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Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer
BACKGROUND: To investigate whether whole‐brain radiotherapy (WBRT) decreases lymphocyte counts and evaluate the impact of treatment‐related lymphopenia on survival in patients with brain metastasis. METHODS: Medical records from 60 small‐cell lung cancer patients treated with WBRT from January 2010...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175032/ https://www.ncbi.nlm.nih.gov/pubmed/36994596 http://dx.doi.org/10.1111/1759-7714.14868 |
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author | Lin, Yu‐Jung Kang, Yu‐Mei Wu, Yuan‐Hung Chen, Yi‐Wei Hu, Yu‐Wen |
author_facet | Lin, Yu‐Jung Kang, Yu‐Mei Wu, Yuan‐Hung Chen, Yi‐Wei Hu, Yu‐Wen |
author_sort | Lin, Yu‐Jung |
collection | PubMed |
description | BACKGROUND: To investigate whether whole‐brain radiotherapy (WBRT) decreases lymphocyte counts and evaluate the impact of treatment‐related lymphopenia on survival in patients with brain metastasis. METHODS: Medical records from 60 small‐cell lung cancer patients treated with WBRT from January 2010 to December 2018 were included in the study. Total lymphocyte count (TLC) was obtained pre and post treatment (within 1 month). We performed linear and logistic regression analyses to identify predictors of lymphopenia. The association between lymphopenia and survival was analyzed using Cox regression analysis. RESULTS: Thirty‐nine patients (65%) developed treatment‐related lymphopenia. The median TLC decrease was −374 cells/μL (interquartile range −50 to −722, p < 0.001). Baseline lymphocyte count was a significant predictor of TLC difference and percentage change in TLC. Logistic regression analysis found male sex (odds ratio [OR] 0.11, 95% confidence interval [CI] 0.00–0.79, p = 0.033) and higher baseline lymphocyte count (OR 0.91, 95% CI 0.82–0.99, p = 0.005) were associated with a lower risk of developing ≥grade 2 treatment‐related lymphopenia. Cox regression analysis showed that age at brain metastasis (hazard ratio [HR] 1.03, 95% CI 1.01–1.05, p = 0.013), ≥grade 2 treatment‐related lymphopenia, and percentage change in TLC (per 10%, HR 0.94, 95% CI 0.89–0.99, p = 0.032) were prognostic factors of survival. CONCLUSIONS: WBRT decreases TLC and the magnitude of treatment‐related lymphopenia is an independent predictor of survival in small‐cell lung cancer patients. |
format | Online Article Text |
id | pubmed-10175032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-101750322023-05-12 Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer Lin, Yu‐Jung Kang, Yu‐Mei Wu, Yuan‐Hung Chen, Yi‐Wei Hu, Yu‐Wen Thorac Cancer Original Articles BACKGROUND: To investigate whether whole‐brain radiotherapy (WBRT) decreases lymphocyte counts and evaluate the impact of treatment‐related lymphopenia on survival in patients with brain metastasis. METHODS: Medical records from 60 small‐cell lung cancer patients treated with WBRT from January 2010 to December 2018 were included in the study. Total lymphocyte count (TLC) was obtained pre and post treatment (within 1 month). We performed linear and logistic regression analyses to identify predictors of lymphopenia. The association between lymphopenia and survival was analyzed using Cox regression analysis. RESULTS: Thirty‐nine patients (65%) developed treatment‐related lymphopenia. The median TLC decrease was −374 cells/μL (interquartile range −50 to −722, p < 0.001). Baseline lymphocyte count was a significant predictor of TLC difference and percentage change in TLC. Logistic regression analysis found male sex (odds ratio [OR] 0.11, 95% confidence interval [CI] 0.00–0.79, p = 0.033) and higher baseline lymphocyte count (OR 0.91, 95% CI 0.82–0.99, p = 0.005) were associated with a lower risk of developing ≥grade 2 treatment‐related lymphopenia. Cox regression analysis showed that age at brain metastasis (hazard ratio [HR] 1.03, 95% CI 1.01–1.05, p = 0.013), ≥grade 2 treatment‐related lymphopenia, and percentage change in TLC (per 10%, HR 0.94, 95% CI 0.89–0.99, p = 0.032) were prognostic factors of survival. CONCLUSIONS: WBRT decreases TLC and the magnitude of treatment‐related lymphopenia is an independent predictor of survival in small‐cell lung cancer patients. John Wiley & Sons Australia, Ltd 2023-03-30 /pmc/articles/PMC10175032/ /pubmed/36994596 http://dx.doi.org/10.1111/1759-7714.14868 Text en © 2023 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Lin, Yu‐Jung Kang, Yu‐Mei Wu, Yuan‐Hung Chen, Yi‐Wei Hu, Yu‐Wen Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title | Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title_full | Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title_fullStr | Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title_full_unstemmed | Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title_short | Lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
title_sort | lymphocytopenia and survival after whole‐brain radiotherapy in patients with small‐cell lung cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175032/ https://www.ncbi.nlm.nih.gov/pubmed/36994596 http://dx.doi.org/10.1111/1759-7714.14868 |
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