age and high-risk HPV prevalence by age, with women aged >50 years at highest risk for HPV, followed by those aged 20–29 years. Maroon language was associated with a greater HPV prevalence whereas Portuguese language was associated with a lower prevalence. Other risk factors such as number of sex partners, parity, age at first sex, education, contraception, or smoking were not significantly linked to differences in HPV prevalence. None of the women had declared receiving the HPV vaccine.
Figure 1 shows the geographical differences in HPV prevalence with the lower part of the Maroni river having the highest prevalence. Table 2 shows that HPV52 was the most frequent high-risk virus. HPV16 was the second most frequent genotype in women aged <40 years, although it appeared less frequent in women aged >40 years. Overall, the prevalence of HPV16 or 18 exceeded 5% of tested women.
Overall, 139 women had single HPV infections, 53 had double infections, and 22 had ⩾3 different HPV genotypes.
A very large proportion (N = 147, 27·2%) of women with normal cytology had a positive HPV test.
Tables 3 and 4 show multiple regression models predicting HPV positivity for different covariates. Few variables predicted HPV positivity. In the global models women aged 20–29 years and women aged 50–64 years were at higher risk of having a positive HPV test, and of having a high-risk genotype than other age groups, as shown in Figure 1. Table 4 shows that education was independently associated with HPV positivity in women aged 20–29 years but that in women aged 30–39 years, intermediate or high education were independently associated with a lower risk of having a positive HPV test. A reported number of sex partners ⩾2 in the past year was associated with an increased risk of having a positive HPV test in women aged 30–39 years.
DISCUSSION
The overall prevalence of HPV infection in the remote areas of this French territory was much higher than in mainland France. Moreover, the standardized HPV prevalence rate was comparable to, and even higher than in published studies around the world [Reference Franceschi10]. The observed level of prevalence was comparable to what is usually observed in developing countries. High HPV prevalence levels are consistent with the high incidence of cervical cancer observed in French Guiana, which also resembles more what is observed in developing countries than what is seen in France. The age at first sex was lower than in mainland France, with differences between the Maroon regions and the Amerindian regions.
The HPV prevalence varied according to age, and seemed highest in the Maroon villages. As observed elsewhere, and notably in Latin America and Africa, there was a U-shaped curve of HPV prevalence by age group [Reference Forman11, Reference Lazcano-Ponce12]. The prevalence rate reflects the combination of incidence, new infections, and the duration of infection. The U shape may have reflected new infections in these age groups and/or a slower clearance of viruses in older parous women [Reference Molano13]. As seen in earlier studies, apart from age no other variable was significantly associated with the risk of having a positive HPV test [Reference Molano13, Reference Lazcano-Ponce14].
The study limitations were that participation in the study was voluntary, and that women living far from the health centres may have been less likely to be included in the study. Finally, cytology and histology from cervical biopsies would have been important in order to compare the frequency of the genotypes in all women receiving the HPV test and in women with actual cervical lesions. Nevertheless, this is the first study conducted in this border region.
Despite studies repeatedly showing the superior sensitivity of HPV tests over cytology, HPV tests are not reimbursed by French health insurance as screening tools. They are only reimbursed if cytology shows ASCUS lesions or worse. HPV testing can be performed using self-tests, which is less human resource-intensive and could make it more acceptable for some women [Reference Toliman15]. Given the high prevalence of HPV infection and the high incidence of cervical cancer in French Guiana, emphasis on vaccination and expanded and innovative screening seems potentially important [Reference Lynge16, Reference Sankaranarayanan17]. The exact HPV vaccine coverage in these remote territories is unknown, but it is presumably very low. None of the surveyed women reported having been vaccinated. When looking at the variety of HPV genotypes present in these remote territories of French Guiana, the nonavalent HPV vaccines would seem more appropriate that the bivalent or tetravalent vaccines, which do not cover other circulating high-risk genotypes [Reference Londesborough18]. This nonavalent vaccine has been recommended in France [Reference Riethmuller19] and it would presumably have an even greater added value in French Guiana. Presently, given the large proportion of the population that does not have health insurance in these remote areas, the cost of the vaccine is prohibitive. Given the present results, health authorities should attempt to overcome these economic obstacles to ensure that these populations have access to this vaccine.
Overall, the present results show that over a third of women were infected with HPV, and that over a quarter of women with high-risk HPV infection had normal cytology. The high prevalence of HPV and the U-shaped age-specific prevalence observed in the European outermost region of French Guiana are closer to what is observed in poor tropical countries than in Europe. Given the high incidence of cervical cancer in French Guiana and the relative delay in diagnosis [Reference Douine6, Reference Roué and Nacher20], these results emphasize the potential importance of vaccination, preferably with a nonavalent vaccine. However, in this region where a large portion of the population has no health insurance, this still represents a challenge. Finally, expanded screening using HPV self-tests may be beneficial given the potential for operational simplification in an isolated region where health resources are limited and overstretched [Reference Toliman15, Reference Broberg21, Reference Wright22].
ACKNOWLEDGEMENTS
We thank the health professionals of the Centres Délocalisés de Prévention et de Soins and the Protection Maternelle et Infantile. This project was supported by an European Union Grant (PO FEDER 2007-2013, No. Présage: 30814, Guyane Française.
DECLARATION OF INTEREST
None.