Evidence map›Paper›PMID 36946291›Full record

ArticleJournal of the National Cancer Institute2023

Risk prediction of hepatitis B or C or HIV among newly diagnosed cancer patients.

Joseph M Unger, Cathee Till, Jessica P Hwang, Kathryn B Arnold, Michael Leblanc, Dawn L Hershman, Scott D Ramsey

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Journal of the National Cancer Institute, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 1 country.

Joseph M UngerSWOG Statistics and Data Management Center, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-5191-0317
Cathee TillSWOG Statistics and Data Management Center, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-6801-8333
Jessica P HwangThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Kathryn B ArnoldSWOG Statistics and Data Management Center, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Michael LeblancSWOG Statistics and Data Management Center, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Dawn L HershmanColumbia University, New York, NY, USA.
Scott D RamseyFred Hutchinson Cancer Center, Seattle, WA, USA.
Fred Hutch Cancer Center · USColumbia University · USThe University of Texas MD Anderson Cancer Center · US

Funding

SWOG NCORP Research BaseUG1CA189974 · NCI · THE HOPE FOUNDATION · PI CHARLES D. BLANKE, DAWN HERSHMAN · 2014 to 2026
$80.6M
NCI NIH HHS UG1 CA189974NCI NIH HHS UG1CA189974
6 · The paper itself

Abstract

backgroundScreening for viral infection in cancer patients is inconsistent. A mechanism to readily identify cancer patients at increased risk of existing or prior viral infection could enhance screening efforts while reducing costs.

methodsWe identified factors associated with increased risk of past or chronic hepatitis virus B, hepatitis virus C, or HIV infection before initiation of systemic cancer therapy. Data were from a multicenter prospective cohort study of 3051 patients with newly diagnosed cancer (SWOG-S1204) enrolled between 2013 and 2017. Patients completed a survey with questions pertaining to personal history and behavioral, socioeconomic, and demographic risk factors for viral hepatitis or HIV. We derived a risk model to predict the presence of viral infection in a random set of 60% of participants using best subset selection. The derived model was validated in the remaining 40% of participants. Logistic regression was used.

resultsA model with 7 risk factors was identified, and a risk score with 4 levels was constructed. In the validation cohort, each increase in risk level was associated with a nearly threefold increased risk of viral positivity (odds ratio = 2.85, 95% confidence interval = 2.26 to 3.60, P < .001). Consistent findings were observed for individual viruses. Participants in the highest risk group (with >3 risk factors), comprised of 13.4% of participants, were 18 times more likely to be viral positive compared with participants with no risk factors (odds ratio = 18.18, 95% confidence interval = 8.00 to 41.3, P < .001).

conclusionsA risk-stratified screening approach using a limited set of questions could serve as an effective strategy to streamline screening for individuals at increased risk of viral infection.

Indexed as

Hepatitis BHIV InfectionsNeoplasmsHumansProspective StudiesRisk Factors

Identifiers

PMID36946291
PMCPMC10248838
OpenAlexW4330334944

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.