Optimal Strategy for the Management of ASCUS Cytology in Health Care Services of Medellin, Colombia

NCT02067468 — Not applicable, Completed, 2661 participants, Universidad de Antioquia

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Evaluation of Strategies for Optimal Clinical Management of Women With Atypical Squamous Cells of Undetermined Significance (ASC-US)

RegistryNCT02067468, acronym ASCUS-COL
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, health services research
Enrollment2661 (Actual)
SponsorUniversidad de Antioquia (Other); collaborators: International Agency for Research on Cancer, Barts and the London School of Medicine and Dentistry, Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS), QIAGEN Gaithersburg, Inc, EPS SURA, EPS COMFAMA, EPS COMFENALCO, DINAMICA IPS, Laboratorio Clínico Escuela de Microbiología (Universidad de Antioquia), Metrosalud
ConditionsCervical Abnormalities, Cervical Intraepithelial Neoplasia Grade 2/3, Cervical Cancer
InterventionsHPV test, COLPOSCOPY, cytology (Device, procedure)
Datesstart 2011-01-01, primary completion 2016-04-01, completion 2016-04-01, first posted 2014-02-20, last updated 2019-09-19
Locations1 site in Colombia

Related Papers Related Patents Related Grants Related Experts
All trials for Cervical Abnormalities All trials for Cervical Intraepithelial Neoplasia Grade 2/3 All trials of HPV test All trials of COLPOSCOPY

-Summary

Cervical cancer as well cervical preneoplastic abnormalities (CIN2+) are cause by human papillomavirus (HPV) infection. These abnormalities have been historically detected by cervical cytology, but recent evidence shows that HPV testing is superior to cytology to detect cervical lesions that eventually will progress to cancer. Despite evidence, conventional cytology (Pap) remains as a primary screening test in Colombia and HPV test is recommended as a triage test for women with atypical squamous cells of undetermined significance (ASC-US) in settings around the world. Women with ASC-US have low risk to CIN2+ but higher than healthy population, and therefore it is important to provide appropriate clinical management. However, there is no consensus of how to deal women with ASC-US and therefore there are still three strategies for this purpose: 1) immediate colposcopy, 2) repeat conventional cytology at 6 and 12 months and 3) HPV testing. The main objective of this study is to compare the effectiveness and the efficient among the strategies as well as to evaluate the acceptability of the HPV testing in a real-life setting.

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+Detailed description

The aim of this study is to compare the effectiveness and efficiency of immediate colposcopy (IC), repeat conventional cytology at 6 and 12 months (RC) and HPV triage (HPV) (QIAGEN-The digene HPV Test®) for the clinical management of women with ASC-US insured in healthcare management organizations (HMO) within the Colombian health security system. This study randomized 2,661 20-69 years old women with ASC-US, insured in HMOs in Medellin-Colombia to 3 arms: IC, RC and HPV. All women are scheduled for a visit at 2 years after recruitment that includes HPV-test/cytology and colposcopy either if HPV+ (RLU>=1) or abnormal cytology (>=ASC-US). This colposcopy is performed by a trained colposcopist and women are followed-up according to a well-defined algorithm. The fewer high-grade cervical neoplasia (CIN2+) rate at the end of following will determine the most effective arm. The most efficiency arm will be which reach the major effective with the minimum resource (cytologies, colposcopies and histologies) consumed. The resource consumed is being retrieved from the HMOs. This study also pretends to evaluate the acceptability of the HPV testing. This study will allow us to know if within the Colombian health security system, the HPV test will remain superior to repeating cytology and/or to immediate colposcopy as it has been demonstrated in randomized controlled trials carried out in outside settings.

