Evidence map›Paper›PMID 22810146›Full record

Trial reportCancer causes & control : CCC2012

Prospective study of cytomegalovirus serostatus and prostate cancer risk in the Prostate Cancer Prevention Trial.

Siobhan Sutcliffe, Cathee Till, Charlotte A Gaydos, Frank J Jenkins, Phyllis J Goodman, Ashraful M Hoque, Ann W Hsing, Ian M Thompson, Jonathan M Zenilman, William G Nelson and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Cancer causes & control : CCC, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
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

12 authors at 7 institutions in 1 country.

Siobhan SutcliffeDivision of Public Health Sciences and the Alvin J. Siteman Cancer Center, Department of Surgery, Washington University School of Medicine, 660 S. Euclid Ave., Rm. 5026, Box 8100, St. Louis, MO 63110, USA. sutcliffes@wudosis.wustl.edu
Cathee Till
Charlotte A Gaydos
Frank J Jenkins
Phyllis J Goodman
Ashraful M Hoque
Ann W Hsing
Ian M Thompson
Jonathan M Zenilman
William G Nelson
Angelo M De Marzo
Elizabeth A Platz
Johns Hopkins University · USFred Hutch Cancer Center · USAlvin J. Siteman Cancer CenterCancer Prevention Institute of California · USThe University of Texas Health Science Center at San Antonio · USThe University of Texas MD Anderson Cancer Center · USUniversity of Pittsburgh · US

Funding

SWOG Foreign AccrualsU10CA037429 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BLANKE, CHARLES D., MEYSKENS, FRANK L. · 1985 to 2014
$205.2M
VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Oxidative Damage and DNA Repair in the PCPTP01CA108964 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI THOMPSON, IAN M · 2005 to 2009
$13.6M
NCI NIH HHS P01 CA108964NCI NIH HHS P30 CA023100NCI NIH HHS P30 CA054174NCI NIH HHS U01 CA37429NCI NIH HHS U10 CA037429
6 · The paper itself

Abstract

purposeTo investigate serologic evidence of infection by cytomegalovirus (CMV), a herpesvirus with known oncogenic potential that has been detected in malignant prostate tissue, in relation to prostate cancer (PCa) risk in a large case-control study nested in the Prostate Cancer Prevention Trial (PCPT).

methodsCases were men with a confirmed diagnosis of PCa after visit 2 (n = 614), and controls were men not diagnosed with PCa during the trial who also had a negative end-of-study biopsy (n = 616). Controls were frequency-matched to cases by age, treatment arm, and family history of PCa. Sera from visit 2 were tested for CMV IgG antibodies.

resultsNo association was observed between CMV serostatus and PCa risk (adjusted CMV seroprevalence = 67.9 % for cases and 65.2 % for controls, odds ratio = 1.13, 95 % CI 0.89-1.45).

conclusionsConsidering our null findings in the context of the full CMV literature, CMV infection, as measured by serostatus, does not appear to increase PCa risk.

Indexed as

5-alpha Reductase InhibitorsAgedAged, 80 and overCase-Control StudiesCytomegalovirusCytomegalovirus InfectionsFinasterideHumansMaleMiddle AgedProspective StudiesProstatic NeoplasmsRisk FactorsSeroepidemiologic Studies5-alpha Reductase InhibitorsFinasteride

Identifiers

PMID22810146
PMCPMC3433040
OpenAlexW2010163263

What OpenQuestion holds

Textmetadata
LicenceTDM
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.