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Optimal Strategy for the Management of ASCUS Cytology in Health Care Services of Medellin, Colombia (ASCUS-COL)

Primary Purpose

Cervical Abnormalities, Cervical Intraepithelial Neoplasia Grade 2/3, Cervical Cancer

Status
Completed
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
HPV test
COLPOSCOPY
cytology
Sponsored by
Universidad de Antioquia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Cervical Abnormalities focused on measuring Human Papillomavirus, cervical cancer, health services research, Colombia, Cervical Intraepithelial Neoplasia

Eligibility Criteria

20 Years - 69 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  • Previous abnormal cytology

Sites / Locations

  • Universidad de Antioquia

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

HPV test

COLPOSCOPY

CYTOLOGY

Arm Description

Women with ASC-US cytology are HPV tested and those HPV positive are refer to Colposcopy

Women with ASC-US cytology are immediately refer to colposcopy

Women 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

Outcomes

Primary Outcome Measures

Cumulative Number of Participants Diagnosed by the Community Pathologist With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Community-based CIN2+"
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 Outcome Measures

Cumulative Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Reviewed CIN2+"
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+"
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"
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
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
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
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
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.

Full Information

First Posted
February 18, 2014
Last Updated
September 18, 2019
Sponsor
Universidad de Antioquia
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
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1. Study Identification

Unique Protocol Identification Number
NCT02067468
Brief Title
Optimal Strategy for the Management of ASCUS Cytology in Health Care Services of Medellin, Colombia
Acronym
ASCUS-COL
Official Title
Evaluation of Strategies for Optimal Clinical Management of Women With Atypical Squamous Cells of Undetermined Significance (ASC-US)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Antioquia
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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Abnormalities, Cervical Intraepithelial Neoplasia Grade 2/3, Cervical Cancer
Keywords
Human Papillomavirus, cervical cancer, health services research, Colombia, Cervical Intraepithelial Neoplasia

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
2661 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HPV test
Arm Type
Experimental
Arm Description
Women with ASC-US cytology are HPV tested and those HPV positive are refer to Colposcopy
Arm Title
COLPOSCOPY
Arm Type
Active Comparator
Arm Description
Women with ASC-US cytology are immediately refer to colposcopy
Arm Title
CYTOLOGY
Arm Type
Active Comparator
Arm Description
Women 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
Intervention Type
Device
Intervention Name(s)
HPV test
Other Intervention Name(s)
Human Papillomavirus test, DNA HPV test, High risk HPV test
Intervention Description
QIAGEN - The Digene HPV test®
Intervention Type
Procedure
Intervention Name(s)
COLPOSCOPY
Intervention Description
Colposcopy routine health services
Intervention Type
Device
Intervention Name(s)
cytology
Other Intervention Name(s)
Pap smear, Papanicolaou test, cervical cytology
Intervention Description
Cytology routine health services
Primary Outcome Measure Information:
Title
Cumulative Number of Participants Diagnosed by the Community Pathologist With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Community-based CIN2+"
Description
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.
Time Frame
Two years since the enrolment to the exit visit (inclusive)
Secondary Outcome Measure Information:
Title
Cumulative Number of Participants Diagnosed by a Panel of External Experts With Cervical Intraepithelial Neoplasia Grade 2 or Higher (CIN2+): "Reviewed CIN2+"
Description
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.
Time Frame
Two years since the enrolment to the exit visit (inclusive)
Title
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+"
Description
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.
Time Frame
Exit visit (two years after the enrolment)
Title
Number of Clinical Records (Cytologies, Colposcopies, and Histologies): "Health Care Utilization"
Description
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.
Time Frame
Two years since the enrolment to before the exit visit (i.e., excluding clinical records collected at the exit visit)
Title
Self-esteem
Description
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.
Time Frame
Two years between the enrolment and the exit visit
Title
Trait Anxiety
Description
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.
Time Frame
Two years between the enrolment and the exit visit
Title
State Anxiety
Description
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.
Time Frame
Two years between the enrolment and the exit visit
Title
Concerns About Fertility, Cancer, and Gynecological Health
Description
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.
Time Frame
Two years between the enrolment and the exit visit

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ASC-US cytology, living in metropolitan area of Medellin Exclusion Criteria: Previous abnormal cytology
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gloria I Sanchez, MSc, PhD
Organizational Affiliation
Universidad de Antioquia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Armando Baena, MSc, PhD
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria C Agudelo, MD
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Alejandra Botero, MSc
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Victor Florez, MSc
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Calatina Villa, BSc
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Astrid Bedoya, MSc
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Guadalupe Posada, MD, Esp
Organizational Affiliation
DINAMICA IPS
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Carlos A Buitrago, MD, Esp
Organizational Affiliation
EPS COMFENALCO
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Juan C Ochoa, MD, Esp
Organizational Affiliation
EPS COMFAMA
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Luis J Gomez, MD, Esp
Organizational Affiliation
DINAMICA IPS
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tatiana Ramirez, BSc
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maribel Almonte, MSc, PhD
Organizational Affiliation
International Agency for Research on Cancer (IARC)
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rolando Herrero, MSc, PhD
Organizational Affiliation
International Agency for Research on Cancer (IARC)
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Peter Sasieni, MSc, PhD
Organizational Affiliation
Centre for Cancer Prevention, Queen Mary University of London
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Yessid Álvarez, Student
Organizational Affiliation
Universidad de Antioquia
Official's Role
Study Chair
Facility Information:
Facility Name
Universidad de Antioquia
City
Medellin
State/Province
Antioquia
Country
Colombia

12. IPD Sharing Statement

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Citation
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
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PubMed Identifier
32617889
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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.
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PubMed Identifier
32049551
Citation
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.
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Optimal Strategy for the Management of ASCUS Cytology in Health Care Services of Medellin, Colombia

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