Julia C Gage

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc Reassurance against future risk of precancer and cancer conferred by a negative human papillomavirus test
    Julia C Gage
    Affiliations of authors Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD JCG, MS, HAK, NW Global Cancer Initiative, Chestertown, MD PEC Regional Laboratory, Kaiser Permanente Northern California, Berkeley, CA BF, NEP, TL Information Management Services Inc, Calverton, MD LCC Division of Gynecologic Oncology, Kaiser Permanente Medical Care Program, Oakland, CA WKK
    J Natl Cancer Inst 106:. 2014
  2. pmc Comparative risk of high-grade histopathology diagnosis after a CIN 1 finding in endocervical curettage versus cervical biopsy
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20892 7234, USA
    J Low Genit Tract Dis 17:137-41. 2013
  3. pmc Risk of precancer determined by HPV genotype combinations in women with minor cytologic abnormalities
    Julia C Gage
    Divisions of Cancer Epidemiology and Genetics and Cancer Prevention National Cancer Institute, Department of Health and Human Services, NIH, Bethesda, MD 20852, USA
    Cancer Epidemiol Biomarkers Prev 22:1095-101. 2013
  4. pmc Effectiveness of a simple rapid human papillomavirus DNA test in rural Nigeria
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA
    Int J Cancer 131:2903-9. 2012
  5. pmc The age-specific prevalence of human papillomavirus and risk of cytologic abnormalities in rural Nigeria: implications for screen-and-treat strategies
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA
    Int J Cancer 130:2111-7. 2012
  6. pmc Comparison of the cobas Human Papillomavirus (HPV) test with the hybrid capture 2 and linear array HPV DNA tests
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, Maryland, USA
    J Clin Microbiol 50:61-5. 2012
  7. pmc Comparative performance of human papillomavirus DNA testing using novel sample collection methods
    Julia C Gage
    Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Blvd, MSC 7231, Rockville, MD 20852, USA
    J Clin Microbiol 49:4185-9. 2011
  8. pmc A comparison of dacron versus Flocked nylon swabs for anal cytology specimen collection
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD 20852, USA
    Acta Cytol 55:364-7. 2011
  9. pmc Detection of cervical cancer and its precursors by endocervical curettage in 13,115 colposcopically guided biopsy examinations
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 6120 Executive Boulevard, Rockville, MD 20892, USA
    Am J Obstet Gynecol 203:481.e1-9. 2010
  10. pmc An evaluation by midwives and gynecologists of treatability of cervical lesions by cryotherapy among human papillomavirus-positive women
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20852, USA
    Int J Gynecol Cancer 19:728-33. 2009

Detail Information

Publications46

  1. pmc Reassurance against future risk of precancer and cancer conferred by a negative human papillomavirus test
    Julia C Gage
    Affiliations of authors Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD JCG, MS, HAK, NW Global Cancer Initiative, Chestertown, MD PEC Regional Laboratory, Kaiser Permanente Northern California, Berkeley, CA BF, NEP, TL Information Management Services Inc, Calverton, MD LCC Division of Gynecologic Oncology, Kaiser Permanente Medical Care Program, Oakland, CA WKK
    J Natl Cancer Inst 106:. 2014
    ..069% vs 0.11%, P < .0001; Cancer = 0.011% vs 0.014%, P = .21). These findings suggest that primary HPV testing merits consideration as another alternative for cervical screening. ..
  2. pmc Comparative risk of high-grade histopathology diagnosis after a CIN 1 finding in endocervical curettage versus cervical biopsy
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20892 7234, USA
    J Low Genit Tract Dis 17:137-41. 2013
    ..For women with these pathologic findings, we assessed their short-term risk of high-grade histopathologic diagnosis in the Calgary Health Region where ECC was routinely performed...
  3. pmc Risk of precancer determined by HPV genotype combinations in women with minor cytologic abnormalities
    Julia C Gage
    Divisions of Cancer Epidemiology and Genetics and Cancer Prevention National Cancer Institute, Department of Health and Human Services, NIH, Bethesda, MD 20852, USA
    Cancer Epidemiol Biomarkers Prev 22:1095-101. 2013
    ..We evaluated genotyping for HPV16, HPV16/18, and HPV16/18/45 in carcinogenic HPV-positive women with atypical squamous cells of undetermined significance (ASCUS) and low-grade squamous intraepithelial lesion (LSIL) cytology...
