Primary HPV-DNA screening in women under 30 years of age: health technology assessment

Authors

DOI:

https://doi.org/10.18597/rcog.3866

Keywords:

Biomedical technology assessment, cost-benefit analysis, early cancer detection, uterine cervix neoplasms

Abstract

Background
Primary screening with Human Papilloma Virus (HPV) testing was introduced in Colombia in 2014 for individuals between 30 and 65 years of age. When the result is positive, cytology triage is performed for colposcopy referral. The convenience of initiating HPV-DNA testing for screening at 25 years of age is currently a subject of discussion. Therefore, the objective of this health technology assessment (HTA) is to analyze the available evidence regarding safety, efficacy, cost-effectiveness, values and preferences, ethical dilemmas and considerations pertaining to the implementation of the HPV-DNA test as a cervical screening strategy in women under 30 years of age in the Colombian context.

Domains to be assessed
Clinical efficacy and safety
1. Cumulative rate of cervical intraepithelial neoplasia (CIN) grade 2 or high-er after 2 screening rounds.
2. Cumulative rates of invasive cancer of the uterine cervix after 2 screening rounds.
3. Safety: referral to colposcopy

Cost-effectiveness
Cost-effectiveness for Colombia.

Other domains considered
Ethical considerations associated with cervical screening in women under 30 years of age. Organizational and individual considerations. Barriers and facilitators pertaining to the implementation of cervical screening in women under 30 years of age in the Colombian context.

Methods

Clinical efficacy and safety assessment
A systematic literature search of systematic reviews and clinical trials was conducted in MEDLINE, Embase and CENTRAL. The body of evidence was rated using the GRADE approach. An interdisciplinary team was then convened to create a working group to review the retrieved evidence. This led to the discussion and construction of the conclusions following the guidelines of a formal consensus in accordance with the RAND/UCLA methodology.

Economic study
Systematic literature research of studies that had assessed cost-effectiveness for Colombia.

Results
Out of the 7,659 references retrieved, 8 studies were included.

Clinical outcomes
An integrative analysis of 5 randomized clinical trials that met the inclusion critera was performed. Compared with cytology, primary HPV-DNA testing in women under 30 years of age could be associated with a lower frequency of CIN+2 lesions during the first screening round (RR: 1.57; CI: 1.20 to 2.04; low evidence certainty), and a lower incidence of CIN+2 (RR: 0.67; CI: 0.48 to 0.92; low evidence certainty). Moreover, it is associated with a lower frequency of invasive carcinoma at the end of follow-up (RR: 0.19; CI: 0.07 to 0.53; high evidence certainty).

Economic results
From the financial point of view, the use of HPVDNA testing plus cytology-based triage starting at 25 years of age is perhaps the most cost-effective option for Colombia (incremental cost-effectiveness ratio, COP 8,820,980 in 2013).

Other implications
Two studies suggest that barriers to implementation attributable to intermediation, public unrest and geographic considerations could be overcome with the use of new screening technologies or strategies. It is important to consider administration and service provision alternatives in order to overcome some acceptability and access barriers. Any cervical screening program must take into consideration ethical principles of nonmaleficence, beneficence, autonomy and equity. Future studies should focus on analyzing new screening techniques with emphasis on the population under 30 years of age.

Conclusions
The use of HPV-DNA testing as a screening strategy in women under 30 years of age is a potentially efficacious and cost-effective intervention for Colombia. Future studies should focus on analyzing new screening technologies, with emphasis on the population under 30 years of age.

Author Biographies

Carmen Doris Garzón-Olivares, Universidad Nacional de Colombia, Bogotá (Colombia).

Profesora Asociada, Departamento de Obstetricia y Ginecología, Universidad Nacional de Colombia, Bogotá (Colombia).

Carlos Fernando Grillo-Ardila, Instituto Nacional de Cancerología, Bogotá (Colombia).

