Main Article Content
Abstract
ABSTRACT
Introduction – Aim. Cervical cancer, although largely preventable, remains the most common cause of cancer mortality amongst women in low-resource countries. Epidemiological and clinical studies have clearly established human papillomavirus (HPV) types 16 and 18 as the main cause of invasive cervical cancer (ICC). Despite the high burden of HPV (39.0%), high mortality due to cervical cancer in Cameroon, and availability of vaccines, quality reviews on HPV to inform effective public health control strategies are lacking. Methods. We carried out systematically search of 12 major electronic databases for published articles and grey literature up to May 2016 as per PRISMA guidelines. We included studies without language restriction that reported the prevalence of HPV genotypes 16 and 18 among Cameroonian women. Data was extracted and study quality appraised from 5 articles. Results. Our search strategy resulted in five eligible articles, including a total of 1856 women, age ≥18 years tested for HPV. The overall HPV prevalence in Cameroon observed in our systematic review was 36.3% (673/1856). The prevalence of HPV 16 and 18 were 13.0% and 6.5% in women with normal cytology, 18.2% and 4.6% in ASCUS, 29.7% and 27.0% in HSIL, 22.2% and 5.3% in women with ICC respectively. Conclusion. Our study shows that HPV16 and 18 account for 27.5% of ICC cases among Cameroonian women with a high HPV prevalence in women > 25 years of age. These findings greatly support increased efforts in screening for high risk HPV genotypes and the introduction and roll out of HPV prophylactic vaccines in Cameroon.
RÉSUMÉ
Objectifs. Malgré le fardeau élevé du virus du papillomavirus humain (VPH) (39,0%), la mortalité élevée due au cancer du col de l'utérus au Cameroun et la disponibilité des vaccins, les revues de qualité sur le VPH pour renforcer l'efficacité des stratégies de contrôle en santé publique font défaut. Méthodes. Nous avons fait une revue systématique à la recherche de 12 bases de données électroniques majeures pour les articles publiés et la littérature grise jusqu'en mai 2016, conformément aux lignes directrices de PRISMA. Notre critère d’inclusion était les études sans restriction de langue qui ont signalé la prévalence des génotypes du VPH 16 et 18 parmi les femmes camerounaises. Résultats. Notre stratégie de recherche a abouti à cinq articles éligibles, donnant 1856 femmes, âgées de 18 ans testées pour le VPH. La prévalence globale du VPH au Cameroun observée dans notre étude était de 36,3% (673/1856). VPH 16 et 18 représentaient 6,25% et 3,28% respectivement. La prévalence du VPH 16 et 18 était de 13,0% et 6,5% chez les femmes ayant une cytologie normale et 5,3% chez les femmes avec cancer invasif du col (CIC). Conclusion. Notre étude montre que HPV 16 et 18 représentent 27,5% des cas de CIC chez les femmes camerounaises avec une forte prévalence du VPH chez les femmes > 25 ans. Ces résultats appuient grandement les efforts accrus dans le dépistage des génotypes de HPV à haut risque et l'introduction et le déploiement des vaccins prophylactiques contre le VPH au Cameroun.
Keywords
Article Details
References
- SP Cerón, Shelley L Deeks, LG Dilsa, Domínguez. MC EFD. Prevention. Progress toward implementation of human papillomavirus vaccination—the Americas 2006-2010.2011;60(40) 1382–1384. ISSN: 1545-861X.
- Ferlay, J.; Shin, HR.; Bray, F.; Forman, D.; Mathers, C.; Parkin, DM. GLOBOCAN 2008, v12.Lyon FIA for R on C 2010. Cancer Incidence and Mortality Worldwide. Int J Cancer. 2010;127(11):2893–917. http://globocan.iarc.fr (accessed 14.04.2016).
