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The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma

BACKGROUND: Reducing diagnostic delays in cancer has been a major interest worldwide; however, the literature on diagnostic delays in lymphoma remains scarce. Diffuse large B‐cell lymphoma (DLBCL) is the most common non‐Hodgkin's lymphoma. We aimed to determine whether certain structural factor...

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Autores principales: Zurko, Joanna C., Wade, Raymond C., Mehta, Amitkumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488145/
https://www.ncbi.nlm.nih.gov/pubmed/30884208
http://dx.doi.org/10.1002/cam4.2009
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author Zurko, Joanna C.
Wade, Raymond C.
Mehta, Amitkumar
author_facet Zurko, Joanna C.
Wade, Raymond C.
Mehta, Amitkumar
author_sort Zurko, Joanna C.
collection PubMed
description BACKGROUND: Reducing diagnostic delays in cancer has been a major interest worldwide; however, the literature on diagnostic delays in lymphoma remains scarce. Diffuse large B‐cell lymphoma (DLBCL) is the most common non‐Hodgkin's lymphoma. We aimed to determine whether certain structural factors predicted diagnostic delays in DLBCL and whether diagnostic delays impacted overall survival (OS). METHODS: Data were extracted via a retrospective cohort design from a single academic tertiary care referral center. A total of 104 patients were included. Time from first symptoms to diagnosis of <3 months was defined as “early diagnosis” and ≥3 months as “delayed diagnosis”. Analysis was performed with student's t‐test, chi‐square testing, binomial logistic regression, and Kaplan‐Meier log‐rank testing. RESULTS: “Delayed diagnosis” was more likely with lower stage, lower international prognostic index (IPI), and further distance from referral center (OR 0.66, CI 0.46‐0.95; OR 0.69, CI 0.51‐0.94; OR 1.008, CI 1.001‐1.015). Patients of “other” ethnicity and without medical insurance were more likely to have significant diagnostic delays and worse overall survival (P = 0.002 and P = 0.007, respectively). Diagnostic delays of ≥3 months did not predict worse OS. However, delays of >6 months did predict worse OS. CONCLUSION: Our data suggest that excessive diagnostic delays of more than 6 months, ethnic minority status, and uninsured status in DLBCL may lead to worse outcomes. Efforts should be undertaken to reduce excessive diagnostic delays. More investigation needs to be done on the impacts of diagnostic delays in both DLBCL and other aggressive lymphomas.
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spelling pubmed-64881452019-05-23 The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma Zurko, Joanna C. Wade, Raymond C. Mehta, Amitkumar Cancer Med Clinical Cancer Research BACKGROUND: Reducing diagnostic delays in cancer has been a major interest worldwide; however, the literature on diagnostic delays in lymphoma remains scarce. Diffuse large B‐cell lymphoma (DLBCL) is the most common non‐Hodgkin's lymphoma. We aimed to determine whether certain structural factors predicted diagnostic delays in DLBCL and whether diagnostic delays impacted overall survival (OS). METHODS: Data were extracted via a retrospective cohort design from a single academic tertiary care referral center. A total of 104 patients were included. Time from first symptoms to diagnosis of <3 months was defined as “early diagnosis” and ≥3 months as “delayed diagnosis”. Analysis was performed with student's t‐test, chi‐square testing, binomial logistic regression, and Kaplan‐Meier log‐rank testing. RESULTS: “Delayed diagnosis” was more likely with lower stage, lower international prognostic index (IPI), and further distance from referral center (OR 0.66, CI 0.46‐0.95; OR 0.69, CI 0.51‐0.94; OR 1.008, CI 1.001‐1.015). Patients of “other” ethnicity and without medical insurance were more likely to have significant diagnostic delays and worse overall survival (P = 0.002 and P = 0.007, respectively). Diagnostic delays of ≥3 months did not predict worse OS. However, delays of >6 months did predict worse OS. CONCLUSION: Our data suggest that excessive diagnostic delays of more than 6 months, ethnic minority status, and uninsured status in DLBCL may lead to worse outcomes. Efforts should be undertaken to reduce excessive diagnostic delays. More investigation needs to be done on the impacts of diagnostic delays in both DLBCL and other aggressive lymphomas. John Wiley and Sons Inc. 2019-03-18 /pmc/articles/PMC6488145/ /pubmed/30884208 http://dx.doi.org/10.1002/cam4.2009 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Zurko, Joanna C.
Wade, Raymond C.
Mehta, Amitkumar
The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title_full The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title_fullStr The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title_full_unstemmed The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title_short The impact of structural factors on diagnostic delay in diffuse large B‐cell lymphoma
title_sort impact of structural factors on diagnostic delay in diffuse large b‐cell lymphoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488145/
https://www.ncbi.nlm.nih.gov/pubmed/30884208
http://dx.doi.org/10.1002/cam4.2009
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