+Arms and interventions

ArmTypeInterventionsDescription
HPV testExperimentalDevice: HPV test; Procedure: COLPOSCOPYWomen with ASC-US cytology are HPV tested and those HPV positive are refer to Colposcopy
COLPOSCOPYActive comparatorProcedure: COLPOSCOPYWomen with ASC-US cytology are immediately refer to colposcopy
CYTOLOGYActive comparatorProcedure: COLPOSCOPY; Device: cytologyWomen with ASC-US Cytology are follow-up with cytology at 6 and/or 12 months and be referred to colposcopy if any of these cytologies is ASC-US or higher
  • HPV test (Device), also known as Human Papillomavirus test, DNA HPV test, High risk HPV test: QIAGEN - The Digene HPV test®
  • COLPOSCOPY (Procedure): Colposcopy routine health services
  • cytology (Device), also known as Pap smear, Papanicolaou test, cervical cytology: Cytology routine health services

+Outcome measures

Primary outcomes

  • Cumulative Number of Participants Diagnosed by the Community Pathologist With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Community-based CIN2+" [Two years since the enrolment to the exit visit (inclusive)]: Cumulative Cervical Intraepithelial Neoplasia Grade 2 or higher (CIN2+) diagnosed by the community pathologists during the two years of follow-up. The first community-based CIN2+ diagnosis was adjudicated to the participant (including the exit visit if none community-based CIN2+ during the two years of follow-up). This outcome is used for the effectiveness analysis of the three strategies.

Secondary outcomes

  • Cumulative Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Reviewed CIN2+" [Two years since the enrolment to the exit visit (inclusive)]: Cumulative Cervical Intraepithelial Neoplasia Grade 2 or higher (CIN2+) diagnosed by a panel of external experts obtained after histological review of biopsies emitted by the community pathologists. Biopsies obtained during the two years of follow-up and the exit visit were reviewed by a panel of two external experts and a final result was adjudicated to each participant based on the panel of experts and the community of pathologists. This outcome is used for the effectiveness analysis of the three strategies.
  • Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+) at the Exit Visit, Two Years After the Enrolment: "Exit-reviewed CIN2+" [Exit visit (two years after the enrolment)]: Cervical Intraepithelial Neoplasia Grade 2 or higher (CIN2+) diagnosed by a panel of external experts after reviewing biopsies collected at the exit visit, two years after the enrolment. This outcome is an estimate of the remaining disease that was not detected by the strategies during the 2 years of follow-up. The outcome was obtained after the review of all the biopsies taken during the exit visit. Biopsies were taken using a standardized research protocol to ensure the completeness of the remaining disease. Basically, all women attending the exit visit were tested with HPV testing and Pap and referred to colposcopy if any HPV positive or abnormal cytology. The colposcopy was performed by a researcher of the study team who took up to two biopsies from the observed lesion plus one or two at random if none lesion was observed. All biopsies were reviewed by the external panel. This outcome is used for the efficiency analysis of the three strategies.
  • Number of Clinical Records (Cytologies, Colposcopies, and Histologies): "Health Care Utilization" [Two years since the enrolment to before the exit visit (i.e., excluding clinical records collected at the exit visit)]: The outcome is defined as the number of cytologies, colposcopies, and histologies routinely performed during the two years of follow-up. Records were identified in databases or manually searched from clinical records. This outcome will be used for the analysis of the efficiency of the three strategies.
  • Self-esteem [Two years between the enrolment and the exit visit]: Self-esteem corresponds to the self-assessment of a positive or negative evaluation toward oneself. This outcome was measured using the Rosenberg Scale through 10 Likert-type questions with scores varying between 1 and 4 (1=strongly agree, 2=agree, 3=disagree, 4=strongly disagree). Total values range between 10 and 40 where lower scores suggest lower self-esteem. This outcome was measured at the enrollment visit, between two weeks and two months after receiving the triage result, and after one year of receiving the triage result.
  • Trait Anxiety [Two years between the enrolment and the exit visit]: Trait anxiety refers to the sustainable tendency to experience negative emotions (such as fears, worries, and anxiety) in various situations. This outcome was measured using the Spielberger State-Trait-Anxiety Inventory (STAI) through 20 Likert-type questions with scores varying between 0 and 3 (0=not at all, 1=somewhat, 2=moderately, 3=very much). Total values range between 0 and 60 where higher scores suggest higher levels of anxiety. This outcome was measured at the enrollment visit, between two weeks and two months after receiving the triage result, and after one year of receiving the triage result.
  • State Anxiety [Two years between the enrolment and the exit visit]: State anxiety refers to the transitory tendency to experience negative emotions (such as fears, worries, and anxiety). This outcome was measured using the Spielberger State-Trait-Anxiety Inventory (STAI) through 20 Likert-type questions with scores varying between 0 and 3 (0=not at all, 1=somewhat, 2=moderately, 3=very much). Total values range between 0 and 60 where higher scores suggest higher levels of anxiety. This outcome was measured at the enrollment visit, between two weeks and two months after receiving the triage result, and after one year of receiving the triage result.
  • Concerns About Fertility, Cancer, and Gynecological Health [Two years between the enrolment and the exit visit]: This outcome was measured using the HPV Impact Profile (HIP) scale through the following five domains: concerns about cancer and loss of fertility; emotional impact (depression and anxiety); self-image; interaction with the medical staff (pain or discomfort during the visit); and impact upon the life and its control. The response to each domain was measured on a scale from 0 to 10 (0=not at all, 1-3=a little, 4-6=somewhat, 7-9=a great deal, 10=extremely) and was then transformed to a scale from 0 to 100. A total score was calculated by adding all the items. Values <40 indicate no or little impact, between 40 and 70 moderate impact, and >70 indicate high psychosocial impact. This outcome was measured at the enrollment visit, between two weeks and two months after receiving the triage result, and after one year of receiving the triage result.