- Eduard R. Bos, Dean T. Jamison, Florence Bainga, Richard G. A. Feacham, Malegapuru Makgoba KJH and hama OR. Diseases and mortality in Sub-Saharan Africa. 2006. 1-410. http://dx.doi: 10.1596/978-0-8213-6397-3
- Ogembo RK, Gona PN, Seymour AJ, Park HS-M, Bain PA, Maranda L, et al. Prevalence of human papillomavirus genotypes among African women with normal cervical cytology and neoplasia: a systematic review and meta-analysis. PLoS One. 2015;10(4):e0122488. http://dx.doi:10.1371/journal. pone.0122488
- Parkin DM. The global health burden of infection-associated cancers in the year 2002. Int J cancer. 2006;118(12):3030–44. http://dx.doi 10.1002/Ijc.21731
- Emma J. Crosbie, Mark H. Einstein, Silvia Franceschi HCK. Human papillomavirus and cervical cancer. Clin Microbiol Rev. 2003;382(9895):889–99. http://dx.doi.org/10.1016/S0140-6736(13)60022-7
- N Munoz, F X Bosch, S de Sanjose, R Herrero, X Castellsague, K V Shah, P J F Snijders, Cjlm Meijer CIARCM. Epidemiologic classification of human papillomavirus types associated with cervical cancer. N Engl J Med. 2003;348:518–27. http://dx.doi:10.1056/NEJMoa021641
- International Agency for Research on Cancer I. Handbooks on Cancer Prevention, Cervix Cancer Screening. 2005. 201-212. ISBN 92 832 3010 2
- Jemal A, Bray F, Center MM, Ferlay J, Ward E FD. Global cancer statistics. CA: a cancer J Clin. 2011;61(2):69–90. http://dx.doi:10.3322/caac.20107
- Gakidou E, Nordhagen S OZ. Coverage of cervical cancer screening in 57 countries: low average levels and large inequalities. PLoS Med. 2008;5(6):863–8. http://dx.doi: org/10.1371/journal.pmed.0050132
- Baldur-Felskov B, Dehlendorff C, Munk C KS. Early Impact of Human Papillomavirus Vaccination on Cervical Neoplasia—Nationwide Follow-up of Young Danish Women. J Natl Cancer Inst. 2014;106(3):1. http://dx.doi: 10.1093/jnci/djt460
- Sepehr N. Tabrizi, Julia M L Brotherton, John M. Kaldor, S. Rachel Skinner, Eleanor Cummins, Bette Liu, Deborah Bateson, Kathleen McNamee, Maria Garefalakis SMG. Fall in human papillomavirus prevalence following a national vaccination program. J Infect Dis. 2012;206(11):1645–51. http://dx.doi: 10.1093/infdis/jis590
- Agosti JM GS. Introducing HPV vaccine in developing countries, Äîkey challenges and issues. N Engl J Med. 2007;356(19):1908–10. http://dx.doi: 10.1056/NEJMp078053
- Goldie SJ, Gaffikin L, Goldhaber-Fiebert JD, Gordillo-Tobar A, Levin C, Mahé C, et al. Cost-effectiveness of cervical-cancer screening in five developing countries. N Engl J Med. 2005;353(20):2158–68. http://dx.doi: 10.1056/NEJMsa044278
- Perlman S WROJMSNKFL. Achieving High Uptake of Human Papillomavirus Vaccine in Cameroon: Lessons learned in overcoming challenges. J Vaccine. 2014;32(35):4399–403. http://dx.doi: 10.1016/j.vaccine.2014.06.064.
