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Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities

PURPOSE: To comprehensively investigate prognostic factors, including clinical and molecular factors and treatment modalities, in adult glioma patients with leptomeningeal metastases (LM). METHODS: Total 226 patients with LM (from 2001 to 2021 among 1495 grade 2 to 4 glioma patients, 88.5% of LM pat...

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Autores principales: Park, Yae Won, Han, Kyunghwa, Kim, Sooyon, Kwon, Hyuk, Ahn, Sung Soo, Moon, Ju Hyung, Kim, Eui Hyun, Kim, Jinna, Kang, Seok-Gu, Chang, Jong Hee, Kim, Se Hoon, Lee, Seung-Koo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050057/
https://www.ncbi.nlm.nih.gov/pubmed/36841906
http://dx.doi.org/10.1007/s11060-022-04233-y
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author Park, Yae Won
Han, Kyunghwa
Kim, Sooyon
Kwon, Hyuk
Ahn, Sung Soo
Moon, Ju Hyung
Kim, Eui Hyun
Kim, Jinna
Kang, Seok-Gu
Chang, Jong Hee
Kim, Se Hoon
Lee, Seung-Koo
author_facet Park, Yae Won
Han, Kyunghwa
Kim, Sooyon
Kwon, Hyuk
Ahn, Sung Soo
Moon, Ju Hyung
Kim, Eui Hyun
Kim, Jinna
Kang, Seok-Gu
Chang, Jong Hee
Kim, Se Hoon
Lee, Seung-Koo
author_sort Park, Yae Won
collection PubMed
description PURPOSE: To comprehensively investigate prognostic factors, including clinical and molecular factors and treatment modalities, in adult glioma patients with leptomeningeal metastases (LM). METHODS: Total 226 patients with LM (from 2001 to 2021 among 1495 grade 2 to 4 glioma patients, 88.5% of LM patients being IDH-wildtype) with complete information on IDH mutation, 1p/19q codeletion, and MGMT promoter methylation status were enrolled. Predictors of overall survival (OS) of entire patients were determined by time-dependent Cox analysis, including clinical, molecular, and treatment data. Subgroup analyses were performed for patients with LM at initial diagnosis and LM diagnosed at recurrence (herein, initial and recurrent LM). Identical analyses were performed in IDH-wildtype glioblastoma patients. RESULTS: Median OS was 17.0 (IQR 9.7–67.1) months, with shorter median OS in initial LM than recurrent LM patients (12.2 vs 20.6 months, P < 0.001). In entire patients, chemotherapy and antiangiogenic therapy were predictors of longer OS, while male sex and initial LM were predictors of shorter OS. In initial LM, higher KPS, chemotherapy, and antiangiogenic therapy were predictors of longer OS, while male sex was a predictor of shorter OS. In recurrent LM, chemotherapy and longer interval between initial glioma and LM diagnoses were predictors of longer OS, while male sex was a predictor of shorter OS. A similar trend was observed in IDH-wildtype glioblastoma. CONCLUSION: Active chemotherapy and antiangiogenic therapy demonstrated survival benefit in glioma patients with LM. There is consistent female survival advantage, whereas longer interval between initial glioma diagnosis and LM development suggests longer OS in recurrent LM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-022-04233-y.
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spelling pubmed-100500572023-03-30 Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities Park, Yae Won Han, Kyunghwa Kim, Sooyon Kwon, Hyuk Ahn, Sung Soo Moon, Ju Hyung Kim, Eui Hyun Kim, Jinna Kang, Seok-Gu Chang, Jong Hee Kim, Se Hoon Lee, Seung-Koo J Neurooncol Research PURPOSE: To comprehensively investigate prognostic factors, including clinical and molecular factors and treatment modalities, in adult glioma patients with leptomeningeal metastases (LM). METHODS: Total 226 patients with LM (from 2001 to 2021 among 1495 grade 2 to 4 glioma patients, 88.5% of LM patients being IDH-wildtype) with complete information on IDH mutation, 1p/19q codeletion, and MGMT promoter methylation status were enrolled. Predictors of overall survival (OS) of entire patients were determined by time-dependent Cox analysis, including clinical, molecular, and treatment data. Subgroup analyses were performed for patients with LM at initial diagnosis and LM diagnosed at recurrence (herein, initial and recurrent LM). Identical analyses were performed in IDH-wildtype glioblastoma patients. RESULTS: Median OS was 17.0 (IQR 9.7–67.1) months, with shorter median OS in initial LM than recurrent LM patients (12.2 vs 20.6 months, P < 0.001). In entire patients, chemotherapy and antiangiogenic therapy were predictors of longer OS, while male sex and initial LM were predictors of shorter OS. In initial LM, higher KPS, chemotherapy, and antiangiogenic therapy were predictors of longer OS, while male sex was a predictor of shorter OS. In recurrent LM, chemotherapy and longer interval between initial glioma and LM diagnoses were predictors of longer OS, while male sex was a predictor of shorter OS. A similar trend was observed in IDH-wildtype glioblastoma. CONCLUSION: Active chemotherapy and antiangiogenic therapy demonstrated survival benefit in glioma patients with LM. There is consistent female survival advantage, whereas longer interval between initial glioma diagnosis and LM development suggests longer OS in recurrent LM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-022-04233-y. Springer US 2023-02-25 2023 /pmc/articles/PMC10050057/ /pubmed/36841906 http://dx.doi.org/10.1007/s11060-022-04233-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Park, Yae Won
Han, Kyunghwa
Kim, Sooyon
Kwon, Hyuk
Ahn, Sung Soo
Moon, Ju Hyung
Kim, Eui Hyun
Kim, Jinna
Kang, Seok-Gu
Chang, Jong Hee
Kim, Se Hoon
Lee, Seung-Koo
Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title_full Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title_fullStr Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title_full_unstemmed Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title_short Revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
title_sort revisiting prognostic factors in glioma with leptomeningeal metastases: a comprehensive analysis of clinical and molecular factors and treatment modalities
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050057/
https://www.ncbi.nlm.nih.gov/pubmed/36841906
http://dx.doi.org/10.1007/s11060-022-04233-y
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