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Performance of CADM1, MAL and miR124-2 methylation as triage markers for early detection of cervical cancer in self-collected and clinician-collected samples: an exploratory observational study in Papua New Guinea.
Molano, Monica; Machalek, Dorothy A; Tan, Grace; Garland, Suzanne; Balgovind, Prisha; Haqshenas, Gholamreza; Munnull, Gloria; Phillips, Samuel; Badman, Steven G; Bolnga, John; Cornall, Alyssa Marie; Gabuzzi, Josephine; Kombati, Zure; Brotherton, Julia; Saville, Marion; Hawkes, David; Kaldor, John; Toliman, Pamela Josephine; Vallely, Andrew John; Murray, Gerald L.
Afiliação
  • Molano M; Centre for Women's Infectious Diseases, The Royal Women's Hospital, Parkville, Victoria, Australia monica.molanoluque@thewomens.org.au.
  • Machalek DA; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Tan G; Centre for Women's Infectious Diseases, The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Garland S; Kirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
  • Balgovind P; Australian Centre for the Prevention of Cervical Cancer, Melbourne, Victoria, Australia.
  • Haqshenas G; The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Munnull G; Department of Obstetrics, Gynaecology and Newborn Health, The University of Melbourne, Melbourne, Victoria, Australia.
  • Phillips S; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Badman SG; The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Bolnga J; The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Cornall AM; Department of Obstetrics, Gynaecology and Newborn Health, The University of Melbourne, Melbourne, Victoria, Australia.
  • Gabuzzi J; Papua New Guinea Institute of Medical Research, Goroka, Papua New Guinea.
  • Kombati Z; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Brotherton J; The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Saville M; Kirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
  • Hawkes D; Papua New Guinea Institute of Medical Research, Goroka, Papua New Guinea.
  • Kaldor J; Obstetrics and Gynaecology, Modilon General Hospital, Madang, Papua New Guinea.
  • Toliman PJ; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Vallely AJ; The Royal Women's Hospital, Parkville, Victoria, Australia.
  • Murray GL; Papua New Guinea Institute of Medical Research, Goroka, Papua New Guinea.
BMJ Open ; 14(6): e081282, 2024 Jun 19.
Article em En | MEDLINE | ID: mdl-38904134
ABSTRACT

OBJECTIVE:

WHO recommends human papillomavirus (HPV) testing for cervical screening, with triage of high-risk HPV (hrHPV) positive women. However, there are limitations to effective triage for low-resource, high-burden settings, such as Papua New Guinea. In this exploratory study, we assessed the performance of host methylation as triage tools for predicting high-grade squamous intraepithelial lesions (HSIL) in self-collected and clinician-collected samples.

DESIGN:

Exploratory observational study.

SETTING:

Provincial hospital, same-day cervical screen-and-treat trial, Papua New Guinea.

PARTICIPANTS:

44 hrHPV+women, with paired self/clinician-collected samples (4 squamous cell carcinomas (SCC), 19 HSIL, 4 low-grade squamous intraepithelial lesions, 17 normal). PRIMARY AND SECONDARY OUTCOME

MEASURES:

Methylation levels of CADM1, MAL and miR124-2 analysed by methylation-specific PCRs against the clinical endpoint of HSIL or SCC (HSIL+) measured using liquid-based-cytology/p16-Ki67 stain.

RESULTS:

In clinician-collected samples, MAL and miR124-2 methylation levels were significantly higher with increasing grade of disease (p=0.0046 and p<0.0015, respectively). miR124-2 was the best predictor of HSIL (area under the curve, AUC 0.819) while MAL of SCC (AUC 0.856). In self-collected samples, MAL best predicted HSIL (AUC 0.595) while miR124-2 SCC (AUC 0.812). Combined miR124-2/MAL methylation yielded sensitivity and specificity for HSIL+ of 90.5% (95% CI 69.6% to 98.8%) and 70% (95% CI 45.7% to 88.1%), respectively, in clinician-collected samples, and 81.8% (95% CI 59.7% to 94.8%) and 47.6% (95% CI 25.7% to 70.2%), respectively, in self-collected samples. miR124-2/MAL plus HPV16/HPV18 improved sensitivity for HSIL+ (95.2%, 95% CI 76.2% to 99.9%) but decreased specificity (55.0%, 95% CI 31.5% to 76.9%).

CONCLUSION:

miR124-2/MAL methylation is a potential triage strategy for the detection of HSIL/SCC in low-income and middle-income country.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo do Útero / Triagem / Metilação de DNA / Infecções por Papillomavirus / MicroRNAs / Detecção Precoce de Câncer / Proteínas Proteolipídicas Associadas a Linfócitos e Mielina / Molécula 1 de Adesão Celular Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo do Útero / Triagem / Metilação de DNA / Infecções por Papillomavirus / MicroRNAs / Detecção Precoce de Câncer / Proteínas Proteolipídicas Associadas a Linfócitos e Mielina / Molécula 1 de Adesão Celular Idioma: En Ano de publicação: 2024 Tipo de documento: Article