Evidence map›Paper›PMID 19638649›Full record

ArticleBMJ (Clinical research ed.)2009

Short term persistence of human papillomavirus and risk of cervical precancer and cancer: population based cohort study.

Philip E Castle, Ana Cecilia Rodríguez, Robert D Burk, Rolando Herrero, Sholom Wacholder, Mario Alfaro, Jorge Morales, Diego Guillen, Mark E Sherman, Diane Solomon and 2 more

Abstract read
In one paragraph

Article in BMJ (Clinical research ed.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 6 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

89 citing papers in PubMed, 6 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Guideline
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Human papillomavirus (HPV) genotypes in women with cervical precancer and cancer at Kaiser Permanente Northern California.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2011
    Trial
  13. Comparison of measurements of human papillomavirus persistence for postcolposcopic surveillance for cervical precancerous lesions.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2010
    Trial
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

29 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Philip E CastleDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD 20892, USA. castlep@mail.nih.gov
Ana Cecilia Rodríguez
Robert D Burk
Rolando Herrero
Sholom Wacholder
Mario Alfaro
Jorge Morales
Diego Guillen
Mark E Sherman
Diane Solomon
Mark Schiffman
Proyecto Epidemiológico Guanacaste (PEG) Group

Funding

Human papillomavirus (HPV) infection and cervical and anal cancersZIACP010124 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI WENTZENSEN, NICOLAS · 2009 to 2025
$17.3M
PERSISTENT HUMAN PAPILLOMAVIRUS IN WOMEN AT RISK FOR CERVIX CANCERU01CA078527 · NCI · YESHIVA UNIVERSITY · PI BURK, ROBERT D · 2003 to 2018
$8.6M
PERSISTENT HPV IN WOMEN AT RISK FOR CERVIX CANCERR01CA078527 · NCI · YESHIVA UNIVERSITY · PI BURK, ROBERT D. · 1998 to 2002
$1.5M
GUANACASTE PROJECT--A POPULATION BASED NATURAL HISTN01CP081023 · CP · FUNDACION COSTARRICENSE PARA LA DOCENCIA · PI BRATTI, CONCEPCION C · 1998 to 2000
$1.4M
POPULATION-BASED NATURAL HISTORY OF CERVICAL NEOPLASIAN01CP021081 · CP · FUNDACION COSTARRICENSE PARA LA DOCENCIA · PI PACHECO, MARIO · 1992 to 1993
–
POPULATION BASED NATURAL HISTORY OF CERVICAL NEOPLASIAN01CP050535 · CP · FUNDACION COSTARRICENSE PARA LA DOCENCIA · PI BRATTI, CONCEPCION C · 1995 to 1998
–
POPULATION-BASED NATURAL HISTORY OF CERVICAL NEOPLASIAN01CP040542 · CP · FUNDACION COSTARRICENSE PARA LA DOCENCIA · PI BRATTI, CONCEPCION · 1994 to 1994
–
POPULATION-BASED NATURAL HISTORY OF CERVICAL NEOPLASIAN01CP033061 · CP · FUNDACION COSTARRICENSE PARA LA DOCENCIA · PI PACHECO, MARIO · 1993 to 1994
–
Intramural NIH HHSNCI NIH HHS CA78527NCI NIH HHS N01-CP-21081NCI NIH HHS N01-CP-33061NCI NIH HHS N01-CP-40542NCI NIH HHS N01-CP-50535NCI NIH HHS N01-CP-81023NCI NIH HHS R01 CA078527NCI NIH HHS U01 CA078527
6 · The paper itself

Abstract

objectiveTo evaluate the cumulative incidence of cervical intraepithelial neoplasia II or worse (grade II+) or cervical intraepithelial neoplasia grade III+ after short term persistence of prevalently detected carcinogenic human papillomavirus (HPV).

designPopulation based cohort study.

settingGuanacaste, Costa Rica.

participants2282 sexually active women actively followed after enrolment.

main outcome measuresPrimary end points: three year and five year cumulative incidence of histologically confirmed cervical intraepithelial neoplasia grade II+ (n=70). Cervical specimens collected at each visit tested for more than 40 HPV genotypes. HPV 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68, 73, and 82 were considered the primary carcinogenic genotypes.

resultsWomen who tested positive for a carcinogenic HPV at enrolment and after about one year (9-21 months) (positive/positive) had a three year cumulative incidence of cervical intraepithelial neoplasia grade II+ of 17.0% (95% confidence interval 12.1% to 22.0%). Those who tested negative/positive (3.4%, 0.1% to 6.8%), positive/negative (1.2%, -0.2% to 2.5%), and negative/negative (0.5%, 0.1% to 0.9%) were at a significantly lower risk. There was little difference in the cumulative incidence of cervical intraepithelial neoplasia grade II+ between testing positive twice for any carcinogenic HPV genotype (same genotype or different genotypes) v testing positive twice for the same carcinogenic genotype (17.0% v 21.3%, respectively). Short term persistence of HPV 16 strongly predicted cervical intraepithelial neoplasia grade II+, with a three year cumulative incidence of 40.8% (26.4% to 55.1%). Similar patterns were observed for the five year cumulative incidence of grade II+ and for three year and five year cumulative incidence of grade III+.

conclusionsShort term persistence of a prevalently detected carcinogenic HPV infection, especially HPV 16, strongly predicts a subsequent diagnosis of cervical intraepithelial neoplasia II+ over the next few years.

Indexed as

AdolescentAdultAgedAged, 80 and overCohort StudiesCosta RicaFemaleHumansIncidenceMiddle AgedPapillomaviridaePapillomavirus InfectionsPrecancerous ConditionsRisk FactorsUterine Cervical DysplasiaUterine Cervical Neoplasms

Identifiers

PMID19638649
PMCPMC2718087

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.