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Longitudinal outcomes of high-risk human papillomavirus (HPV) infections as competing-risks events following cervical HPV test at baseline visit in the *NIS-LAMS** cohort

  • K. Syrjänen1,*,
  • I. Shabalova2
  • L. Sarian3
  • P. Naud4
  • A. Longatto-Filho5
  • S. Derchain3
  • V. Kozachenko2
  • S. Zakharchenko6
  • C. Roteli-Martins7
  • R. Nerovjna8
  • L. Kljukina9
  • S. Tatti10
  • M. Branovskaja11
  • M. Branca12
  • V. Grunjberga13
  • M. Eržen14
  • A. Juschenko13
  • L. Serpa Hammes4
  • J. Podistov15
  • S. Costa16
  • S. Syrjänen17
  • NIS Study Research Groups
  • LAMS Study Research Groups

1Department of Oncology & Radiotherapy, Turku University Hospital, Turku, Finland

2Russian Academy of Post-Graduate Medical Education, Moscow, Russia

3Universidade Estadual de Campinas, Campina, Brazil

4Hospital de Clinicas de Porto Alegre, and Department of Gynecology and Obstetrics, Federal University of Rio Grande do Sul, Porto Alegre, Brazil

5Laboratory of Medical Investigation (LIM14), Department of Pathology, Faculty of Medicine, São Paulo University, São Paulo University, São Paulo (Brazil) and Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal

6Novgorod Municipal Dermato-venereological Dispensary, Department of Gynaecology, Novgorod, Russia

7Hospital Leonor M de Barros, Sao Paulo, Brazil

8Novgorod Female Consultative Outpatient Hospital, Department of Gynaecology, Novgorod, Russia

9Research Institute of Oncology and Medical Radiology, Republican Centre of Clinical Cytology, Minsk, Belarus

10First Chair Gynecology Hospital de Clinicas, Buenos Aires, Argentina

11Minsk State Medical Institute, Department of Gynaecology and Obstetrics, Minsk, Belarus

12Unit of Cytopathology, National Centre of Epidemiology, Surveillance and Promotion of Health, National Institute of Health (ISS), Rome, Italy

13Latvian Cancer Centre, Department of Gynaecology, and Laboratory of Cytology, Riga, Latvia

14SIZE Diagnostic Center, Ljubljana, Slovenia

15N.N. Blokhin Cancer Research Centre of Russian Academy of Medical Sciences (RAMS), Moscow, Russia

16Department of Obstetrics and Gynecology, S. Orsola-Malpighi Hospital, Bologna, Italy

17Department of Oral Pathology, Institute of Dentistry, University of Turku, Finland

DOI: 10.12892/ejgo201204341 Vol.33,Issue 4,July 2012 pp.341-352

Published: 10 July 2012

*Corresponding Author(s): K. Syrjänen E-mail: kari.syrjanen@tyks.fi

Abstract

Background: The complex natural history of human papillomavirus (HPV) infections following a single HPV test can be modeled as competing-risks events (i.e., no-, transient- or persistent infection) in a longitudinal setting. The covariates associated with these compet ng events have not been previously assessed using competing-risks regression models. Objectives: To gain further insights in the outcomes of cervical HPV infections, we used univariate- and multivariate competing-risks regression models to assess the covariaies associated with these competing events. Study Design and Methods: Covariates associated with three competing outcomes (no-, transient- or persistent HR-HPV infection) were analysed in a sub-cohort of 1,865 women prospectively followed-up in the NIS (n = 3,187) and LAMS Study (n = 12,114). Results: In multivariate competing-risks models (with two other outcomes as competing events), permanently HR-HPV negative outcome was significantly predicted only by the clearance of ASCUS+Pap during FU, while three independent covariates predicted transient HR-HPV infections: i) number of recent (< 12 months) sexual partners (risk increased), ii) previous Pap screening history (protective), and history of previous CIN (increased risk). The two most powerful predictors of persistent HR-HPV infections were persistent ASCUS+Pap (risk increased), and previous Pap screening history (protective). In pair-wise comparisons, number of recent sexual partners and previous CIN history increase the probability of transient HR-HPV infection against the HR-HPV negative competing event, while previous Pap screening history is protective. Persistent ASCUS+Pap during FU and no previous Pap screening history are significantly associated with the persistent HR-HPV outcome (compared both with i) always negative, and ii) transient events), whereas multiparity is protective. Conclusions: Different covariates are associated with the three main outcomes of cervical HPV infections. The most significant covariates of each competing events are probably distinct enough to enable constructing of a risk-profile for each main outcome.

Keywords

HPV; Natural history; Outcomes; Competing events; Competing-risks regression model; Transient infection; Persistent infection; Prospective follow-up; NIS Cohort; LAMS Study

Cite and Share

K. Syrjänen,I. Shabalova,L. Sarian,P. Naud,A. Longatto-Filho,S. Derchain,V. Kozachenko,S. Zakharchenko,C. Roteli-Martins,R. Nerovjna,L. Kljukina,S. Tatti,M. Branovskaja,M. Branca,V. Grunjberga,M. Eržen,A. Juschenko,L. Serpa Hammes,J. Podistov,S. Costa,S. Syrjänen,NIS Study Research Groups,LAMS Study Research Groups. Longitudinal outcomes of high-risk human papillomavirus (HPV) infections as competing-risks events following cervical HPV test at baseline visit in the *NIS-LAMS** cohort. European Journal of Gynaecological Oncology. 2012. 33(4);341-352.

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