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Recursive partitioning analysis of prognostic factors for glioblastoma patients aged 70 years or older

Authors :
Pascale Fabbro-Peray
Luc Taillandier
Anna R. Cooper
Michael A. Vogelbaum
Lakshmi Nayak
Sonia Zouaoui
Lauren E. Abrey
Samuel T. Chao
John H. Suh
Valérie Rigau
Lisa M. DeAngelis
Tyler J. Fraum
David M. Peereboom
Joanna H. Shih
Luc Bauchet
Fabio M. Iwamoto
Hélène Mathieu-Daudé
Jacob G. Scott
Source :
Cancer. 118:5595-5600
Publication Year :
2012
Publisher :
Wiley, 2012.

Abstract

The most-used prognostic scheme for malignant gliomas included only patients aged 18 to 70 years. The purpose of this study was to develop a prognostic model for patients ≥70 years of age with newly diagnosed glioblastoma.A total of 437 patients ≥70 years of age with newly diagnosed glioblastoma, pooled from 2 tertiary academic institutions, was identified for recursive partitioning analysis (RPA). The resulting prognostic model, based on the final pruned RPA tree, was validated using 265 glioblastoma patients ≥70 years of age from a data set independently compiled by a French consortium.RPA produced 9 terminal nodes, which were pruned to 4 prognostic subgroups with markedly different median survivals: subgroup I = patients75.5 years of age who underwent surgical resection (9.3 months); subgroup II = patients ≥75.5 years of age who underwent surgical resection (6.4 months); subgroup III = patients with Karnofsky performance status of 70 to 100 who underwent biopsy only (4.6 months); and subgroup IV = patients with Karnofsky performance status70 who underwent biopsy only (2.3 months). Application of this prognostic model to the French cohort also resulted in significantly different (P.0001) median survivals for subgroups I (8.5 months), II (7.7 months), III (4.3 months), and IV (3.1 months).This model divides elderly glioblastoma patients into prognostic subgroups that can be easily implemented in both the patient care and the clinical trial settings. This purely clinical prognostic model serves as a backbone for the future incorporation of the increasing number of potential molecular prognostic markers.

Details

ISSN :
0008543X
Volume :
118
Database :
OpenAIRE
Journal :
Cancer
Accession number :
edsair.doi.dedup.....41eedbc0ceee6ed1f8d32f5811614918