Literature DB >> 12595806

[Glioblastomas: clinical study and search for prognostic factors].

J-F Mineo1, I Quintin-Roue, B Lucas, V Buburusan, G Besson.   

Abstract

Glioblastoma multiform is one of the most devastating primary tumors in neurooncology. We analyzed prognosis factors in patients with grade IV glioblastoma treated between 1993 and 1997. The 22 long-term survival patients (survival over 26 months) were extracted from our 30 years archives and the 2 populations are compared. The incidence was 2.6/100,000h/year, 62% male and 38% female, mean age 59 years, mean survival 12 months, median survival time 9 months. Multivariate analysis showed that younger age, surgical treatment and radiotherapy were all dependent prognosis factors for better survival. Statistically, survival was best for total surgical removal of tumors, followed by tumor gross resection then biopsy. Clinical status and inextirpable tumor location were also prognosis factors. The free interval time between total surgery and tumor reappearance was strongly correlated with survival (r=0.94). This suggests that some grade IV gliomas follow a quicker course, others exhibiting slow growth. Each of the prognosis factors was confirmed in the long-survival patients. Prevalence of all glioblastomes was 4.3%. Their mean age was 42 and mean survival 62 months. A larger proportion of these patients had total surgery and radiotherapy. The time lapse before tumor reappearance was longer. Deep tumor locations were less frequent. The proportion of secondary versus primary glioblastomas was the greatest difference between the long-term and regular survivors. Secondary glioblastomas were found in only 4% of the standard population and in 23 to 41% in the long-term survivors (p<0.01). Primary glioblastomas typically show EGFR over expression and mutation (variant III). The pathway to secondary glioblastoma involves early P53 mutation. Despite the fact that the anatomopathologist regards similar tissues under the microscope, these subtypes of glioblastomas are distinct disease entities which evolve through different genetic pathways and exhibit different outcomes.

Entities:  

Mesh:

Year:  2002        PMID: 12595806

Source DB:  PubMed          Journal:  Neurochirurgie        ISSN: 0028-3770            Impact factor:   1.553


  10 in total

1.  Increasing of HER2 membranar density in human glioblastoma U251MG cell line established in a new nude mice model.

Authors:  Jean-François Mineo; Anne Bordron; Isabelle Quintin-Roué; Quintin-Roué Isabelle; Claude-Alain Maurage; Virginie Buhé; Buhé Virginie; Séverine Loisel; Loisel Séverine; François Dubois; Serge Blond; Christian Berthou
Journal:  J Neurooncol       Date:  2006-02       Impact factor: 4.130

2.  ADAM17 promotes glioma cell malignant phenotype.

Authors:  Xuguang Zheng; Feng Jiang; Mark Katakowski; Yong Lu; Michael Chopp
Journal:  Mol Carcinog       Date:  2011-04-07       Impact factor: 4.784

3.  Low HER2-expressing glioblastomas are more often secondary to anaplastic transformation of low-grade glioma.

Authors:  Jean-François Mineo; Anne Bordron; Marc Baroncini; Claude-Alain Maurage; Carole Ramirez; Rose-Mary Siminski; Christian Berthou; Phong Dam Hieu
Journal:  J Neurooncol       Date:  2007-06-15       Impact factor: 4.130

4.  Pediatric glioblastoma: clinico-radiological profile and factors affecting the outcome.

Authors:  Kuntal Kanti Das; Anant Mehrotra; Anup P Nair; Shaleen Kumar; Arun K Srivastava; Rabi N Sahu; Raj Kumar
Journal:  Childs Nerv Syst       Date:  2012-08-19       Impact factor: 1.475

5.  ADAM17 promotes breast cancer cell malignant phenotype through EGFR-PI3K-AKT activation.

Authors:  Xuguang Zheng; Feng Jiang; Mark Katakowski; Zheng Gang Zhang; Qing-e Lu; Michael Chopp
Journal:  Cancer Biol Ther       Date:  2009-06-25       Impact factor: 4.742

6.  Long-term survival with primary glioblastoma multiforme: a clinical study in bulgarian patients.

Authors:  E Naydenov; C Tzekov; K Minkin; S Nachev; K Romansky; V Bussarsky
Journal:  Case Rep Oncol       Date:  2011-01-04

7.  Overexpression of miR‑145 in U87 cells reduces glioma cell malignant phenotype and promotes survival after in vivo implantation.

Authors:  Yong Lu; Michael Chopp; Xuguang Zheng; Mark Katakowski; Ding Wang; Elise Fraser; Monique Nguyen; Feng Jiang
Journal:  Int J Oncol       Date:  2014-12-23       Impact factor: 5.650

8.  Recombinant humanised anti-HER2/neu antibody (Herceptin) induces cellular death of glioblastomas.

Authors:  J-F Mineo; A Bordron; I Quintin-Roué; S Loisel; K L Ster; V Buhé; N Lagarde; C Berthou
Journal:  Br J Cancer       Date:  2004-09-13       Impact factor: 7.640

9.  Long-Term Survival of a Patient with Giant Cell Glioblastoma: Case Report and Review of the Literature.

Authors:  E Naydenov; V Bussarsky; S Nachev; S Hadjidekova; D Toncheva
Journal:  Case Rep Oncol       Date:  2009-07-17

10.  Giant cells glioblastoma: case report and pathological analysis from this uncommon subtype of glioma.

Authors:  Telmo A B Belsuzarri; João F M Araujo; Aguinaldo P Catanoce; Maick W F Neves; Rodrigo A S Sola; Juliano N Navarro; Leandro G Brito; Nilton R Silva; Luis Otavio C Pontelli; Luiz Gustavo A Mattos; Tiago F Gonçales; Wolnei M Zeviani; Renata M B Marques
Journal:  Rare Tumors       Date:  2015-03-26
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.