+Eligibility

Sex: Female, ages: 20 Years to 69 Years

Inclusion Criteria:

* ASC-US cytology, living in metropolitan area of Medellin

Exclusion Criteria:

* Previous abnormal cytology

+Posted results

Participant flow

MilestoneCOLPOSCOPYCYTOLOGYHPV Test
Started882890889
Followed-up through medical records882890889
Had at least one routine colposcopy772372462
Completed882890889
Not completed000

Outcome results

  • Cumulative Number of Participants Diagnosed by the Community Pathologist With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Community-based CIN2+" (Primary), Count of participants, Participants: COLPOSCOPY 847; CYTOLOGY 835; HPV Test 848
  • Cumulative Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Reviewed CIN2+" (Secondary), Count of participants, Participants: COLPOSCOPY 813; CYTOLOGY 809; HPV Test 827
  • Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+) at the Exit Visit, Two Years After the Enrolment: "Exit-reviewed CIN2+" (Secondary), Count of participants, Participants: COLPOSCOPY 852; CYTOLOGY 851; HPV Test 866
  • Number of Clinical Records (Cytologies, Colposcopies, and Histologies): "Health Care Utilization" (Secondary), Number, Clinical records: COLPOSCOPY 904; CYTOLOGY 1218; HPV Test 816
  • Self-esteem (Secondary), Mean, score on a scale: COLPOSCOPY 32.9 +/- 4.40; CYTOLOGY 33.0 +/- 4.25; HPV Test 32.8 +/- 4.17
  • Trait Anxiety (Secondary), Mean, score on a scale: COLPOSCOPY 17.5 +/- 13.27; CYTOLOGY 17.4 +/- 11.34; HPV Test 17.7 +/- 11.10
  • State Anxiety (Secondary), Mean, score on a scale: COLPOSCOPY 15.3 +/- 13.23; CYTOLOGY 13.6 +/- 11.03; HPV Test 14.3 +/- 11.45
  • Concerns About Fertility, Cancer, and Gynecological Health (Secondary), Mean, score on a scale: COLPOSCOPY 35.3 +/- 15.23; CYTOLOGY 38.1 +/- 15.45; HPV Test 36.0 +/- 14.72

Adverse events

Time frame: Since the enrolment to the exit visit (2 years after the enrolment)

