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Clinical features and prognostic factors in 190 cancer patients with brain metastases

BACKGROUND: Brain metastases significantly reduce the survival of cancer patients. However, detailed researches on the clinical manifestations and prognoses of patients with brain metastases are lacking. The aim of this study was to investigate the clinical features and prognostic factors of cancer...

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Autores principales: Zhou, Min-Hang, Wu, Yuan, Sun, Jun-Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797847/
https://www.ncbi.nlm.nih.gov/pubmed/35117460
http://dx.doi.org/10.21037/tcr.2019.12.98
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author Zhou, Min-Hang
Wu, Yuan
Sun, Jun-Zhong
author_facet Zhou, Min-Hang
Wu, Yuan
Sun, Jun-Zhong
author_sort Zhou, Min-Hang
collection PubMed
description BACKGROUND: Brain metastases significantly reduce the survival of cancer patients. However, detailed researches on the clinical manifestations and prognoses of patients with brain metastases are lacking. The aim of this study was to investigate the clinical features and prognostic factors of cancer patients with brain metastases. METHODS: A retrospective study was conducted on patients with brain metastases who were treated in our hospital between January 2014 and January 2019. Comparison of overall survival (OS) was performed by the Kaplan-Meier method. Multivariate Cox regression models was used to identify prognostic factors for OS. RESULTS: A total of 190 patients with complete data and Eastern Cooperative Oncology Group performance status (ECOG PS) 0–2 were enrolled. Patients with brain metastases from different primary sites had significantly different survival time (P=0.001). Patients who had a longer survival time included female patients (47.4%) (34 vs. 19 months, P=0.002), those with age <65 years (63.7%) (29 vs. 18 months, P=0.002), with ECOG 0 or 1 (44.2%) (32 vs. 21 months, P=0.005), with ≤3 brain lesions (61.1%) (29 vs. 20 months, P=0.041), and with small molecular targeted therapy (48.4%) (21 vs. 18 months, P=0.006). Furthermore, multivariate analysis revealed that female, age <65 years, ≤3 brain lesions, small molecular targeted therapy were independent favorable prognostic factors of OS. CONCLUSIONS: Female, younger patients with ≤3 brain metastases predicted a better survival. To improve the poor outcomes of these patients, it is necessary to find clinically significant genetic abnormalities and administer the small molecular targeted therapy early in the course of treatment.
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spelling pubmed-87978472022-02-02 Clinical features and prognostic factors in 190 cancer patients with brain metastases Zhou, Min-Hang Wu, Yuan Sun, Jun-Zhong Transl Cancer Res Original Article BACKGROUND: Brain metastases significantly reduce the survival of cancer patients. However, detailed researches on the clinical manifestations and prognoses of patients with brain metastases are lacking. The aim of this study was to investigate the clinical features and prognostic factors of cancer patients with brain metastases. METHODS: A retrospective study was conducted on patients with brain metastases who were treated in our hospital between January 2014 and January 2019. Comparison of overall survival (OS) was performed by the Kaplan-Meier method. Multivariate Cox regression models was used to identify prognostic factors for OS. RESULTS: A total of 190 patients with complete data and Eastern Cooperative Oncology Group performance status (ECOG PS) 0–2 were enrolled. Patients with brain metastases from different primary sites had significantly different survival time (P=0.001). Patients who had a longer survival time included female patients (47.4%) (34 vs. 19 months, P=0.002), those with age <65 years (63.7%) (29 vs. 18 months, P=0.002), with ECOG 0 or 1 (44.2%) (32 vs. 21 months, P=0.005), with ≤3 brain lesions (61.1%) (29 vs. 20 months, P=0.041), and with small molecular targeted therapy (48.4%) (21 vs. 18 months, P=0.006). Furthermore, multivariate analysis revealed that female, age <65 years, ≤3 brain lesions, small molecular targeted therapy were independent favorable prognostic factors of OS. CONCLUSIONS: Female, younger patients with ≤3 brain metastases predicted a better survival. To improve the poor outcomes of these patients, it is necessary to find clinically significant genetic abnormalities and administer the small molecular targeted therapy early in the course of treatment. AME Publishing Company 2020-02 /pmc/articles/PMC8797847/ /pubmed/35117460 http://dx.doi.org/10.21037/tcr.2019.12.98 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Zhou, Min-Hang
Wu, Yuan
Sun, Jun-Zhong
Clinical features and prognostic factors in 190 cancer patients with brain metastases
title Clinical features and prognostic factors in 190 cancer patients with brain metastases
title_full Clinical features and prognostic factors in 190 cancer patients with brain metastases
title_fullStr Clinical features and prognostic factors in 190 cancer patients with brain metastases
title_full_unstemmed Clinical features and prognostic factors in 190 cancer patients with brain metastases
title_short Clinical features and prognostic factors in 190 cancer patients with brain metastases
title_sort clinical features and prognostic factors in 190 cancer patients with brain metastases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797847/
https://www.ncbi.nlm.nih.gov/pubmed/35117460
http://dx.doi.org/10.21037/tcr.2019.12.98
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