- Research article
- Open Access
Evaluation of human-papillomavirus testing and visual inspection for cervical cancer screening in Rwanda
BMC Women's Health volume 18, Article number: 59 (2018)
A pilot screening campaign in Rwanda, based on careHPV-testing followed by visual inspection with acetic acid triage (careHPV+VIA triage), was evaluated against other WHO-recommended screening options, namely HPV screen-and-treat and VIA screen-and-treat.
764 women aged 30-69 underwent at visit 1: i) VIA, and cervical cell collection for ii) careHPV in Rwanda, and iii) liquid-based cytology and GP5+/6+ HR-HPV PCR in The Netherlands. All 177 women positive by VIA, careHPV and/or PCR were recalled, of whom 84% attended. At visit 2, VIA was again used to triage screen-positive women for treatment and to obtain biopsies from all women either from visible lesions or at 12 o’clock of the squamocolumnar junction. Cross-sectional screening indices were estimated primarily against histological high-grade squamous intraepithelial lesions or worse (hHSIL+), after imputation of missing histology data, based on 1-visit or 2-visit approaches.
In a 1-visit screen-and-treat approach, VIA had sensitivity and specificity of 41% and 96%, respectively, versus 71% and 88% for careHPV, and 88% and 86% for PCR. In a 2-visit approach (in which hHSIL+ imputed among women without visit 2 were considered untreated) careHPV sensitivity dropped to 59% due to loss of 13% of hHSIL+. For careHPV+VIA triage, sensitivity dropped further to 35%, as another 24% of hHSIL+ were triaged to no treatment.
CareHPV was not as sensitive as gold-standard PCR, but detected considerably more hHSIL+ than VIA. However, due to careHPV-positive hHSIL+ women being lost to follow-up and/or triaged to no treatment, 2-visit careHPV+VIA triage did not perform better than VIA screen-and-treat.
Cervical cancer is the most commonly occurring female cancer in Rwanda, with a high incidence rate typical of many sub-Saharan African countries (42 cases per 100,000 women per year ). In response to this burden, Rwanda embarked upon a national plan for cervical cancer screening  and, in 2011, was the first African country to initiate a national vaccination program against human papillomavirus (HPV) [2, 3], the necessary cause of cervical cancer .
In order to also reduce cervical cancer among older cohorts of women unprotected by the vaccination program, in 2013, the Rwandan Ministry of Health (MoH) initiated a screening campaign. This campaign was based on primary careHPV testing and the use of visual inspection with acetic acid (VIA) to triage careHPV-positive women for treatment . Indeed, WHO guidelines for cervical screening in low and middle income countries (LMIC) include an algorithm of high-risk (HR) HPV-testing followed by VIA triage as one of its three recommended screen-and-treat options . Although some experiences have since been reported [6,7,8], WHO recommendations acknowledged that there was no evidence on the effectiveness of VIA triage among women known to be HR HPV-positive. The prediction of the efficacy of a HPV + VIA triage approach, as well as its recommendation over a VIA screen-and-treat approach, came from combining evidence of separate performances of HPV and VIA .
We nested an evaluation of the 2013 Rwandan MoH screening campaign within the framework of a population-based HPV survey performed in collaboration between the Rwandan MoH and the International Agency for Research on Cancer (IARC) to jointly monitor the impact of HPV vaccination  and cervical screening. The careHPV-testing followed by VIA triage algorithm was principally evaluated against the gold standard of high-grade squamous intraepithelial lesions or worse (HSIL+) as detected by histology, and was compared with the other two WHO recommended screen-and-treat options for LMICs, namely HPV screen-and-treat and VIA screen-and-treat.
Between July 2013 and May 2014, during a population-based survey of HPV prevalence, 2508 women aged 18-69 years were invited and underwent collection of cervical cells in Muhima hospital or eight other health centers in Nyarugenge district, Kigali, Rwanda. Study procedures have been described in detail elsewhere . In short, exfoliated cervical cells were obtained from all women using a cytobrush (Rovers Medical Devices, The Netherlands), and were placed in PreservCyt medium (Cytyc-Hologic, Marlborough, MA, USA) for the performance of liquid-based cytology and HPV detection using GP5+/6+−based polymerase chain reaction (PCR) at VU University Medical Center, Amsterdam (see below), the results of which have already been published .