- Perlman S, R G Wamai, P A Bain, T Welty, E Welty, J G Ogembo. Knowledge and Awareness of HPV Vaccine and Acceptability to Vaccinate in Sub-Saharan Africa. PLoS One. 2014;9(3):e90912. http://dx.doi: 10.1371/journal.pone.0090912
- Bhatla N, Lal N, Bao YP, Ng T QY. A meta-analysis of human papillomavirus type distribution in women from South Asia: Implications for vaccination. J Vaccine. 2008;26(23):2811–7. http://dx.doi: 10.1016/j.vaccine.2008.03.047
- Ciapponi A, Bardach A, Glujovsky D, Gibbons L PM. Type-specific HPV prevalence in cervical cancer and high-grade lesions in Latin America and the Caribbean: Systematic Review and Meta-analysis. PLoS One. 2011;10(6):e0025493. http://dx.doi: 10.1371/journal.pone.0025493
- Clifford GM, Gonp ßalves MAG FS. Human papillomavirus types among women infected with HIV: a meta-analysis. AIDS. 2006;20(18):2337–44. http://dx.doi: 10.1097/01.aids.0000253361.63578.14
- de Sanjose S FSGPH-JRLNBL. Human papillomavirus types in 115,789 HPV-positive women: a meta-analysis from cervical infection to cancer. Int J Cancer. 2012;131(10):2349–59. http://dx.doi: 10.1002/ijc.27485
- Li N, Franceschi S, Howell-Jones R, Snijders PJ CG. Human papillomavirus type distribution in 30,848 invasive cervical cancers worldwide: Variation by geographical region, histological type and year of publication. Int J Cancer. 2011;128(4):927–35. http://dx.doi: 10.1002/ijc.25396
- Jennifer S Smith, Lisa Lindsay, Brooke Hoots, Jessica Keys, Silvia Franceschi, Rachel Winer GMC. Human papillomavirus type distribution in invasive cervical cancer and high-grade cervical lesions: A meta-analysis update. Int J cancer. 2007;121(3):621–32. http://dx.doi: 10.1002/ijc.22527
- Tricco A.C., Ng C.H., Gilca V., Anonychuk A., Pham B. BS. Canadian oncogenic human papillomavirus cervical infection prevalence: Systematic review and meta-analysis. BMC Infect Dis. 2011;11(1):235. http://dx.doi: 10.1186/1471-2334-11-235
- Clifford GM, Smith JS, Plummer M, Muñoz N, Franceschi S. Human papillomavirus types in invasive cervical cancer worldwide: a meta-analysis. Br J Cancer [Internet]. 2003;88(1):63–73. http://dx.doi: 10.1038/sj.bjc.6600688
- Clifford GM, Smith JS, Aguado T, Franceschi S. Comparison of HPV type distribution in high-grade cervical lesions and cervical cancer: a meta-analysis. Br J Cancer [Internet]. 2003;89(1):101–5. http://dx.doi.org/10.1038/sj.bjc.6601024
- Tricco AC, Ng CH, Gilca V, Anonychuk A, Pham B, Berliner S. Canadian oncogenic human papillomavirus cervical infection prevalence: Systematic review and meta-analysis. BMC Infect Dis [Internet]. 2011;11(1):1–15. http://dx.doi.org/10.1186/1471-2334-11-235
- Ayissi CA, Wamai RG, Oduwo GO, Perlman S, Welty E, Welty T, et al. Awareness, acceptability and uptake of human papilloma virus vaccine among Cameroonian School-attending female adolescents. J Community Health. 2012;37(6):1127–35. http://dx.doi: 10.1007/s10900-012-9554-z
- Crofts V, Flahault E, Tebeu PM, Untiet S, Fosso GK, Boulvain M, et al. Education efforts may contribute to wider acceptance of human papillomavirus self-sampling. Int J Womens Health. 2015;7:149–54. http://dx.doi: 10.2147/IJWH.S56307
- Wamai RG, Ayissi CA, Oduwo GO, Perlman S, Welty E, Manga S, et al. Assessing the effectiveness of a community-based sensitization strategy in creating awareness about HPV, cervical cancer and HPV vaccine among parents in North West Cameroon. J Community Health. 2012;37(5):917–26. http://dx.doi: 10.1007/s10900-012-9540-5
