Literature DB >> 30711992

Leptomeningeal Gliomatosis: A Single Institution Study of 31 Patients.

Didier Autran1, Maryline Barrie2, Mona Matta2, Colette Monserrat3, Chantal Campello2, Gregorio Petrirena2, Celine Boucard2, Laetitia Padovani4, Anderson Loundou5, Romain Appay6, Thomas Graillon7, Henry Dufour7, Dominique Figarella-Branger6,8, Olivier Chinot2,8, Emeline Tabouret2,8.   

Abstract

BACKGROUND/AIM: Secondary leptomeningeal gliomatosis (LG) is a rare and severe progression pattern of glioma. Our objective was to evaluate the characteristics and outcome of patients with LG. PATIENTS AND METHODS: We retrospectively reviewed 31 patients diagnosed with secondary LG. At the time of LG diagnosis, the median age of patients was 45 years. The histological grade was IV in 20 patients and II to III in 11 patients. As a first-line of therapy for LG, 22 patients received an oncological treatment: i) BCNU-temozolomide (TMZ) (n=15), ii) other type of chemotherapy (n=7), and iii) no treatment (supportive care) (n=9).
RESULTS: Following LG diagnosis, the median progression-free survival (PFS) and overall survival (OS) were 1.8 months [95% confidence interval (CI)=0.9-2.7] and 2.1 months (95%CI=1.3-3), respectively. The univariate analyses showed an improved OS with age of less than 45 years (p<0.001), a prolonged interval from the initial glioma diagnosis (IGD) to LG diagnosis (p=0.003), BCNU-TMZ as the preferred first-line treatment for LG out of the three options (p=0.008), and Karnofsky performance status (KPS) ≥70 (p=0.012). Prolonged interval from IGD to LG diagnosis (HR=5.839) and BCNU-TMZ as the chosen first-line treatment for LG (HR=6.635) remained significant in the multivariate analyses as well. Among the 22 treated patients, the median OS was significantly higher (p=0.008) with the BCNU-TMZ treatment (5.7 months; 95%CI=4.2-7.1), compared to other types of treatment offered (2 months; 95%CI=1.1-2.9).
CONCLUSION: The time interval from the IGD to the LG diagnosis is a potential prognostic factor for LG. BCNU-TMZ may be a therapeutic option in the present setting. Copyright
© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Entities:  

Keywords:  BCNU; Glioma; leptomeningeal gliomatosis; prognostic factors; temozolomide

Mesh:

Substances:

Year:  2019        PMID: 30711992     DOI: 10.21873/anticanres.13210

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  4 in total

Review 1.  Leptomeningeal Spread in Glioblastoma: Diagnostic and Therapeutic Challenges.

Authors:  Cristina Birzu; Suzanne Tran; Franck Bielle; Mehdi Touat; Karima Mokhtari; Nadia Younan; Dimitri Psimaras; Khe Hoang-Xuan; Marc Sanson; Jean-Yves Delattre; Ahmed Idbaih
Journal:  Oncologist       Date:  2020-08-31

2.  Intrathecal methotrexate in combination with systemic chemotherapy in glioblastoma patients with leptomeningeal dissemination: A retrospective analysis.

Authors:  Xun Kang; Feng Chen; Shou-Bo Yang; Ya-Li Wang; Zeng-Hui Qian; Yan Li; Hao Lin; Parker Li; Yi-Chen Peng; Xiao-Min Wang; Wen-Bin Li
Journal:  World J Clin Cases       Date:  2022-06-16       Impact factor: 1.534

3.  Leptomeningeal Spread at the Diagnosis of Glioblastoma Multiforme: A Case Report and Literature Review.

Authors:  Cheolwon Jang; Byung-Kyu Cho; Sung Hwan Hwang; Hyung Jin Shin; Sang Hoon Yoon
Journal:  Brain Tumor Res Treat       Date:  2022-07

4.  Screening seven hub genes associated with prognosis and immune infiltration in glioblastoma.

Authors:  Yesen Zhang; Huasheng Fan; Chun Zou; Feng Wei; Jiwei Sun; Yuchun Shang; Liechun Chen; Xiangyu Wang; Beiquan Hu
Journal:  Front Genet       Date:  2022-08-12       Impact factor: 4.772

  4 in total

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