Participants aged ≥ 30 years (or ≥ 25 years if known to be HIV-positive) (n = 1062) were also offered visual inspection at their first study visit. The cervix was visually inspected after application of dilute acetic acid, with results reported according to the IARC criteria . This test is hereafter referred to as “screening VIA” (to differentiate it from VIA triage that was used at a second visit to decide treatment, see below). Furthermore, for a subset of these women for whom their study visit coincided with the implementation of the 2013 Rwandan MoH pilot careHPV screening campaign in the same hospital , a second cervical cell sample was collected with a careBrush and placed in a vial containing collection medium for careHPV testing. A total of 764 women with results for careHPV are the subject of the present report (Fig. 1).
The study had the approval of both the Research Ethical Board of the Rwanda Ministry of Health and the IARC Ethics Committee. Written informed consent was obtained from all study participants.
Samples were tested using the careHPV platform (Qiagen Corporation, Gaithersburg, MD, USA) installed in Muhima Hospital, according to the manufacturer’s instructions. The careHPV test is a validated signal-amplification, rapid batch diagnostic test for the detection of DNA of 13 HR-HPV types (HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68) and HPV66. CareHPV results were communicated as soon as possible to the screening clinic to arrange the follow-up of careHPV-positive women. However, due to the practical logistics, careHPV results were not available on the same day as the initial visit.
Slides for liquid-based cytology were prepared from cell samples in PreservCyt medium using a Thin Prep 3000 processor (Cytyc-Hologic), stained according to manufacturer’s instructions and read at the Department of Pathology at the VU University Medical Center, Amsterdam, the Netherlands. Cytological diagnosis was made according to CISOE-A standards and was translated into the Bethesda 2001 terminology system .
HPV testing by PCR
DNA was extracted from the PreservCyt sample using magnetic beads on a robotic system at the Department of Pathology at the VU University Medical Center, Amsterdam. β-globin PCR analysis was conducted to confirm the presence of human DNA in all specimens  and GP5+/6+−mediated PCR was used to amplify HPV DNA . HPV positivity was assessed by hybridization of PCR products in an enzyme immunoassay with two oligoprobe cocktails that, together, detect 44 HPV types. HPV genotyping was subsequently conducted by reverse-line blot (RLB) hybridization of PCR products as described previously . HR-HPV refers to 13 high-risk HPV types only (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 and 68) . Non-high-risk HPV types are ignored in the current analysis.
Cervical disease assessment
One hundred and seventy seven women who were positive by screening VIA and/or by careHPV and/or for HR-HPV infection by PCR (for which results became available at a later date) were all recalled for a second visit, among whom 148 (84%) attended and 29 (16%) were lost to follow-up (Fig. 1). Six of 587 women negative for the three screening tests were also inadvertently recalled for a second visit.
At the second visit, VIA was again used to triage women for immediate treatment (by cryotherapy, thermocoagulation, or if ineligible, loop electrosurgical excision procedures) or not, according to the protocol of the Rwandan MoH careHPV screening campaign , hereafter referred to as “VIA triage”. In addition, for research purposes only, biopsies were to be taken from all women undergoing VIA triage, either VIA-directed to a visible lesion, or, in the absence of a visible lesion, randomly from 12 o’clock of the squamocolumnar junction, prior to any treatment. Histological confirmation of biopsies was performed at the Department of Pathology at the University Teaching Hospital of Kigali, and all biopsies from women with histological and/or cytological abnormalities were re-read by a specialist (TMD) reported according to LAST criteria  which became the reference diagnosis. Adequate histology results were obtained from 139 (90%) of 154 women who underwent VIA triage at the second visit, among whom 12 cases were diagnosed as hHSIL+ (including 1 invasive squamous cell carcinoma).
Conventional screening indices of cross-sectional accuracy, including sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and their 95% confidence intervals, were calculated primarily against histological HSIL or worse (hHSIL+). Corrected indices were calculated after imputation of missing histology data. In the corrected model, pseudo-observations were created for women without a valid histology result, weighted by the probability of hHSIL+ among women with valid histology outcomes and the same combination of cytology, VIA, careHPV and PCR results [16,17,18]. Hence, in addition to the 12 confirmed hHSIL+, an additional 5 hHSIL+ were estimated among women without a valid histology outcome (Table 1). Only corrected indices are shown, but crude indices assuming that all women without valid histology had no hHSIL+ can also be calculated from the data described in Table 1. As secondary analyses, screening indices were also calculated against the outcome of cytological HSIL or worse (cHSIL+), or against a composite outcome of cytological and/or histological HSIL+ (composite HSIL+).