  4. pmc Effectiveness of a simple rapid human papillomavirus DNA test in rural Nigeria
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA
    Int J Cancer 131:2903-9. 2012
    ..In a challenging low-resource setting with minimal intervention, the careHPV test performed adequately with high specificity but possibly lower sensitivity than HPV DNA tests currently used in controlled situations...
  5. pmc The age-specific prevalence of human papillomavirus and risk of cytologic abnormalities in rural Nigeria: implications for screen-and-treat strategies
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA
    Int J Cancer 130:2111-7. 2012
    ....
  6. pmc Comparison of the cobas Human Papillomavirus (HPV) test with the hybrid capture 2 and linear array HPV DNA tests
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, Maryland, USA
    J Clin Microbiol 50:61-5. 2012
    ..Additional studies are needed to compare HC2 and cobas for detecting and predicting CIN3 to understand the clinical implications of the discrepant test results between the two tests...
  7. pmc Comparative performance of human papillomavirus DNA testing using novel sample collection methods
    Julia C Gage
    Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Blvd, MSC 7231, Rockville, MD 20852, USA
    J Clin Microbiol 49:4185-9. 2011
    ..HC2 is likely more clinically specific, although possibly less sensitive, than either PCR test. Thus, use of HC2 on cervicovaginal specimens for screening could result in fewer referrals compared to LA and Amplicor...
  8. pmc A comparison of dacron versus Flocked nylon swabs for anal cytology specimen collection
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD 20852, USA
    Acta Cytol 55:364-7. 2011
    ..We compared the performance of commonly used Dacron versus flocked nylon swabs for anal cytology...
  9. pmc Detection of cervical cancer and its precursors by endocervical curettage in 13,115 colposcopically guided biopsy examinations
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 6120 Executive Boulevard, Rockville, MD 20892, USA
    Am J Obstet Gynecol 203:481.e1-9. 2010
    ..ECC is routinely performed in the Calgary Health Region colposcopy clinics, permitting a look at its real-world utility...
  10. pmc An evaluation by midwives and gynecologists of treatability of cervical lesions by cryotherapy among human papillomavirus-positive women
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20852, USA
    Int J Gynecol Cancer 19:728-33. 2009
    ..To estimate efficacy of a visual triage of human papillomavirus (HPV)-positive women to either immediate cryotherapy or referral if not treatable (eg, invasive cancer, large precancers)...
  11. pmc Comparison of measurements of human papillomavirus persistence for postcolposcopic surveillance for cervical precancerous lesions
    Julia C Gage
    Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Boulevard, EPS 7013, Rockville, MD 20852, USA
    Cancer Epidemiol Biomarkers Prev 19:1668-74. 2010
    ..Compared with pooled-probe testing, measuring HPV genotype-specific persistence might better predict subsequent grade 3 cervical intraepithelial neoplasia (CIN3)...
  12. pmc Treatability by cryotherapy in a screen-and-treat strategy
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20852, USA
    J Low Genit Tract Dis 13:174-81. 2009
    ..We estimated the percentage of women infected with human papillomavirus (HPV+) who cannot be immediately treated with cryotherapy...
  13. pmc Five-year risk of recurrence after treatment of CIN 2, CIN 3, or AIS: performance of HPV and Pap cotesting in posttreatment management
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S78-84. 2013
    ..It is not clear how many negative posttreatment Pap or cotest results are needed to ensure adequate safety against CIN 2+ before returning to extended retesting intervals...
  14. pmc Follow-up testing after colposcopy: five-year risk of CIN 2+ after a colposcopic diagnosis of CIN 1 or less
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S69-77. 2013
    ..An important question is how many subsequent negative Pap results, or negative Pap and human papillomavirus (HPV) cotest results, are needed before returning to an extended retesting interval...
  15. pmc Risk factors for anal HPV infection and anal precancer in HIV-infected men who have sex with men
    Lauren M Schwartz
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville
    J Infect Dis 208:1768-75. 2013
    ..We evaluated risk factors for HPV infection and anal precancer in a population of HIV-infected MSM...
