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Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma
Background: Overall survival of patients with primary CNS lymphoma (PCNSL) has improved since the introduction of immunochemotherapy. However, up to 10-15% of PCNSL patients still die shortly after diagnosis. In the present study, we aimed to investigate the risk factors of early mortality (death wi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692612/ https://www.ncbi.nlm.nih.gov/pubmed/31417640 http://dx.doi.org/10.7150/jca.32467 |
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author | Lin, Chia-Hsin Yang, Ching-Fen Yang, Huai-Che Fay, Li-Yu Yeh, Chiu-Mei Kuan, Ai-Seon Wang, Hao-Yuan Gau, Jyh-Pyng Hsiao, Liang-Tsai Chiou, Tzeon-Jye Chen, Po-Min Liu, Yao-Chung Ko, Po-Shen Liu, Jin-Hwang Liu, Chia-Jen |
author_facet | Lin, Chia-Hsin Yang, Ching-Fen Yang, Huai-Che Fay, Li-Yu Yeh, Chiu-Mei Kuan, Ai-Seon Wang, Hao-Yuan Gau, Jyh-Pyng Hsiao, Liang-Tsai Chiou, Tzeon-Jye Chen, Po-Min Liu, Yao-Chung Ko, Po-Shen Liu, Jin-Hwang Liu, Chia-Jen |
author_sort | Lin, Chia-Hsin |
collection | PubMed |
description | Background: Overall survival of patients with primary CNS lymphoma (PCNSL) has improved since the introduction of immunochemotherapy. However, up to 10-15% of PCNSL patients still die shortly after diagnosis. In the present study, we aimed to investigate the risk factors of early mortality (death within 60 days after diagnosis) in patients with PCNSL. Methods: We included newly diagnosed PCNSL patients in a tertiary medical center in Taiwan between January 1, 2002 and May 31, 2018. Clinical risk factors were collected and compared between PCNSL patients who had and did not have early mortality. Results: A total of 133 consecutive patients with PCNSL were included in this study. Approximately 9.8% of the PCNSL patients had early mortality. In multivariate analysis, age ≥ 80 (adjusted hazard ratio [HR] 3.34, 95% confidence interval [CI] 1.01-11.04, p = 0.048) and involvement of the basal ganglia (adjusted HR 4.85, 95% CI 1.47-15.95, p = 0.009) were identified as independent risk factors of early mortality. Use of MTX-based chemotherapy served as an independent protective factor for early mortality (adjusted HR 0.19, 95% CI 0.05-0.67, p = 0.010). Infection and tumor-associated mass effect contributed most to early mortality. Conclusion: Early mortality is not uncommon in patients with PCNSL. Identification of patients with higher risk may help clinicians with initiating appropriate surveillance and management. |
format | Online Article Text |
id | pubmed-6692612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-66926122019-08-15 Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma Lin, Chia-Hsin Yang, Ching-Fen Yang, Huai-Che Fay, Li-Yu Yeh, Chiu-Mei Kuan, Ai-Seon Wang, Hao-Yuan Gau, Jyh-Pyng Hsiao, Liang-Tsai Chiou, Tzeon-Jye Chen, Po-Min Liu, Yao-Chung Ko, Po-Shen Liu, Jin-Hwang Liu, Chia-Jen J Cancer Research Paper Background: Overall survival of patients with primary CNS lymphoma (PCNSL) has improved since the introduction of immunochemotherapy. However, up to 10-15% of PCNSL patients still die shortly after diagnosis. In the present study, we aimed to investigate the risk factors of early mortality (death within 60 days after diagnosis) in patients with PCNSL. Methods: We included newly diagnosed PCNSL patients in a tertiary medical center in Taiwan between January 1, 2002 and May 31, 2018. Clinical risk factors were collected and compared between PCNSL patients who had and did not have early mortality. Results: A total of 133 consecutive patients with PCNSL were included in this study. Approximately 9.8% of the PCNSL patients had early mortality. In multivariate analysis, age ≥ 80 (adjusted hazard ratio [HR] 3.34, 95% confidence interval [CI] 1.01-11.04, p = 0.048) and involvement of the basal ganglia (adjusted HR 4.85, 95% CI 1.47-15.95, p = 0.009) were identified as independent risk factors of early mortality. Use of MTX-based chemotherapy served as an independent protective factor for early mortality (adjusted HR 0.19, 95% CI 0.05-0.67, p = 0.010). Infection and tumor-associated mass effect contributed most to early mortality. Conclusion: Early mortality is not uncommon in patients with PCNSL. Identification of patients with higher risk may help clinicians with initiating appropriate surveillance and management. Ivyspring International Publisher 2019-07-05 /pmc/articles/PMC6692612/ /pubmed/31417640 http://dx.doi.org/10.7150/jca.32467 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Lin, Chia-Hsin Yang, Ching-Fen Yang, Huai-Che Fay, Li-Yu Yeh, Chiu-Mei Kuan, Ai-Seon Wang, Hao-Yuan Gau, Jyh-Pyng Hsiao, Liang-Tsai Chiou, Tzeon-Jye Chen, Po-Min Liu, Yao-Chung Ko, Po-Shen Liu, Jin-Hwang Liu, Chia-Jen Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title | Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title_full | Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title_fullStr | Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title_full_unstemmed | Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title_short | Risk Prediction for Early Mortality in Patients with Newly Diagnosed Primary CNS Lymphoma |
title_sort | risk prediction for early mortality in patients with newly diagnosed primary cns lymphoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692612/ https://www.ncbi.nlm.nih.gov/pubmed/31417640 http://dx.doi.org/10.7150/jca.32467 |
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