The performance of VIA, careHPV and PCR were first compared in a hypothetical scenario of single-visit screen-and-treat, treating all test-positive women at the same visit. In this model, the HSIL+ cases (imputed hHSIL+ and/or observed cHSIL+) among the 29 women without a second visit are assumed to be treated.
Secondly, based on the actual 2-visit approach that was used, we compared the Rwandan MoH careHPV screening campaign algorithm of careHPV primary testing at the first visit followed by VIA triage to decide treatment or not, against the counterfactual option of treating all careHPV-positive women at the second visit. In this analysis, the HSIL+ cases among the women without a second visit are lost to follow-up and remain untreated.
Of the 764 screened women, mean age was 43 years [interquartile range = 35-49 years], 84% were literate, 66% were currently married, 56% reported more than one lifetime sexual partner, 35% were known to be HIV-positive, and only 2.6% reported previous attendance to cervical screening (Additional file 1: Table S1).
Table 2 shows indices of cross-sectional accuracy by different primary screening methods, firstly in a 1-visit screen-and-treat scenario. Positivity rate was 5.1% for VIA screen-and-treat, 13.4% for careHPV and 15.7% for PCR. CareHPV showed higher sensitivity against hHSIL+ (71%) than VIA (41%), but lower than that of PCR (88%). NPV was also higher for careHPV (99.2%) than screening VIA (98.6%) but lower than that of PCR (99.7%). Specificity of careHPV (89%), on the other hand, was lower than for screening VIA (95%), and similar to PCR (87%). PPV for hHSIL+ was highest for screening VIA (17%).
Table 2 also shows screening indices of cross-sectional accuracy based on a 2-visit approach, i.e., HPV primary screening followed by referral of all HPV-positive women for treatment, in which 29 women were lost to follow-up and would not be treated even if screen-positive. Treating all careHPV positive women in a 2-visit approach resulted in the treatment of 11.6% of women and was associated with a sensitivity of 59% against hHSIL+. Using VIA to triage careHPV-positives at the second visit resulted in the treatment of only 2.9% of women, but was associated with a drop in sensitivity to 35%.
A similar drop in sensitivity was observed for using VIA to triage PCR-positives in a 2-visit approach, from 73% for treatment of all PCR-positives, down to 47%. Of note, PCR also provided information on HPV genotype: 8 of the 11 PCR-positive hHSIL+ observed at the second visit were HPV16/18-positive (6 HPV16, 2 HPV18), of which 5 (62%) were VIA triaged to no treatment.
Relative performances of the different testing approaches were consistent when using cytological HSIL+ (cHSIL+) (Additional file 1: Table S2), or a composite cytological/histological HSIL+ endpoint (Additional file 1: Table S3), instead of hHSIL+. Furthermore, relative performances against hHSIL+ were also consistent in sensitivity analyses restricted to women aged 25-44 years only (Additional file 1: Table S4).
This evaluation of the performance of the 2013 Rwandan MoH cervical cancer screening campaign is the first real-world comparison of the three options endorsed by the 2013 WHO guidelines for screening and treatment of precancerous cervical lesions in LMICs. Although careHPV did not perform quite as well as a reference PCR HPV test, a careHPV screen-and-treat approach would have treated more hHSIL+ than VIA screen-and-treat (albeit with a higher treatment rate overall). In the actual 2-visit approach used in Rwanda, necessitated by the inability for rapid turnaround of careHPV results, an unacceptably high proportion of women with HPV-positive hHSIL+ were subsequently lost to follow-up and/or triaged by VIA to no treatment, with a result that the 2-visit approach of careHPV+VIA triage ended up performing similarly to VIA screen-and-treat.
In a 1-visit screen-and-treat approach, sensitivity of careHPV was substantially greater than that of VIA, as shown previously . The 71% estimate of careHPV sensitivity represents that at the beginning of experience with the test platform in Rwanda, and was lower than that reported in previous large evaluations (84-100%) [20,21,22,23,24]. It was also lower than that of a HR-HPV PCR test (GP5+/6+) that was done on the same samples in a reference laboratory. Of note, careHPV was performed on clinician-collected samples in the current study, but has been shown to be similarly applicable to self-collected samples [21, 23, 25,26,27].
