Cargando…
789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients
BACKGROUND: Patients with certain types of cancer are at increased risk for progression from latent tuberculosis infection (LTBI) to active tuberculosis (ATB) because of immunosuppression. The purpose of this study was to compare the utility of the two commonly used IGRAs, QuantiFERON-TB Gold(®) (QF...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254052/ http://dx.doi.org/10.1093/ofid/ofy210.796 |
_version_ | 1783373634855763968 |
---|---|
author | Kulkarni, Prathit Kmeid, Joumana Batista, Marjorie Chaer, Firas El Ariza-Heredia, Ella Graviss, Edward A Mulanovich, Victor E Chemaly, Roy F |
author_facet | Kulkarni, Prathit Kmeid, Joumana Batista, Marjorie Chaer, Firas El Ariza-Heredia, Ella Graviss, Edward A Mulanovich, Victor E Chemaly, Roy F |
author_sort | Kulkarni, Prathit |
collection | PubMed |
description | BACKGROUND: Patients with certain types of cancer are at increased risk for progression from latent tuberculosis infection (LTBI) to active tuberculosis (ATB) because of immunosuppression. The purpose of this study was to compare the utility of the two commonly used IGRAs, QuantiFERON-TB Gold(®) (QFT) and T-spot.TB(®) (T-spot.TB), for diagnosis of LTBI or ATB in cancer patients. METHODS: We identified patients who had an initial IGRA during 2013 and 2014 at our institution. Along with demographic information, collected clinical data included type of underlying cancer or other condition, reason for testing, diagnosis of ATB following testing, and absolute lymphocyte count (ALC) at the time of testing. IGRA results (positive, negative, borderline, or indeterminate/invalid) were compared between patients who underwent testing with either QFT or T-spot.TB. RESULTS: A total of 356 patients had 411 QFT tests done, while 737 patients had 853 T-spot.TB tests performed. The most common underlying malignancies in the QFT and T-spot.TB groups were acute myeloid leukemia (30% and 25%, respectively) and solid tumors (28% vs. 30%, respectively). The most common reasons for testing were pre-hematopoietic-cell transplantation (HCT) screening (42% with QFT and 31% with T spot.TB) or suspected pulmonary ATB (34% with QFT and 42% with T spot.TB). In the QFT group, 145/411 (35%) tests were indeterminate, while only 96/853 (11%) tests in the T-spot.TB group were invalid (P <0.001). The median ALC was 650 cells/µL in patients with an indeterminate result in the QFT group and 90 cells/µL in patients with an invalid test in the T-spot.TB group. A total of four patients were diagnosed with ATB at 1 year after testing. Figure 1 provides a flowchart describing IGRA testing results and development of ATB. CONCLUSION: The frequency of an inconclusive test result is significantly higher with QFT as compared with T-spot.TB for diagnosis of LTBI or ATB in cancer patients. A low ALC is likely a contributing factor in indeterminate QFT and invalid T spot.TBresults. [Image: see text] DISCLOSURES: E. Ariza-Heredia, Oxford Immunotec: Grant Investigator, Research grant. R. F. Chemaly, Oxford Immunotec: Consultant and Grant Investigator, Research grant. |
format | Online Article Text |
id | pubmed-6254052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62540522018-11-28 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients Kulkarni, Prathit Kmeid, Joumana Batista, Marjorie Chaer, Firas El Ariza-Heredia, Ella Graviss, Edward A Mulanovich, Victor E Chemaly, Roy F Open Forum Infect Dis Abstracts BACKGROUND: Patients with certain types of cancer are at increased risk for progression from latent tuberculosis infection (LTBI) to active tuberculosis (ATB) because of immunosuppression. The purpose of this study was to compare the utility of the two commonly used IGRAs, QuantiFERON-TB Gold(®) (QFT) and T-spot.TB(®) (T-spot.TB), for diagnosis of LTBI or ATB in cancer patients. METHODS: We identified patients who had an initial IGRA during 2013 and 2014 at our institution. Along with demographic information, collected clinical data included type of underlying cancer or other condition, reason for testing, diagnosis of ATB following testing, and absolute lymphocyte count (ALC) at the time of testing. IGRA results (positive, negative, borderline, or indeterminate/invalid) were compared between patients who underwent testing with either QFT or T-spot.TB. RESULTS: A total of 356 patients had 411 QFT tests done, while 737 patients had 853 T-spot.TB tests performed. The most common underlying malignancies in the QFT and T-spot.TB groups were acute myeloid leukemia (30% and 25%, respectively) and solid tumors (28% vs. 30%, respectively). The most common reasons for testing were pre-hematopoietic-cell transplantation (HCT) screening (42% with QFT and 31% with T spot.TB) or suspected pulmonary ATB (34% with QFT and 42% with T spot.TB). In the QFT group, 145/411 (35%) tests were indeterminate, while only 96/853 (11%) tests in the T-spot.TB group were invalid (P <0.001). The median ALC was 650 cells/µL in patients with an indeterminate result in the QFT group and 90 cells/µL in patients with an invalid test in the T-spot.TB group. A total of four patients were diagnosed with ATB at 1 year after testing. Figure 1 provides a flowchart describing IGRA testing results and development of ATB. CONCLUSION: The frequency of an inconclusive test result is significantly higher with QFT as compared with T-spot.TB for diagnosis of LTBI or ATB in cancer patients. A low ALC is likely a contributing factor in indeterminate QFT and invalid T spot.TBresults. [Image: see text] DISCLOSURES: E. Ariza-Heredia, Oxford Immunotec: Grant Investigator, Research grant. R. F. Chemaly, Oxford Immunotec: Consultant and Grant Investigator, Research grant. Oxford University Press 2018-11-26 /pmc/articles/PMC6254052/ http://dx.doi.org/10.1093/ofid/ofy210.796 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Kulkarni, Prathit Kmeid, Joumana Batista, Marjorie Chaer, Firas El Ariza-Heredia, Ella Graviss, Edward A Mulanovich, Victor E Chemaly, Roy F 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title | 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title_full | 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title_fullStr | 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title_full_unstemmed | 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title_short | 789. Comparison of Interferon-γ Release Assays (IGRAs) for Diagnosis of Latent or Active Tuberculosis in Cancer Patients |
title_sort | 789. comparison of interferon-γ release assays (igras) for diagnosis of latent or active tuberculosis in cancer patients |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254052/ http://dx.doi.org/10.1093/ofid/ofy210.796 |
work_keys_str_mv | AT kulkarniprathit 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT kmeidjoumana 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT batistamarjorie 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT chaerfirasel 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT arizaherediaella 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT gravissedwarda 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT mulanovichvictore 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients AT chemalyroyf 789comparisonofinterferongreleaseassaysigrasfordiagnosisoflatentoractivetuberculosisincancerpatients |