Profesor Asistente, Departamento de Obstetricia y Ginecología, Universidad Nacional de Colombia. Grupo de investigación clínica y epidemiológica del Cáncer, Instituto Nacional de Cancerología, Bogotá (Colombia).

Jairo Amaya-Guio, Universidad Nacional de Colombia, Bogotá (Colombia).

Profesor Titular, Departamento de Obstetricia y Ginecología, Universidad Nacional de Colombia, Bogotá (Colombia).

Maria Teresa Vallejo-Ortega, Instituto Nacional de Cancerología, Bogotá (Colombia).

Grupo de investigación clínica y epidemiológica del Cáncer, Instituto Nacional de Cancerología, Bogotá (Colombia).

Luz Amparo Diaz-Cruz, Universidad Nacional de Colombia, Bogotá (Colombia).

Profesora Asociada, Departamento de Obstetricia y Ginecología, Universidad Nacional de Colombia, Bogotá (Colombia).

Carolina Fernández-Motta, Universidad Surcolombiana, Neiva (Huila).

Universidad Surcolombiana, Neiva (Huila).

Alejandra del Pilar Gomez-Motta, Universidad Surcolombiana, Neiva (Huila).

Universidad Surcolombiana, Neiva (Huila).

Alina Tatiana Barrera, Universidad Surcolombiana, Neiva (Huila).

Universidad Surcolombiana, Neiva (Huila).

Lina María Trujillo-Sánchez, Instituto Nacional de Cancerología, Bogotá (Colombia).

Subdirectora General de Atención Médica y Docencia. Instituto Nacional de Cancerología, Bogotá (Colombia).

Carlos Humberto Pérez-Moreno, Federación Internacional de Patología del Tracto Genital Inferior y Colposcopia, Bogotá (Colombia).

Presidente Federación Internacional de Patología del Tracto Genital Inferior y Colposcopia, Bogotá (Colombia).

Luis Jairo Bonilla-Osma, Fundación Universitaria de Ciencias de las Salud, Bogotá (Colombia).

Profesor Fundación Universitaria de Ciencias de las Salud, Bogotá (Colombia).

Robinson Fernández-Mercado, Asociación Colombiana de Ginecólogos Oncólogos, Barranquilla (Colombia).

Profesor Universidad Libre de Barranquilla. Representante de Asociación Colombiana de Ginecólogos Oncólogos, Barranquilla (Colombia).

Néstor Augusto Giraldo-Méndez, Subred Integrada de servicios de Salud Norte-Bogotá, Bogotá (Colombia).

Coordinador Ginecología de Subred Integrada de servicios de Salud Norte-Bogotá, Bogotá (Colombia).

Jorge Eduardo Caro-Caro, Subred Integrada de servicios de Salud Centro-Oriente-Bogotá, Bogotá (Colombia).

Coordinador Ginecología de Subred Integrada de servicios de Salud Centro-Oriente-Bogotá, Bogotá (Colombia).

Amparo Leonor Ramírez-Corredor, Subred Integrada de Servicios de Salud Sur, Bogotá (Colombia).

Coordinadora Ginecología de Subred Integrada de Servicios de Salud Sur, Bogotá (Colombia).

Dayanne Milecsy Rodríguez-Hernández, Universidad Nacional de Colombia, Bogotá (Colombia).

Universidad Nacional de Colombia, Bogotá (Colombia).

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How to Cite

1.
Garzón-Olivares CD, Grillo-Ardila CF, Amaya-Guio J, Vallejo-Ortega MT, Diaz-Cruz LA, Fernández-Motta C, et al. Primary HPV-DNA screening in women under 30 years of age: health technology assessment. Rev. colomb. obstet. ginecol. [Internet]. 2022 Jun. 30 [cited 2024 May 17];73(2):203-22. Available from: https://revista.fecolsog.org/index.php/rcog/article/view/3866

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Published

2022-06-30

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