Although the initial plan of the Rwandan MoH was to deliver careHPV results on the same day  a 1-visit careHPV screen-and-treat approach proved unfeasible. This was partly due to the time requirement of collection of 90 samples coupled with a 3.5 h testing run, but was also hampered by a high number of invalid runs that required re-testing, which are technical features that are not expected to be shared by all HPV tests. Thus, careHPV-positive women were called back for triage and treatment in a second visit, which was associated with the loss to follow-up of an estimated 13% of careHPV-positive hHSIL+. Of note, the loss to follow-up in our well-supported research program is likely to be lower than in the wider Rwanda MoH campaign, and can be compared to 25-30% in other experiences of recalling HPV-positive women [6,7,8, 28].
The fact that not all careHPV-positive women were treated at the second visit but only those positive by a second VIA triage test, greatly reduced the number of women receiving treatment in Rwanda, from 13% to 3%. However, an important fraction (4 out of 10) careHPV-positive hHSIL+ seen at visit 2 were also triaged to no treatment, so that hHSIL+ sensitivity for careHPV+VIA triage dropped to 35%. These findings confirm those of similar studies in which a HPV + VIA triage algorithm was associated with sensitivity of only 33% for cervical intraepithelial neoplasia (CIN)2+ in Cameroon  and 34% for cHSIL+ in Papua New Guinea . In other settings, the proportion of HPV-positive CIN2+ triaged to no treatment have been reported as 75% , 34%  or, estimated in the presence of verification bias due to lack of systematic biopsies, 18% .
Histologically confirmed HSIL is a more accurate diagnosis of true cervical precancerous lesions than cytological HSIL, and was considered as the gold standard outcome for screening indicators in our analysis. However, histology can also suffer from verification bias when biopsies are not obtained from all screened women. In the present study, we attempted to address this problem by obtaining histology from a high proportion of screen-positive women, by expert review of all biopsies according to recommended criteria , and by imputing underlying hHSIL+ among the few from whom we did not have biopsies. It is gold-standard to obtain biopsies directed by colposcopy, but in the present study, as in other similar evaluations , they were directed by VIA. Nevertheless, we were able to show that screening accuracy indices were consistent when evaluated against the outcome of cHSIL+ detected on liquid-based cytology samples that were collected from all women at the same visit as those for careHPV, and evaluated in The Netherlands blindly to HPV results.
We report on VIA as applied in a low-resource setting during the implementation of a government screening program, which is more likely to reflect real world conditions than those estimated from clinical trials, as VIA is subjective and known to vary in quality according to level of training of personnel. In addition to their previous local training, study health workers were nonetheless provided a refresher course on VIA and thermocoagulation prior to the start of the study. Despite this, the estimate of primary VIA screening sensitivity (41%) fell into the lower range of earlier estimates from similar studies , but comparable to that in other large real world experiences that also included widespread training and quality control [32, 33].
Our evaluation was associated with a number of weaknesses, most notably the small number of cases of hHSIL+, which affected the stability of estimates and prohibited the possibility of performing sub-analyses. For example, a substantial subset (35%) of our study population was HIV-positive. This should not explain the poor sensitivity of VIA, as positivity rate and sensitivity tends to be higher in HIV-positive persons for HPV and VIA alike . Furthermore, our semi-observational study design prohibited the evaluation of whether VIA triage of careHPV positives in a 1-visit approach may have treated a few extra hHSIL+ that were subsequently lost to follow-up. Lastly, performance of the HPV + VIA triage algorithm might have improved if careHPV-positive VIA-negative women had been re-screened for persistent HPV-positivity at one year, according to the initial plan of the pilot screening campaign . We were not able to assess this algorithm as, following the first round of screening, the Rwanda MoH decided not to continue with careHPV-testing.
In summary, our data send a warning against the real-world utility of a 2-visit approach to VIA-triage of HPV-positive women as an algorithm for cervical cancer screening [6,7,8, 29]. Indeed, it appears that investment in HPV-testing to identify women at highest risk of hHSIL+ needs to be coupled with systematic treatment (where possible, in a single visit), to obtain the long term prevention of CIN2+ observed for HPV screen-and-treat approaches in prevention trials . In this pragmatic “HPV screen-and-treat” approach, which has been put into practice in large implementation studies , VIA is still used, not to determine whether to treat or not, but to determine eligibility for cryotherapy/thermocoagulation. Although this approach will treat some women without disease, it will also destroy cells from the cervical squamocolumnar junction where most HPV-related neoplastic lesions originate . Indeed, in a modelling exercise, even with re-screening at one year of HPV-positives, 2-visit VIA-triage of HPV positive women was not a cost effective approach in comparison to treating all HPV-positive women .
