Evidence map›Paper›PMID 32510043›Full record

ArticleEClinicalMedicine2020

A study of type-specific HPV natural history and implications for contemporary cervical cancer screening programs.

Maria Demarco, Noorie Hyun, Olivia Carter-Pokras, Tina R Raine-Bennett, Li Cheung, Xiaojian Chen, Anne Hammer, Nicole Campos, Walter Kinney, Julia C Gage and 13 more

Open access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 3 pooled it
16.6field-weighted citation impact, top 1% of its field
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

118 citing papers in PubMed, 3 syntheses or guidelines pooled it, 210 citations in OpenAlex.

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

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 10 institutions in 3 countries.

Maria DemarcoDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Noorie HyunDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Olivia Carter-PokrasUniversity of Maryland School of Public Health, College Park, MD, United States.
Tina R Raine-BennettDivision of Research, Kaiser Permanente Northern California, Oakland, CA, United States.
Li CheungDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Xiaojian ChenDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Anne HammerDepartment of Obstetrics and Gynecology, Aarhus University Hospital, Denmark.
Nicole CamposCenter for Health Decision Science, Department of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
Walter KinneyRegional Laboratory, Kaiser Permanente Northern California, Berkeley, CA, United States.
Julia C GageDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Brian BefanoInformation Management Services Inc., Calverton, MD, United States.
Rebecca B PerkinsDepartment of Obstetrics and Gynecology, Boston Medical Center/Boston University School of Medicine, Boston, MA, United States.
Xin HeUniversity of Maryland School of Public Health, College Park, MD, United States.
Cher DallalUniversity of Maryland School of Public Health, College Park, MD, United States.
Jie ChenUniversity of Maryland School of Public Health, College Park, MD, United States.
Nancy PoitrasRegional Laboratory, Kaiser Permanente Northern California, Berkeley, CA, United States.
Marie-Helene MayrandDepartment of Obstetrics and Gynecology, Université de Montréal and Centre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
Francois CoutleeDepartment of Microbiology, Université de Montréal and CRCHUM, Montreal, Canada.
Robert D BurkAlbert Einstein College of Medicine, Bronx, NY, United States.
Thomas LoreyRegional Laboratory, Kaiser Permanente Northern California, Berkeley, CA, United States.
Philip E CastleAlbert Einstein College of Medicine, Bronx, NY, United States.
Nicolas WentzensenDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Mark SchiffmanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, United States.
Division of Cancer Epidemiology and GeneticsKaiser Permanente · USUniversity of Maryland, College Park · USAlbert Einstein College of Medicine · USNational Cancer Institute · USAarhus University · DKBoston Medical Center · USCentre Hospitalier de l’Université de Montréal · CAInformation Management Services · USUniversité de Montréal · CA

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
Human Papillomavirus (HPV) Natural History, Genomics and Risk AssessmentZIACP010206 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SCHIFFMAN, MARK · 2010 to 2025
$17.1M
PERSISTENT HUMAN PAPILLOMAVIRUS IN WOMEN AT RISK FOR CERVIX CANCERU01CA078527 · NCI · YESHIVA UNIVERSITY · PI BURK, ROBERT D · 2003 to 2018
$8.6M
Investigations Into The Molecular Pathogenesis Of Cervical Glandular NeoplasiasU01CA238592 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BURK, ROBERT D, STRICKLER, HOWARD D · 2020 to 2024
$2.8M
PERSISTENT HPV IN WOMEN AT RISK FOR CERVIX CANCERR01CA078527 · NCI · YESHIVA UNIVERSITY · PI BURK, ROBERT D. · 1998 to 2002
$1.5M
NCI NIH HHS P30 CA013330NCI NIH HHS R01 CA078527NCI NIH HHS U01 CA078527NCI NIH HHS U01 CA238592
6 · The paper itself

Abstract

backgroundHPV testing is replacing cytology for cervical cancer screening because of greater sensitivity and superior reassurance following negative tests for the dozen HPV genotypes that cause cervical cancer. Management of women testing positive is unresolved. The need for identification of individual HPV genotypes for clinical use is debated. Also, it is unclear how long to observe persistent infections when precancer is not initially found.

methodsIn the longitudinal NCI-Kaiser Permanente Northern California Persistence and Progression (PaP) Study, we observed the clinical outcomes (clearance, progression to CIN3+, or persistence without progression) of 11,573 HPV-positive women aged 30-65 yielding 14,158 type-specific infections.

findingsRisks of CIN3+ progression differed substantially by type, with HPV16 conveying uniquely elevated risk (26% of infections with seven-year CIN3+ risk of 22%). The other carcinogenic HPV types fell into 3 distinct seven-year CIN3+ risk groups: HPV18, 45 (13% of infections, risks >5%, with known elevated cancer risk); HPV31, 33, 35, 52, 58 (39%, risks >5%); and HPV39, 51, 56, 59, 68 (23%, risks <5%). In the absence of progression, HPV clearance rates were similar by type, with 80% of infections no longer detected within three years; persistence to seven years without progression was uncommon. The predictive value of abnormal cytology was most evident for prevalent CIN3+, but less evident in follow-up. A woman's age did not modify risk; rather it was the duration of persistence that was important.

interpretationHPV type and persistence are the major predictors of progression to CIN3+; at a minimum, distinguishing HPV16 is clinically important. Dividing the other HPV types into three risk-groups is worth considering.

Indexed as

AGC, Atypical glandular cellsAIS, Adenocarcinoma in-situASC-H+, Atypical squamous cells - cannot exclude HSILASC-US, Atypical squamous cells of undetermined significanceBD, Becton DickinsonCIN, Cervical intraepithelial neoplasiaHC2, Hybrid Capture 2HPV genotypeHPV, human papillomavirusHPV outcome, ClearanceKPNC, Kaiser Permanente Northern CaliforniaLSIL, Low-grade squamous intraepithelial lesionNCI, National Cancer InstituteNILM, Negative for intraepithelial lesion or malignancyPaP, Persistence and ProgressionPCR, Polymerase chain reactionPersistenceProgressionSTM, Specimen transport medium

Identifiers

PMID32510043
PMCPMC7264956
OpenAlexW3020439257

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.