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  3. Loss of heterozygosity 1p36 and 19q13 is a prognostic factor for overall survival in patients with diffuse WHO grade 2 gliomas treated without chemotherapy

Loss of heterozygosity 1p36 and 19q13 is a prognostic factor for overall survival in patients with diffuse WHO grade 2 gliomas treated without chemotherapy

Details
Publisher DOI
10.1200/JCO.2006.05.9238
PubMed ID
16966689
Abstract
PURPOSE: This study was conducted to elucidate the impact of loss of heterozygosity (LOH) for chromosomes 1p36 and 19q13 on the overall survival of patients with diffusely infiltrating WHO grade 2 gliomas treated without chemotherapy. PATIENTS AND METHODS: We assessed the LOH status of tumors from patients harboring WHO grade 2 gliomas diagnosed between 1991 and 2000. Patients were either followed after initial biopsy or treated by surgery and/or radiation therapy (RT). Overall survival, time to malignant transformation, and progression-free survival were last updated as of March 2005. RESULTS: Of a total of 79 patients, LOH 1p36 and LOH 19q13 could be assessed in 67 and 66 patients, respectively. The median follow-up after diagnosis was 6 years. Loss of either 1p or 19q, in particular codeletion(s) at both loci, was found to positively impact on both overall survival (log-rank P < .01), progression-free survival, and survival without malignant transformation (P < .05). Tumor volume (P < .0001), neurologic deficits at diagnosis (P < .01), involvement of more than one lobe (P < .01), and absence of an oligodendroglial component (P < .05) were also predictors of shorter overall survival. The extent of surgery was similar in patients with or without LOH 1p and/or 19q; RT was more frequently resorted to for patients without than for patients with LOH 1p/19q (30% v 60%). CONCLUSION: The presence of LOH on either 1p36 or 19q13, and in particular codeletion of both loci is a strong, nontreatment-related, prognostic factor for overall survival in patients with diffusely infiltrating WHO grade 2 gliomas.
Date Issued
2006
Publication Type
Article
Language(s)
en
Author(s)
Mariani, Luigi  
Universitätsklinik für Neurochirurgie  
Deiana, Gianluca
Vassella, Erik  
Institut für Pathologie, Klinische Pathologie  
Fathi, Ali-Reza
Murtin, Christine
Arnold, Marlène
Vajtai, Istvan  
Institut für Pathologie  
Weis, Joachim
Siegenthaler, Peter
Schobesberger, Martina
Reinert, Michael  
Universitätsklinik für Neurochirurgie  
Additional Credits
Universitätsklinik für Neurochirurgie  
Institut für Pathologie, Klinische Pathologie  
Institut für Pathologie  
Journal
Journal of clinical oncology
Publisher
American Society of Clinical Oncology
ISSN
0732-183X
ISBN
16966689
Access(Rights)
metadata.only
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