- Domgue JBF, Tebeu PM, Vassilakos P, Petignat P. Effectiveness of a two-stage strategy with HPV testing followed by visual inspection with acetic acid (VIA) for cervical cancer screening in a low income setting. Asia Pac J Clin Oncol [Internet]. 2014;10:2–3. http://dx.doi: 10.1002/ijc.29250
- Atashili J, Miller WC, Smith JS, Ndumbe PM, Ikomey GM, Eron J, et al. Age trends in the prevalence of cervical squamous intraepithelial lesions among HIV-positive women in Cameroon: a cross-sectional study. Biomedcentral Res Notes [Internet]. BMC Research Notes; 2012;5(1):590. http://dx.doi: 10.1186/1756-0500-5-590
- Atashili J. Cervical precancerous lesions in hiv-positive women in cameroon: prevalence, predictors and potential impact of screening. 2009. UMI Number: 3352931
- Nkegoum B, Belley Priso E, Mbakop a, Gwent Bell E. Precancerous lesions of the uterine cervix in cameroonian women. Cytological and epidemiological aspects of 946 cases. Gynecol Obstet Fertil. 2001;29(1):15–20. PubMed:11217188. ISSN: 1297-9589
- Lancet T. GAVI injects new life into HPV vaccine rollout. Lancet. 2013;381(9879):1688. http://dx.doi: 10.1016/S0140-6736(13)61058-2
- de Sanjosé S, Diaz M, Castellsagué X, Clifford G, Bruni L MN. Worldwide prevalence and genotype distribution of cervical human papillomavirus DNA in women with normal cytology: a meta-analysis. Lancet Infect Dis. 2007;7(7):453–9. http://dx.doi: 10.1016/S1473-3099(07)70158-5
- Nicole G. Campos, Jane J. Kim, Philip E. Castle, Jesse D. Ortendahl, Meredith O'Shea, Mireia Diaz SJG. Health and economic impact of HPV 16/18 vaccination and cervical cancer screening in Eastern Africa. Int J Cancer. 2012;130(11):2672–84. http://dx.doi: 10.1038/sj.bjc.6604462
- GAVI Alliance. GAVI welcomes lower prices for life-saving vaccines. GAVI. 2011; http://www.gavi.org/library/news/press-releases/2011 ( acessed 14.04.2016)
- Kelly R (GAVI). 206,000 more girls to benefit from HPV vaccine with GAVI Alliance support. GAVI. 2015; http://www.gavi.org/library/news/press-releases/2014.( acessed 14.04.2016)
- Schiffman M, Solomon D. Cervical-Cancer Screening with Human Papillomavirus and Cytologie Cotesting. N Engl J Med [Internet]. 2013;369(24):2324–31. http://dx.doi: 10.1056/NEJMcp1210379
- Solomon N NR. The Bethesda System for reporting cervical cytology: definitions, criteria, and explanatory notes: Springe. Springer International Publishing,. 2015. 1-321 p. ISBN-13: 978-0387403588
- Desruisseau AJ, Schmidt-Grimminger D, Welty E. Epidemiology of HPV in HIV-positive and HIV-negative fertile women in cameroon, West Africa. Infect Dis Obstet Gynecol. 2009;10:6. http://dx.doi:10.1155/2009/810596
- Sando Z, McKee T, Claude Pache J, Kemajou H, Folem O, Rubbia – Brandt L, et al. Human Papillomavirus Genotypes in the High Grade Preinvasive Cervical Lesions in Yaounde (Cameroon). Am J Cancer Prev [Internet]. 2013;1(3):20–3. http://dx.doi:10.12691/ajcp-1-3-1
- Jerome Bigoni, Melissa Gundar, Pierre-Marie Tebeu, Adamo Bongoe, Sonja Schafer, Joel Fokom-Domgue, Rosa Catarino, Evelyne Foguem Tincho, Stephanie Bougel PV and PP. 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(1):127–34.http://dx.doi: 10.1002/ijc.29353
- Pirek D, Petignat P, Vassilakos P, Gourmaud J, Pache J-C, Rubbia-Brandt L, et al. Human papillomavirus genotype distribution among Cameroonian women with invasive cervical cancer: a retrospective study. Sexually transmitted infections. 2015. p. 440–4. http://dx.doi: 10.1136/sextrans-2014-051642
- Catarino R, Vassilakos P, Tebeu P-M, Schäfer S, Bongoe A, Petignat P. Risk factors associated with human papillomavirus prevalence and cervical neoplasia among Cameroonian women. Cancer Epidemiol [Internet]. Elsevier Ltd; 2015;40:60–6. http://dx.doi.org/10.1016/j.canep.2015.