In the experience in Rwanda, the losses associated with requirement of a second visit and/or with VIA triage led to a 2-visit approach of careHPV+VIA triage treating a similar number of hHSIL (6 out of 17) as VIA screen-and-treat. Indeed, independently of the current analysis, the Rwanda MoH has decided, for pragmatic reasons, to resort to a recommendation of VIA screen-and-treat for cervical cancer screening for the time being.
Atypical squamous cells of undetermined significance
Cytological high-grade squamous intraepithelial lesions
Cervical intraepithelial neoplasia
Histological high-grade squamous intraepithelial lesions
High-risk human papillomavirus
International Agency for Research on Cancer
Low- and middle-income country
Low-grade squamous intraepithelial lesions
Ministry of Health
Negative predictive value
Polymerase chain reaction
Positive predictive value
Visual inspection with acetic acid
Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C. M R, Parkin DM, Forman D, Bray F. GLOBOCAN 2012 v1.0, Cancer incidence and mortality worldwide: IARC CancerBase no. 11 [internet]. International Agency for Research on Cancer: Lyon; 2013. http://globocan.iarc.fr. Accessed 25 July 2017
Binagwaho A, Ngabo F, Wagner CM, Mugeni C, Gatera M, Nutt CT, et al. Integration of comprehensive women's health programmes into health systems: cervical cancer prevention, care and control in Rwanda. Bull World Health Organ. 2013;91:697–703.
Binagwaho A, Wagner CM, Gatera M, Karema C, Nutt CT, Ngabo F. Achieving high coverage in Rwanda's national human papillomavirus vaccination programme. Bull World Health Organ. 2012;90:623–8.
IARC. Biological agents. IARC Monogr Eval Carcinog Risks Hum. 2012;100B:1–475. http://monographs.iarc.fr/ENG/Monographs/vol100B/index.php. Accessed 25 July 2017
Santesso N, Mustafa RA, Schunemann HJ, Arbyn M, Blumenthal PD, Cain J, et al. World Health Organization guidelines for treatment of cervical intraepithelial neoplasia 2-3 and screen-and-treat strategies to prevent cervical cancer. Int J Gynaecol Obstet. 2016;132:252–8.
Bigoni J, Gundar M, Tebeu PM, Bongoe A, Schafer S, Fokom-Domgue J, et al. Cervical cancer screening in sub-Saharan Africa: a randomized trial of VIA versus cytology for triage of HPV-positive women. Int J Cancer. 2015;137:127–34.
Tebeu PM, Fokom-Domgue J, Crofts V, Flahaut E, Catarino R, Untiet S, et al. Effectiveness of a two-stage strategy with HPV testing followed by visual inspection with acetic acid for cervical cancer screening in a low-income setting. Int J Cancer. 2015;136:E743–50.
Catarino R, Vassilakos P, Scaringella S, Undurraga-Malinverno M, Meyer-Hamme U, Ricard-Gauthier D, et al. Smartphone use for cervical Cancer screening in low-resource countries: a pilot study conducted in Madagascar. PLoS One. 2015;10:e0134309.
Ngabo F, Franceschi S, Baussano I, Umulisa MC, Snijders PJ, Uyterlinde AM, et al. Human papillomavirus infection in Rwanda at the moment of implementation of a national HPV vaccination programme. BMC Infect Dis. 2016;16:225.
Sankaranarayanan R, Wesley R. A practical manual on visual screening for cervical neoplasia. IARC technical publication no. 41. Lyon: IARC Press; 2003.
Bulk S, van Kemenade FJ, Rozendaal L, Meijer CJ. The Dutch CISOE-A framework for cytology reporting increases efficacy of screening upon standardisation since 1996. J Clin Pathol. 2004;57:388–93.
de Roda Husman AM, Snijders PJ, Stel HV, van den Brule AJ, Meijer CJ, Walboomers JM. Processing of long-stored archival cervical smears for human papillomavirus detection by the polymerase chain reaction. Br J Cancer. 1995;72:412–7.