ArmDeathsSerious adverse eventsOther adverse events
COLPOSCOPY0/882 (0.0%)0/882 (0.0%)0/882 (0.0%)
CYTOLOGY0/890 (0.0%)0/890 (0.0%)0/890 (0.0%)
HPV Test0/889 (0.0%)0/889 (0.0%)0/889 (0.0%)

+Locations (1)

FacilityCityCountryStatus
Universidad de AntioquiaMedellín, AntioquiaColombia

+Publications

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  • ASCUS-LSIL Traige Study (ALTS) Group. Results of a randomized trial on the management of cytology interpretations of atypical squamous cells of undetermined significance. Am J Obstet Gynecol. 2003 Jun;188(6):1383-92. doi: 10.1067/mob.2003.457. PMID 12824967
  • Andres-Gamboa O, Chicaiza L, Garcia-Molina M, Diaz J, Gonzalez M, Murillo R, Ballesteros M, Sanchez R. Cost-effectiveness of conventional cytology and HPV DNA testing for cervical cancer screening in Colombia. Salud Publica Mex. 2008 Jul-Aug;50(4):276-85. doi: 10.1590/s0036-36342008000400005. PMID 18670718
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  • Kulasingam SL, Kim JJ, Lawrence WF, Mandelblatt JS, Myers ER, Schiffman M, Solomon D, Goldie SJ; ALTS Group. Cost-effectiveness analysis based on the atypical squamous cells of undetermined significance/low-grade squamous intraepithelial lesion Triage Study (ALTS). J Natl Cancer Inst. 2006 Jan 18;98(2):92-100. doi: 10.1093/jnci/djj009. PMID 16418511
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  • Instituto Nacional de C. Recomendaciones para el tratamiento de las pacientes con citologia reportada con células escamosas atipicas de significado indeterminado (ASC-US) en Colombia. Guias de practica clinica (No. 2). Bogota, Colombia: INC, 2007
  • Results publication: Baena A, Agudelo MC, Posada G, Lopez C, Buitrago CA, Suescun D, Gomez LJ, Ochoa JC, Sasieni P, Almonte M, Herrero R, Sanchez GI. Efectividad de tres estrategias para el manejo clínico de la citología ASC-US en servicios rutinarios de salud de Medellín, Colombia: diseño y resultados de dos años de seguimiento del ensayo pragmático aleatorio ASCUS-COL (NCT02067468). Rev Colomb Cancerol 2017;21:49 - DOI: 10.1016/j.rccan.2017.02.012
  • Results publication: Baena A, Agudelo MC, Posada G, Lopez C, Buitrago CA, Suescun D, Gomez LJ, Ochoa JC, Sasieni P, Almonte M, Herrero R, Sanchez GI. EI triage con prueba de VPH de aIto riesgo y Ia citoIogía repetida son estrategias eficientes para eI manejo cIínico de mujeres con citoIogía ASC-US en servicios rutinarios de saIud de MedeIIín, CoIombia: resuItados finaIes deI ensayo pragmático aIeatorio ASCUS-COL. Rev Colomb Cancerol 2017;21:49-50 - DOI: 10.1016/j.rccan.2017.02.013
  • Results publication: Urrea Cosme Y, Cordoba Sanchez V, Sanchez GI, Baena A, Ruiz Osorio MA, Rodriguez Zabala D, Garces-Palacio IC. Health-related quality of life of women after HPV testing as triage strategy for an abnormal Pap smear: a nested randomized pragmatic trial in a middle-income country. Qual Life Res. 2020 Nov;29(11):2999-3008. doi: 10.1007/s11136-020-02563-w. Epub 2020 Jul 2. PMID 32617889
  • Results publication: Henao AR, Gomez NEM, Gonzalez-Gomez D, Garces-Palacio IC. Validation of Spanish version of the human papilloma virus impact profile (HIP). Curr Med Res Opin. 2020 Apr;36(4):705-712. doi: 10.1080/03007995.2020.1729709. Epub 2020 Mar 6. PMID 32049551

+Investigators