- Luff RD. The Bethesda System for reporting cervical/vaginal cytologic diagnoses: Report of the 1991 Bethesda Workshop. Am J Clin Pathol. 1992;98(2):152–154. Doi: http://dx.doi.org/10.1093/ajcp/98.2.152 152-154
- Sellors JW, Lorincz AT, Mahony JB, Mielzynska I, Lytwyn A, Roth P, et al. Comparison of self-collected vaginal, vulvar and urine samples with physician-collected cervical samples for human papillomavirus testing to detect high-grade squamous intraepithelial lesions. Cmaj. 2000;163(5):513–8. PMID:11006761
- DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88. http://dx.doi: 10.1016/0197-2456(86)90046-2
- Smith JS, Melendy A, Rana RK, Pimenta JM. Age-Specific Prevalence of Infection with Human Papillomavirus in Females: A Global Review. J Adolesc Heal. 2008;43(4 SUPPL.):S5–25. http://dx.doi: 10.1016/j.jadohealth.2008.07.009
- Guan P, Howell-Jones R, Li N, Bruni L, De Sanjosé S, Franceschi S, et al. Human papillomavirus types in 115,789 HPV-positive women: A meta-analysis from cervical infection to cancer. Int J Cancer. 2012;131(10):2349–59. http://dx.doi: 10.1002/ijc.27485
- Smith JS, Lindsay L, Hoots B, Keys J, Franceschi S, Winer R, et al. Human papillomavirus type distribution in invasive cervical cancer and high-grade cervical lesions: a meta-analysis update. Int J Cancer [Internet]. 2007;121(3):621–32. http://dx.doi.org/10.1002/ijc.22527
- World Health Organization. WHO | Preparing for the introduction of HPV vaccines [Internet]. World Health Press. 2006. http://www.who.int/reproductivehealth/publications/cancers/RHR_06.11/en/ (accessed 10.05.2016)
- Peres J. For cancers caused by HPV, two vaccines were just the beginning. J Natl Cancer Inst. 2011;103(5):360–2. http://dx.doi: 10.1093/jnci/djr053
- Denny L, Kuhn L, Hu C-C, Tsai W-Y, Wright TC. Human papillomavirus-based cervical cancer prevention: long-term results of a randomized screening trial. J Natl Cancer Inst [Internet]. 2010;102(20):1557–67. http://dx.doi: 10.1093/jnci/djq342
References
SP Cerón, Shelley L Deeks, LG Dilsa, Domínguez. MC EFD. Prevention. Progress toward implementation of human papillomavirus vaccination—the Americas 2006-2010.2011;60(40) 1382–1384. ISSN: 1545-861X.
Ferlay, J.; Shin, HR.; Bray, F.; Forman, D.; Mathers, C.; Parkin, DM. GLOBOCAN 2008, v12.Lyon FIA for R on C 2010. Cancer Incidence and Mortality Worldwide. Int J Cancer. 2010;127(11):2893–917. http://globocan.iarc.fr (accessed 14.04.2016).
Eduard R. Bos, Dean T. Jamison, Florence Bainga, Richard G. A. Feacham, Malegapuru Makgoba KJH and hama OR. Diseases and mortality in Sub-Saharan Africa. 2006. 1-410. http://dx.doi: 10.1596/978-0-8213-6397-3
Ogembo RK, Gona PN, Seymour AJ, Park HS-M, Bain PA, Maranda L, et al. Prevalence of human papillomavirus genotypes among African women with normal cervical cytology and neoplasia: a systematic review and meta-analysis. PLoS One. 2015;10(4):e0122488. http://dx.doi:10.1371/journal. pone.0122488
Parkin DM. The global health burden of infection-associated cancers in the year 2002. Int J cancer. 2006;118(12):3030–44. http://dx.doi 10.1002/Ijc.21731
Emma J. Crosbie, Mark H. Einstein, Silvia Franceschi HCK. Human papillomavirus and cervical cancer. Clin Microbiol Rev. 2003;382(9895):889–99. http://dx.doi.org/10.1016/S0140-6736(13)60022-7
N Munoz, F X Bosch, S de Sanjose, R Herrero, X Castellsague, K V Shah, P J F Snijders, Cjlm Meijer CIARCM. Epidemiologic classification of human papillomavirus types associated with cervical cancer. N Engl J Med. 2003;348:518–27. http://dx.doi:10.1056/NEJMoa021641
