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


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 11 12 2019
accepted: 01 04 2020
pubmed: 22 4 2020
medline: 5 1 2021
entrez: 22 4 2020
Statut: ppublish

Résumé

Optimal hepatitis C virus (HCV) screening strategies for cancer patients have not been established. We compared the performance of selective HCV screening strategies. We 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"). We 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. Combined screening still missed 5% of patients with anti-HCV. These findings favor universal HCV screening to identify all HCV-infected cancer patients.

Sections du résumé

BACKGROUND BACKGROUND
Optimal hepatitis C virus (HCV) screening strategies for cancer patients have not been established. We compared the performance of selective HCV screening strategies.
METHODS METHODS
We 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").
RESULTS RESULTS
We 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.
CONCLUSION CONCLUSIONS
Combined screening still missed 5% of patients with anti-HCV. These findings favor universal HCV screening to identify all HCV-infected cancer patients.

Identifiants

pubmed: 32314052
doi: 10.1007/s00520-020-05456-3
pii: 10.1007/s00520-020-05456-3
pmc: PMC9706509
mid: NIHMS1799248
doi:

Substances chimiques

Hepatitis C Antibodies 0
RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

97-105

Subventions

Organisme : NCI NIH HHS
ID : K07 CA132955
Pays : United States
Organisme : NCI NIH HHS
ID : K07CA132955
Pays : United States
Organisme : MD Anderson Cancer Center Clinical Trials Support Resource
ID : P30CA016672
Organisme : NCI NIH HHS
ID : R21CA167202
Pays : United States

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Auteurs

Harrys A Torres (HA)

Department of Infectious Diseases, Infection Control & Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Gastroenterology, Hepatology & Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Anna S Lok (AS)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI, USA.

Maria E Suarez-Almazor (ME)

Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Carla L Warneke (CL)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Ahmed Kaseb (A)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Ethan Miller (E)

Department of Gastroenterology, Hepatology & Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Erich M Sturgis (EM)

Department of Head & Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Jessica T Foreman (JT)

Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Georgios Angelidakis (G)

Department of Infectious Diseases, Infection Control & Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Sairah Ahmed (S)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Alessandra Ferrajoli (A)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Felipe Samaniego (F)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Ernest T Hawk (ET)

Division of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Jessica P Hwang (JP)

Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. jphwang@mdanderson.org.

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