  16. pmc Five-year risks of CIN 3+ and cervical cancer among women with HPV-positive and HPV-negative high-grade Pap results
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S50-5. 2013
    ..We examined whether HPV testing provides useful risk stratification in this context...
  17. pmc Five-year risks of CIN 2+ and CIN 3+ among women with HPV-positive and HPV-negative LSIL Pap results
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S43-9. 2013
    ..Some authors have suggested that HPV triage might be effective at older ages, when the percentage of HPV positivity among women with LSIL declines...
  18. pmc Five-year risks of CIN 3+ and cervical cancer among women with HPV testing of ASC-US Pap results
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S36-42. 2013
    ..However, despite ample data, the routine clinical performance of HPV testing of women with ASC-US has not been adequately documented...
  19. pmc Five-year risks of CIN 3+ and cervical cancer among women who test Pap-negative but are HPV-positive
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S56-63. 2013
    ..However, the performance of these guidelines in routine clinical practice has not been evaluated...
  20. pmc Five-year risk of CIN 3+ to guide the management of women aged 21 to 24 years
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S64-8. 2013
    ..To inform the management of Pap test abnormalities among women aged 21 to 24 years, who have extremely low cancer risks, we compared risks of CIN 3+ among women aged 21 to 24 versus 25 to 29 years or 30 to 64 years...
  21. pmc Benchmarking CIN 3+ risk as the basis for incorporating HPV and Pap cotesting into cervical screening and management guidelines
    Hormuzd A Katki
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health DHHS, Bethesda, MD 20892, USA
    J Low Genit Tract Dis 17:S28-35. 2013
    ..To promote management that is consistent with accepted practice, new guidelines incorporating cotesting should aim to achieve equal management of women at equal risk of cervical intraepithelial neoplasia grade 3 and cancer (CIN 3+)...
  22. pmc Human papillomavirus genotype attribution and estimation of preventable fraction of anal intraepithelial neoplasia cases among HIV-infected men who have sex with men
    Vikrant V Sahasrabuddhe
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland 20852, USA
    J Infect Dis 207:392-401. 2013
    ....
  23. pmc Human papillomavirus genotypes detected in clinician-collected and self-collected specimens from women living in the Mississippi Delta
    Philip E Castle
    Global Cancer Imitative, Chestertown, MD, USA
    BMC Infect Dis 13:5. 2013
    ..The aim of this analysis was to report the age-specific prevalence of HPV in this population...
  24. pmc Human papillomavirus testing in the prevention of cervical cancer
    Mark Schiffman
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA
    J Natl Cancer Inst 103:368-83. 2011
    ..The greatest potential for reduction in cervical cancer rates from HPV screening is in low-resource regions that can implement infrequent rounds of low-cost HPV testing and treatment...
  25. pmc A pilot analytic study of a research-level, lower-cost human papillomavirus 16, 18, and 45 test
    Hannah P Yang
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, MD 20892 7234, USA
    J Virol Methods 176:112-4. 2011
    ..It is concluded that the HPV16/18/45 assay is a promising triage test with a minimum detection of approximately 5000 viral copies, the clinically relevant threshold...
  26. pmc Human papillomavirus genotyping, human papillomavirus mRNA expression, and p16/Ki-67 cytology to detect anal cancer precursors in HIV-infected MSM
    Nicolas Wentzensen
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20852, USA
    AIDS 26:2185-92. 2012
    ..Both approaches have limited reproducibility and sensitivity for detecting anal cancer precursors. We evaluated biomarkers for human papillomavirus (HPV)-related disease in a population of HIV-infected MSM...
  27. pmc A large, population-based study of age-related associations between vaginal pH and human papillomavirus infection
    Megan A Clarke
    Division of Cancer Epidemiology and Genetics, DHHS, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA
    BMC Infect Dis 12:33. 2012
    ..We examined vaginal pH and the risk of HPV infection, cytological abnormalities, and C. trachomatis infection...