Jacobs MV, Walboomers JM, Snijders PJ, Voorhorst FJ, Verheijen RH, Fransen-Daalmeijer N, et al. Distribution of 37 mucosotropic HPV types in women with cytologically normal cervical smears: the age-related patterns for high-risk and low-risk types. Int J Cancer. 2000;87:221–7.
van den Brule AJ, Pol R, Fransen-Daalmeijer N, Schouls LM, Meijer CJ, Snijders PJ. GP5+/6+ PCR followed by reverse line blot analysis enables rapid and high-throughput identification of human papillomavirus genotypes. J Clin Microbiol. 2002;40:779–87.
Darragh TM, Colgan TJ, Thomas Cox J, Heller DS, Henry MR, Luff RD, et al. The lower Anogenital squamous terminology standardization project for HPV-associated lesions: background and consensus recommendations from the College of American Pathologists and the American Society for Colposcopy and Cervical Pathology. Int J Gynecol Pathol. 2013;32:76–115.
Almonte M, Ferreccio C, Winkler JL, Cuzick J, Tsu V, Robles S, et al. Cervical screening by visual inspection, HPV testing, liquid-based and conventional cytology in Amazonian Peru. Int J Cancer. 2007;121:796–802.
Li N, Shi JF, Franceschi S, Zhang WH, Dai M, Liu B, et al. Different cervical cancer screening approaches in a Chinese multicentre study. Br J Cancer. 2009;100:532–7.
Tshomo U, Franceschi S, Tshokey T, Tobgay T, Baussano I, Tenet V, et al. Evaluation of cytology versus human papillomavirus-based cervical cancer screening algorithms in Bhutan. Oncotarget. 2017;8:72438–46.
Mustafa RA, Santesso N, Khatib R, Mustafa AA, Wiercioch W, Kehar R, et al. Systematic reviews and meta-analyses of the accuracy of HPV tests, visual inspection with acetic acid, cytology, and colposcopy. Int J Gynaecol Obstet. 2016;132:259–65.
Tuerxun G, Yukesaier A, Lu L, Aierken K, Mijiti P, Jiang Y, et al. Evaluation of careHPV, Cervista human papillomavirus, and hybrid capture 2 methods in diagnosing cervical intraepithelial neoplasia grade 2+ in Xinjiang Uyghur women. Oncologist. 2016;21:825–31.
Qiao YL, Sellors JW, Eder PS, Bao YP, Lim JM, Zhao FH, et al. A new HPV-DNA test for cervical-cancer screening in developing regions: a cross-sectional study of clinical accuracy in rural China. Lancet Oncol. 2008;9:929–36.
Asthana S, Labani S. Adjunct screening of cervical or vaginal samples using careHPV testing with pap and aided visual inspection for detecting high-grade cervical intraepithelial neoplasia. Cancer Epidemiol. 2015;39:104–8.
Jeronimo J, Bansil P, Lim J, Peck R, Paul P, Amador JJ, et al. A multicountry evaluation of careHPV testing, visual inspection with acetic acid, and papanicolaou testing for the detection of cervical cancer. Int J Gynecol Cancer. 2014;24:576–85.
Lorenzi AT, Fregnani JH, Possati-Resende JC, Antoniazzi M, Scapulatempo-Neto C, Syrjanen S, et al. Can the careHPV test performed in mobile units replace cytology for screening in rural and remote areas? Cancer Cytopathol. 2016;124:581–8.
Maza M, Alfaro K, Garai J, Velado MM, Gage JC, Castle PE, et al. Cervical cancer prevention in El Salvador (CAPE)-an HPV testing-based demonstration project: changing the secondary prevention paradigm in a lower middle-income country. Gynecol Oncol Rep. 2017;20:58–61.
Labani S, Asthana S. Age-specific performance of careHPV versus Papanicolaou and visual inspection of cervix with acetic acid testing in a primary cervical cancer screening. J Epidemiol Community Health. 2016;70:72–7.
Baussano I, Tshering S, Choden T, Lazzarato F, Tenet V, Plummer M, et al. Cervical cancer screening in rural Bhutan with the careHPV test on self-collected samples: an ongoing cross-sectional, population-based study (REACH-Bhutan). BMJ Open. 2017;7:e016309.
Cremer M, Maza M, Alfaro K, Morales Velado M, Felix J, Castle PE, et al. Scale-up of an human papillomavirus testing implementation program in El Salvador. J Low Genit Tract Dis. 2017;21:26–32.
