Evidence map›Paper›PMID 32314052›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2021

Strategies to identify hepatitis C virus infection in patients receiving anticancer therapy: a cross-sectional study.

Harrys A Torres, Anna S Lok, Maria E Suarez-Almazor, Carla L Warneke, Ahmed Kaseb, Ethan Miller, Erich M Sturgis, Jessica T Foreman, Georgios Angelidakis, Sairah Ahmed and 4 more

Open access · greenAbstract read
In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 95% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

14 authors at 2 institutions in 1 country.

Harrys A TorresDepartment of Infectious Diseases, Infection Control & Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Anna S LokDivision of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI, USA.
Maria E Suarez-AlmazorDepartment of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Carla L WarnekeDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ahmed KasebDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ethan MillerDepartment of Gastroenterology, Hepatology & Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Erich M SturgisDepartment of Head & Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jessica T ForemanDepartment of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Georgios AngelidakisDepartment of Infectious Diseases, Infection Control & Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sairah AhmedDepartment of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Alessandra FerrajoliDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Felipe SamaniegoDepartment of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ernest T HawkDivision of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jessica P HwangDepartment of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. jphwang@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of Michigan–Ann Arbor · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
HBV reactivation among cancer patients receiving chemotherapyK07CA132955 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HWANG, JESSICA PARK · 2010 to 2014
$702k
Widespread vs Selective Screening for Hepatitis B Infection Prior to ChemotherapyR21CA167202 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HWANG, JESSICA PARK · 2013 to 2014
$372k
MD Anderson Cancer Center Clinical Trials Support Resource P30CA016672NCI NIH HHS K07 CA132955NCI NIH HHS K07CA132955NCI NIH HHS P30 CA016672NCI NIH HHS R21 CA167202NCI NIH HHS R21CA167202
6 · The paper itself

Abstract

backgroundOptimal hepatitis C virus (HCV) screening strategies for cancer patients have not been established. We compared the performance of selective HCV screening strategies.

methodsWe surveyed patients presenting for first systemic anticancer therapy during 2013-2014 for HCV risk factors. We estimated the prevalence of positivity for HCV antibody (anti-HCV) and examined factors associated with anti-HCV status using Fisher's exact test or Student's t test. Sensitivity was calculated for screening patients born during 1945-1965, patients with ≥ 1 other risk factor, or both cohorts ("combined screening").

resultsWe enrolled 2122 participants. Median age was 59 years (range, 18-91); 1138 participants were women. Race/ethnicity distribution was white non-Hispanic, 76% (n = 1616); Hispanic, 11% (n = 233); black non-Hispanic, 8% (n = 160); Asian, 4% (n = 78); and other, 2% (n = 35). Primary cancer distribution was non-liver solid tumor, 78% (n = 1664); hematologic cancer, 20% (n = 422); and liver cancer, 1% (n = 28). Prevalence of anti-HCV was 1.93% (95% CI, 1.39%-2.61%). Over 28% of patients with detectable HCV RNA were unaware of infection. Factors significantly associated with anti-HCV positivity included less than a bachelor's degree, birth in 1945-1965, chronic liver disease, injection drug use, and blood transfusion or organ transplant before 1992. A total of 1315 participants (62%), including 39 of 41 with anti-HCV, reported ≥ 1 risk factor. Sensitivity was 80% (95% CI, 65-91%) for birth-cohort-based, 68% (95% CI, 52-82%) for other-risk-factor-based, and 95% (95% 83-99%) for combined screening.

conclusionCombined screening still missed 5% of patients with anti-HCV. These findings favor universal HCV screening to identify all HCV-infected cancer patients.

Indexed as

AdolescentAdultAgedAged, 80 and overBlack or African AmericanCross-Sectional StudiesFemaleHepacivirusHepatitis CHepatitis C AntibodiesHispanic or LatinoHumansLiver NeoplasmsMaleMass ScreeningMiddle AgedHepatitis C AntibodiesRNA, ViralDrug therapyHepatitis C virusNeoplasmsVirus activation

Identifiers

PMID32314052
PMCPMC9706509
OpenAlexW3016342026

What OpenQuestion holds

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Registered trials

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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.