International Agency for Research on Cancer I. Handbooks on Cancer Prevention, Cervix Cancer Screening. 2005. 201-212. ISBN 92 832 3010 2
Jemal A, Bray F, Center MM, Ferlay J, Ward E FD. Global cancer statistics. CA: a cancer J Clin. 2011;61(2):69–90. http://dx.doi:10.3322/caac.20107
Gakidou E, Nordhagen S OZ. Coverage of cervical cancer screening in 57 countries: low average levels and large inequalities. PLoS Med. 2008;5(6):863–8. http://dx.doi: org/10.1371/journal.pmed.0050132
Baldur-Felskov B, Dehlendorff C, Munk C KS. Early Impact of Human Papillomavirus Vaccination on Cervical Neoplasia—Nationwide Follow-up of Young Danish Women. J Natl Cancer Inst. 2014;106(3):1. http://dx.doi: 10.1093/jnci/djt460
Sepehr N. Tabrizi, Julia M L Brotherton, John M. Kaldor, S. Rachel Skinner, Eleanor Cummins, Bette Liu, Deborah Bateson, Kathleen McNamee, Maria Garefalakis SMG. Fall in human papillomavirus prevalence following a national vaccination program. J Infect Dis. 2012;206(11):1645–51. http://dx.doi: 10.1093/infdis/jis590
Agosti JM GS. Introducing HPV vaccine in developing countries, Äîkey challenges and issues. N Engl J Med. 2007;356(19):1908–10. http://dx.doi: 10.1056/NEJMp078053
Goldie SJ, Gaffikin L, Goldhaber-Fiebert JD, Gordillo-Tobar A, Levin C, Mahé C, et al. Cost-effectiveness of cervical-cancer screening in five developing countries. N Engl J Med. 2005;353(20):2158–68. http://dx.doi: 10.1056/NEJMsa044278
Perlman S WROJMSNKFL. Achieving High Uptake of Human Papillomavirus Vaccine in Cameroon: Lessons learned in overcoming challenges. J Vaccine. 2014;32(35):4399–403. http://dx.doi: 10.1016/j.vaccine.2014.06.064.
Perlman S, R G Wamai, P A Bain, T Welty, E Welty, J G Ogembo. Knowledge and Awareness of HPV Vaccine and Acceptability to Vaccinate in Sub-Saharan Africa. PLoS One. 2014;9(3):e90912. http://dx.doi: 10.1371/journal.pone.0090912
Bhatla N, Lal N, Bao YP, Ng T QY. A meta-analysis of human papillomavirus type distribution in women from South Asia: Implications for vaccination. J Vaccine. 2008;26(23):2811–7. http://dx.doi: 10.1016/j.vaccine.2008.03.047
Ciapponi A, Bardach A, Glujovsky D, Gibbons L PM. Type-specific HPV prevalence in cervical cancer and high-grade lesions in Latin America and the Caribbean: Systematic Review and Meta-analysis. PLoS One. 2011;10(6):e0025493. http://dx.doi: 10.1371/journal.pone.0025493
Clifford GM, Gonp ßalves MAG FS. Human papillomavirus types among women infected with HIV: a meta-analysis. AIDS. 2006;20(18):2337–44. http://dx.doi: 10.1097/01.aids.0000253361.63578.14
de Sanjose S FSGPH-JRLNBL. Human papillomavirus types in 115,789 HPV-positive women: a meta-analysis from cervical infection to cancer. Int J Cancer. 2012;131(10):2349–59. http://dx.doi: 10.1002/ijc.27485
Li N, Franceschi S, Howell-Jones R, Snijders PJ CG. Human papillomavirus type distribution in 30,848 invasive cervical cancers worldwide: Variation by geographical region, histological type and year of publication. Int J Cancer. 2011;128(4):927–35. http://dx.doi: 10.1002/ijc.25396
Jennifer S Smith, Lisa Lindsay, Brooke Hoots, Jessica Keys, Silvia Franceschi, Rachel Winer GMC. Human papillomavirus type distribution in invasive cervical cancer and high-grade cervical lesions: A meta-analysis update. Int J cancer. 2007;121(3):621–32. http://dx.doi: 10.1002/ijc.22527
Tricco A.C., Ng C.H., Gilca V., Anonychuk A., Pham B. BS. Canadian oncogenic human papillomavirus cervical infection prevalence: Systematic review and meta-analysis. BMC Infect Dis. 2011;11(1):235. http://dx.doi: 10.1186/1471-2334-11-235
