Evidence map›Paper›PMID 40561138›Full record

ArticlePloS one2025

Associations between genetic HPV 16 diversity and cervical cancer prognosis.

Patrícia Patury, Fabio B Russomano, Miguel Angelo Martins Moreira, Nádia R C Kappaun, Liz Maria de Almeida, Raquel B M Carvalho, Luís Felipe L Martins

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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Patrícia PaturyGynecologic Oncology Department, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.
Fabio B RussomanoDepartment of Clinical and Surgical Care of Women, National Institute of Women, Children and Adolescents Health Fernandes Figueira, Rio de Janeiro, Rio de Janeiro, Brazil.
Miguel Angelo Martins MoreiraTumoral Genetics and Virology Program, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0003-1437-7522
Nádia R C KappaunDepartment of Physiotherapy, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0002-9743-3392
Liz Maria de AlmeidaDivision of Surveillance and Situation Analysis, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.
Raquel B M CarvalhoDepartment of Physiotherapy, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.
Luís Felipe L MartinsDivision of Surveillance and Situation Analysis, Brazilian National Cancer Institute (INCA), Ministry of Health, Rio de Janeiro, Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCervical cancer (CC) arises as a result of chronic and persistent female infection by different oncogenic human papillomaviruses (HPV). The incidence of this disease is still high in developing countries, such as Brazil, where diagnosis is often made in advanced stages. HPV 16 is the most common Papillomavirus genotype in CC worldwide. Studies regarding the association of different HPV 16 lineages with overall and disease-free CC survival rates can contribute to further understanding the behavior of different HPV 16 lineages concerning the prognosis of CC cases.

objectiveTo assess the CC prognosis of patients treated in a Brazilian institution concerning HPV16 lineages.

methodsData were obtained from a prospective cohort of 334 patients with CC recruited between July 2011 and March 2014 and treated at the Brazilian National Cancer Institute (INCA), in Rio de Janeiro, Brazil. HPV 16 lineages were identified in tumor tissue samples. Genetic HPV 16 diversity comprised 218 cases of lineage A, 10 of lineage B, 10 of lineage C, and 96 of lineage D. In addition to HPV 16 lineages, age, histopathological type, staging, and treatment completion were evaluated as predictors of CC prognosis.

resultsThe median patient age was 48 years. The most common histopathological type was squamous cell carcinoma (82.3%), followed by adenocarcinoma. Locally advanced disease staging was the most frequently detected, represented by similar stage II and III percentages (36.2% and 37.7%), followed by initial stage I (19.2%) and stage IV (6.9%). Two hundred two patients completed CC treatment. Age, histological type, staging, and treatment completion were associated with a higher risk of death, which was not observed for the HPV 16 lineage variable. With regard to age, an increase in each year of life led to approximately a 1% increase in the risk of death. Other histopathological types (poorly differentiated carcinoma, adenosquamous, neuroendocrine, and sarcoma) were associated with a higher risk of death compared with adenocarcinoma. Patients diagnosed in advanced stages exhibited a higher risk of death, and those who did not complete treatment exhibited an over 2-fold increased risk of death.

conclusionThis study found no associations between HPV 16 lineages A, B, C, and D and CC prognosis.

Indexed as

Genetic VariationHuman papillomavirus 16Papillomavirus InfectionsUterine Cervical NeoplasmsAdultBrazilFemaleGenotypeHumansMiddle AgedNeoplasm StagingPrognosisProspective StudiesSurvival Rate

Identifiers

PMID40561138
PMCPMC12193069

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