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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6488145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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