Clifford GM, Smith JS, Plummer M, Muñoz N, Franceschi S. Human papillomavirus types in invasive cervical cancer worldwide: a meta-analysis. Br J Cancer [Internet]. 2003;88(1):63–73. http://dx.doi: 10.1038/sj.bjc.6600688
Clifford GM, Smith JS, Aguado T, Franceschi S. Comparison of HPV type distribution in high-grade cervical lesions and cervical cancer: a meta-analysis. Br J Cancer [Internet]. 2003;89(1):101–5. http://dx.doi.org/10.1038/sj.bjc.6601024
Tricco AC, Ng CH, Gilca V, Anonychuk A, Pham B, Berliner S. Canadian oncogenic human papillomavirus cervical infection prevalence: Systematic review and meta-analysis. BMC Infect Dis [Internet]. 2011;11(1):1–15. http://dx.doi.org/10.1186/1471-2334-11-235
Ayissi CA, Wamai RG, Oduwo GO, Perlman S, Welty E, Welty T, et al. Awareness, acceptability and uptake of human papilloma virus vaccine among Cameroonian School-attending female adolescents. J Community Health. 2012;37(6):1127–35. http://dx.doi: 10.1007/s10900-012-9554-z
Crofts V, Flahault E, Tebeu PM, Untiet S, Fosso GK, Boulvain M, et al. Education efforts may contribute to wider acceptance of human papillomavirus self-sampling. Int J Womens Health. 2015;7:149–54. http://dx.doi: 10.2147/IJWH.S56307
Wamai RG, Ayissi CA, Oduwo GO, Perlman S, Welty E, Manga S, et al. Assessing the effectiveness of a community-based sensitization strategy in creating awareness about HPV, cervical cancer and HPV vaccine among parents in North West Cameroon. J Community Health. 2012;37(5):917–26. http://dx.doi: 10.1007/s10900-012-9540-5
Domgue JBF, Tebeu PM, Vassilakos P, Petignat P. Effectiveness of a two-stage strategy with HPV testing followed by visual inspection with acetic acid (VIA) for cervical cancer screening in a low income setting. Asia Pac J Clin Oncol [Internet]. 2014;10:2–3. http://dx.doi: 10.1002/ijc.29250
Atashili J, Miller WC, Smith JS, Ndumbe PM, Ikomey GM, Eron J, et al. Age trends in the prevalence of cervical squamous intraepithelial lesions among HIV-positive women in Cameroon: a cross-sectional study. Biomedcentral Res Notes [Internet]. BMC Research Notes; 2012;5(1):590. http://dx.doi: 10.1186/1756-0500-5-590
Atashili J. Cervical precancerous lesions in hiv-positive women in cameroon: prevalence, predictors and potential impact of screening. 2009. UMI Number: 3352931
Nkegoum B, Belley Priso E, Mbakop a, Gwent Bell E. Precancerous lesions of the uterine cervix in cameroonian women. Cytological and epidemiological aspects of 946 cases. Gynecol Obstet Fertil. 2001;29(1):15–20. PubMed:11217188. ISSN: 1297-9589
Lancet T. GAVI injects new life into HPV vaccine rollout. Lancet. 2013;381(9879):1688. http://dx.doi: 10.1016/S0140-6736(13)61058-2
de Sanjosé S, Diaz M, Castellsagué X, Clifford G, Bruni L MN. Worldwide prevalence and genotype distribution of cervical human papillomavirus DNA in women with normal cytology: a meta-analysis. Lancet Infect Dis. 2007;7(7):453–9. http://dx.doi: 10.1016/S1473-3099(07)70158-5
Nicole G. Campos, Jane J. Kim, Philip E. Castle, Jesse D. Ortendahl, Meredith O'Shea, Mireia Diaz SJG. Health and economic impact of HPV 16/18 vaccination and cervical cancer screening in Eastern Africa. Int J Cancer. 2012;130(11):2672–84. http://dx.doi: 10.1038/sj.bjc.6604462
GAVI Alliance. GAVI welcomes lower prices for life-saving vaccines. GAVI. 2011; http://www.gavi.org/library/news/press-releases/2011 ( acessed 14.04.2016)
Kelly R (GAVI). 206,000 more girls to benefit from HPV vaccine with GAVI Alliance support. GAVI. 2015; http://www.gavi.org/library/news/press-releases/2014.( acessed 14.04.2016)