  28. pmc Similar Risk Patterns After Cervical Screening in Two Large U.S. Populations: Implications for Clinical Guidelines
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland the Departments of Pathology, Internal Medicine, and Obstetrics and Gynecology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico Information Management Services Inc, Calverton, Maryland the Centre for Cancer Prevention, Wolfson Institute of Preventive Medicine, Queen Mary University of London, Charterhouse Square, London, United Kingdom the Division of Gynecologic Oncology, Kaiser Permanente Medical Care Program, Oakland, California and the Albert Einstein College of Medicine, New York, New York
    Obstet Gynecol 128:1248-1257. 2016
    ..To compare the risks of histologic high-grade cervical intraepithelial neoplasia (CIN) or worse after different cervical cancer screening test results between two of the largest U.S. clinical practice research data sets...
  29. pmc Age-stratified 5-year risks of cervical precancer among women with enrollment and newly detected HPV infection
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD
    Int J Cancer 136:1665-71. 2015
    ..The CIN3+ risks among older women are sufficiently elevated to warrant continued screening through age 65. ..
  30. pmc A comparison of cervical histopathology variability using whole slide digitized images versus glass slides: experience with a statewide registry
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD 20850, USA
    Hum Pathol 44:2542-8. 2013
    ..Diagnosis of cervical intraepithelial neoplasia differed little between slides and corresponding digitized images. ..
  31. pmc A comparison of human papillomavirus genotype-specific DNA and E6/E7 mRNA detection to identify anal precancer among HIV-infected men who have sex with men
    Philip E Castle
    Albert Einstein College of Medicine, Bronx, NY, USA
    Cancer Epidemiol Biomarkers Prev 22:42-9. 2013
    ..Human papillomavirus (HPV) RNA detection is reportedly more specific for the detection of anogenital precancer than HPV DNA but it is unknown whether this is due to detection of RNA or due to HPV genotype restriction...
  32. pmc The population impact of human papillomavirus/cytology cervical cotesting at 3-year intervals: Reduced cervical cancer risk and decreased yield of precancer per screen
    Michelle I Silver
    Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland
    Cancer 122:3682-3686. 2016
    ..The effect on screening efficiency, defined as numbers of cotests/colposcopy visits needed to detect a precancer, also was considered...
  33. doi request reprint The low risk of precancer after a screening result of human papillomavirus-negative/atypical squamous cells of undetermined significance papanicolaou and implications for clinical management
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland
    Cancer Cytopathol 122:842-50. 2014
    ....
  34. pmc Analytic and clinical performance of cobas HPV testing in anal specimens from HIV-positive men who have sex with men
    Nicolas Wentzensen
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA
    J Clin Microbiol 52:2892-7. 2014
    ..001). We demonstrate that cobas can be used for HPV detection in anal cytology specimens. Additional tests are necessary to identify men at the highest risk of anal cancer among those infected with high-risk HPV...
  35. pmc A population-based study of visual inspection with acetic acid (VIA) for cervical screening in rural Nigeria
    Kayode Olusegun Ajenifuja
    Department of Obstetrics, Gynaecology and Perinatology, Obafemi Awolowo University, Ile Ife, Nigeria
    Int J Gynecol Cancer 23:507-12. 2013
    ..We sought to compare VIA performance among different health workers in Nigeria...
  36. doi request reprint A cohort study of cervical screening using partial HPV typing and cytology triage
    Mark Schiffman
    National Cancer Institute Division of Cancer Epidemiology and Genetics, Rockville, MD
    Int J Cancer 139:2606-15. 2016
    ..Overall, the results support primary HPV testing, with management of HPV-positive women using partial HPV typing and cytology. ..
  37. pmc The Role of Human Papillomavirus Genotyping in Cervical Cancer Screening: A Large-Scale Evaluation of the cobas HPV Test
    Mark Schiffman
    National Cancer Institute, Bethesda, Maryland
    Cancer Epidemiol Biomarkers Prev 24:1304-10. 2015
    ..The test is approved for (i) atypical squamous cells of undetermined significance (ASC-US) triage to determine need for colposcopy, (ii) combined screening with cytology ("cotesting"), and (iii) primary HPV screening...
  38. pmc Risk Stratification Using Human Papillomavirus Testing among Women with Equivocally Abnormal Cytology: Results from a State-Wide Surveillance Program
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, Maryland
    Cancer Epidemiol Biomarkers Prev 25:36-42. 2016
    ..The New Mexico Human Papillomavirus (HPV) Pap Registry offers a unique opportunity to evaluate cervical cancer screening in a diverse population across a broad-spectrum of health service delivery...