Toliman P, Philips S, Badman S, Gabuzzi J, Silim S, Forereme L, et al. Pilot study suggests point-of-care HPV testing outperforms either VIA or combination HPV/VIA in Papua New Guinea [abstr]. Cape Town: 31st International Papillomavirus Conference; 2017. p. 2017.
Muwonge R, Wesley RS, Nene BM, Shastri SS, Jayant K, Malvi SG, et al. Evaluation of cytology and visual triage of human papillomavirus-positive women in cervical cancer prevention in India. Int J Cancer. 2014;134:2902–9.
Sauvaget C, Fayette JM, Muwonge R, Wesley R, Sankaranarayanan R. Accuracy of visual inspection with acetic acid for cervical cancer screening. Int J Gynaecol Obstet. 2011;113:14–24.
Gravitt PE, Paul P, Katki HA, Vendantham H, Ramakrishna G, Sudula M, et al. Effectiveness of VIA, pap, and HPV DNA testing in a cervical cancer screening program in a peri-urban community in Andhra Pradesh. India PLoS One. 2010;5:e13711.
Labani S, Asthana S, Sodhani P, Gupta S, Bhambhani S, Pooja B, et al. CareHPV cervical cancer screening demonstration in a rural population of North India. Eur J Obstet Gynecol Reprod Biol. 2014;176:75–9.
Viviano M, DeBeaudrap P, Tebeu PM, Fouogue JT, Vassilakos P, Petignat P. A review of screening strategies for cervical cancer in human immunodeficiency virus-positive women in sub-Saharan Africa. Int J Womens Health. 2017;9:69–79.
Denny L, Kuhn L, Hu CC, Tsai WY, Wright TC Jr. Human papillomavirus-based cervical cancer prevention: long-term results of a randomized screening trial. J Natl Cancer Inst. 2010;102:1557–67.
Herfs M, Yamamoto Y, Laury A, Wang X, Nucci MR, McLaughlin-Drubin ME, et al. A discrete population of squamocolumnar junction cells implicated in the pathogenesis of cervical cancer. Proc Natl Acad Sci U S A. 2012;109:10516–21.
Campos NG, Jeronimo J, Tsu V, Castle PE, Mvundura M, Kim JJ. The cost-effectiveness of visual triage of human papillomavirus-positive women in three low- and middle-income countries. Cancer Epidemiol Biomark Prev. 2017;26:1500–10.
Support for this project came from the International Agency for Research on Cancer and grants from the Bill & Melinda Gates Foundation, USA (grant numbers 35537 and OPP1053353). The funding body had no role in the design of the study, or in the collection, analysis, and interpretation of data; in the writing of the manuscript; or in the decision to submit the manuscript for publication.
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All data generated or analysed during this study are included in this published article or as additional material.
Ethics approval and consent to participate
The study had the approval of both the Research Ethical Board of the Rwanda Ministry of Health and the IARC Ethics Committee. Written informed consent was obtained from all study participants.
PJFS has Honoraria from Speakers Bureau from Roche diagnostics, Gen-Probe, Abbott, Seegene, and Qiagen, and has been a consultant/advisory board member for Crucell BV. DAMH serves occasionally on the scientific advisory board of Pfizer. PJFS and DAMH are minority shareholders of Self-screen B.V., a spin-off company of VUmc which holds patents related to the work. TMD has Honoraria from Roche. The other authors declare that they have no competing interests.
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Additional file 1:
Table S1. Selected characteristics of the study population of 764 women aged 25-69 years. Rwanda 2013-14. Table S2. Sensitivity analysis: screening algorithm accuracy to detect 20 cytological (c) HSIL+ among 764 women aged 25-69 years. Rwanda 2013-14. Table S3. Sensitivity analysis: screening algorithm accuracy to detect 27 composite HSIL+ (cHSIL+ and/or hHSIL+) among 764 women aged 25-69 years. Rwanda 2013-14. Table S4. Sensitivity analysis: screening algorithm accuracy to detect 10 hHSIL+ among 428 women aged 25-44 years, after correction for missing data. Rwanda 2013-14 (DOCX 59 kb)
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Umulisa, M.C., Franceschi, S., Baussano, I. et al. Evaluation of human-papillomavirus testing and visual inspection for cervical cancer screening in Rwanda. BMC Women's Health 18, 59 (2018). https://doi.org/10.1186/s12905-018-0549-5
- Human papillomavirus
- Visual inspection
- Cervical cancer