Schiffman M, Solomon D. Cervical-Cancer Screening with Human Papillomavirus and Cytologie Cotesting. N Engl J Med [Internet]. 2013;369(24):2324–31. http://dx.doi: 10.1056/NEJMcp1210379
Solomon N NR. The Bethesda System for reporting cervical cytology: definitions, criteria, and explanatory notes: Springe. Springer International Publishing,. 2015. 1-321 p. ISBN-13: 978-0387403588
Desruisseau AJ, Schmidt-Grimminger D, Welty E. Epidemiology of HPV in HIV-positive and HIV-negative fertile women in cameroon, West Africa. Infect Dis Obstet Gynecol. 2009;10:6. http://dx.doi:10.1155/2009/810596
Sando Z, McKee T, Claude Pache J, Kemajou H, Folem O, Rubbia – Brandt L, et al. Human Papillomavirus Genotypes in the High Grade Preinvasive Cervical Lesions in Yaounde (Cameroon). Am J Cancer Prev [Internet]. 2013;1(3):20–3. http://dx.doi:10.12691/ajcp-1-3-1
Jerome Bigoni, Melissa Gundar, Pierre-Marie Tebeu, Adamo Bongoe, Sonja Schafer, Joel Fokom-Domgue, Rosa Catarino, Evelyne Foguem Tincho, Stephanie Bougel PV and PP. 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(1):127–34.http://dx.doi: 10.1002/ijc.29353
Pirek D, Petignat P, Vassilakos P, Gourmaud J, Pache J-C, Rubbia-Brandt L, et al. Human papillomavirus genotype distribution among Cameroonian women with invasive cervical cancer: a retrospective study. Sexually transmitted infections. 2015. p. 440–4. http://dx.doi: 10.1136/sextrans-2014-051642
Catarino R, Vassilakos P, Tebeu P-M, Schäfer S, Bongoe A, Petignat P. Risk factors associated with human papillomavirus prevalence and cervical neoplasia among Cameroonian women. Cancer Epidemiol [Internet]. Elsevier Ltd; 2015;40:60–6. http://dx.doi.org/10.1016/j.canep.2015.
Luff RD. The Bethesda System for reporting cervical/vaginal cytologic diagnoses: Report of the 1991 Bethesda Workshop. Am J Clin Pathol. 1992;98(2):152–154. Doi: http://dx.doi.org/10.1093/ajcp/98.2.152 152-154
Sellors JW, Lorincz AT, Mahony JB, Mielzynska I, Lytwyn A, Roth P, et al. Comparison of self-collected vaginal, vulvar and urine samples with physician-collected cervical samples for human papillomavirus testing to detect high-grade squamous intraepithelial lesions. Cmaj. 2000;163(5):513–8. PMID:11006761
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88. http://dx.doi: 10.1016/0197-2456(86)90046-2
Smith JS, Melendy A, Rana RK, Pimenta JM. Age-Specific Prevalence of Infection with Human Papillomavirus in Females: A Global Review. J Adolesc Heal. 2008;43(4 SUPPL.):S5–25. http://dx.doi: 10.1016/j.jadohealth.2008.07.009
Guan P, Howell-Jones R, Li N, Bruni L, De Sanjosé S, Franceschi S, et al. Human papillomavirus types in 115,789 HPV-positive women: A meta-analysis from cervical infection to cancer. Int J Cancer. 2012;131(10):2349–59. http://dx.doi: 10.1002/ijc.27485
Smith JS, Lindsay L, Hoots B, Keys J, Franceschi S, Winer R, et al. Human papillomavirus type distribution in invasive cervical cancer and high-grade cervical lesions: a meta-analysis update. Int J Cancer [Internet]. 2007;121(3):621–32. http://dx.doi.org/10.1002/ijc.22527
World Health Organization. WHO | Preparing for the introduction of HPV vaccines [Internet]. World Health Press. 2006. http://www.who.int/reproductivehealth/publications/cancers/RHR_06.11/en/ (accessed 10.05.2016)
Peres J. For cancers caused by HPV, two vaccines were just the beginning. J Natl Cancer Inst. 2011;103(5):360–2. http://dx.doi: 10.1093/jnci/djr053
Denny L, Kuhn L, Hu C-C, Tsai W-Y, Wright TC. Human papillomavirus-based cervical cancer prevention: long-term results of a randomized screening trial. J Natl Cancer Inst [Internet]. 2010;102(20):1557–67. http://dx.doi: 10.1093/jnci/djq342