  39. pmc A population-based cross-sectional study of age-specific risk factors for high risk human papillomavirus prevalence in rural Nigeria
    Megan A Clarke
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA
    Infect Agent Cancer 6:12. 2011
    ..The goal of this study is to explore risk factors for HR-HPV prevalence by age among women in our population-based study in Irun, a rural town in southwestern Nigeria...
  40. pmc A study of HPV typing for the management of HPV-positive ASC-US cervical cytologic results
    Mark Schiffman
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Rockville, MD, USA Electronic address
    Gynecol Oncol 138:573-8. 2015
    ..We evaluated whether partial typing by Onclarity™ (BD) might identify HPV-positive women with low enough CIN3+ risk to permit 1-year follow-up instead...
  41. pmc Cervical histopathology variability among laboratories: a population-based statewide investigation
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services DHHS, Bethesda, MD, USA
    Am J Clin Pathol 139:330-5. 2013
    ..In conclusion, the frequency of diagnoses requiring special staining (p16(INK4a) immunostaining) to adjudicate equivocal CIN2 will be sizable and vary between laboratories, especially if extended to a fraction of CIN1 lesions...
  42. ncbi request reprint Number of cervical biopsies and sensitivity of colposcopy
    Julia C Gage
    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA
    Obstet Gynecol 108:264-72. 2006
    ..To examine the influence that type of medical training and number of biopsies have on sensitivity of colposcopically guided biopsies...
  43. pmc The clinical meaning of a cervical intraepithelial neoplasia grade 1 biopsy
    Philip E Castle
    American Society for Clinical Pathology Institute, Washington, DC 20005, USA
    Obstet Gynecol 118:1222-9. 2011
    ..To determine whether the diagnosis of cervical intraepithelial neoplasia (CIN) grade 1 increases the risk of CIN 3 above what is observed for human papillomavirus (HPV) infection...
  44. pmc Scale-Up of an Human Papillomavirus Testing Implementation Program in El Salvador
    Miriam Cremer
    1Obstetrics, Gynecology and Women s Health Institute, Cleveland Clinic Lerner College of Medicine, Cleveland, OH 2Basic Health International, San Salvador, El Salvador 3National Unit of Control and Prevention of Cancer, Ministry of Health, San Salvador, El Salvador 4Department of Pathology, University of Southern California, Los Angeles, CA 5Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 6Albert Einstein College of Medicine, Bronx, NY 7Global Coalition Against Cervical Cancer, Arlington VA and 8Center for Health Decision Science, Harvard T H Chan School of Public Health, Boston, MA
    J Low Genit Tract Dis . 2016
    ..Results of phase 2 of the project are presented. The objective of this project was to compare colposcopy and noncolposcopy-based management for HPV-positive women...
  45. ncbi request reprint Follow-up care of women with an abnormal cytology in a low-resource setting
    Julia C Gage
    Health Resources and Services Administration, 5600 Fishers Lane, Room 18 41, Rockville, MD, USA
    Cancer Detect Prev 27:466-71. 2003
    ..We ascertained the follow-up care after an abnormal cytology (Papanicolaou) screening in the San Marti;n region of Perú and assessed the status of women who had not received adequate care...
  46. pmc Introducing a High-Risk HPV DNA Test Into a Public Sector Screening Program in El Salvador
    Miriam L Cremer
    1Basic Health International, San Salvador, El Salvador 2Obstetrics, Gynecology and Women s Health Institute, Cleveland Clinic, Cleveland, OH 3Center for Health Decision Science, Harvard School of Public Health, Boston, MA 4Ministry of Health of El Salvador, San Salvador, El Salvador 5Department of Preventive Medicine, University of Southern California, Children s Oncology Group, Arcadia, CA 6Department of Pathology, University of Southern California, Los Angeles, CA 7Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY and 8Division of Cancer Epidemiology and Genetic, National Cancer Institute, Rockville, MD
    J Low Genit Tract Dis 20:145-50. 2016
    ..In a primary human papillomavirus (HPV) screening program, we compared the 6-month follow-up among colposcopy and noncolposcopy-based management strategies for screen-positive women...