Gliomatosis Cerebri Growth Pattern: Association of Differential First-Line Treatment with Overall Survival in WHO Grade II and III Gliomas

被引:4
作者
Dive, Iris [1 ,2 ,3 ,4 ]
Steidl, Eike [2 ,4 ,6 ]
Wagner, Marlies [2 ,3 ,4 ,6 ]
Filipski, Katharina [2 ,3 ,4 ,5 ]
Burger, Michael C. [1 ,2 ,3 ,4 ]
Franz, Kea [1 ,2 ,3 ,4 ,7 ]
Harter, Patrick N. [2 ,3 ,4 ,5 ]
Bahr, Oliver [1 ,2 ,3 ,4 ]
Fokas, Emmanouil [2 ,3 ,4 ,8 ]
Herrlinger, Ulrich [9 ]
Steinbach, Joachim P. [1 ,2 ,3 ,4 ]
机构
[1] Goethe Univ, Dr Senckenberg Inst Neurooncol, Schleusenweg 2-16, DE-60528 Frankfurt, Germany
[2] Goethe Univ, Univ Canc Ctr Frankfurt UCT, Frankfurt, Germany
[3] Goethe Univ, Frankfurt Canc Inst FCI, Frankfurt, Germany
[4] German Canc Consortium DKTK, Partner Site Frankfurt Mainz, Frankfurt, Germany
[5] Goethe Univ, Inst Neurol, Edinger Inst, Frankfurt, Germany
[6] Goethe Univ, Inst Neuroradiol, Frankfurt, Germany
[7] Goethe Univ, Dept Neurosurg, Frankfurt, Germany
[8] Goethe Univ, Dept Radiotherapy & Oncol, Frankfurt, Germany
[9] Univ Med Ctr Bonn, Dept Neurol, Bonn, Germany
关键词
Low-grade glioma; Gliomatosis cerebri; First-line treatment; Overall survival; TERM-FOLLOW-UP; PROCARBAZINE; CHEMOTHERAPY; VINCRISTINE; MANAGEMENT; LOMUSTINE; PROGNOSIS; TRIAL;
D O I
10.1159/000512562
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Gliomatosis cerebri (GC) is defined by diffuse, widespread glial tumor growth affecting three or more cerebral lobes. Previous studies in gliomas found no distinct histological or molecular GC subtype, yet the presence of GC is associated with worse median overall survival (OS). Here, we explored whether differing therapeutic strategies in first-line treatment could account for this. Methods: From our University Cancer Center database, 47 patients with histological diagnosis of WHO grade II or III glioma and GC imaging pattern were identified. GC criteria were confirmed by independent review. Patients with WHO grade II or III glioma with non-GC pattern served as control cohort (n = 343). Results: Within the GC patient cohort, lower WHO grade, mutated isocitrate dehydrogenase 1 (IDH1) status, and absence of contrast enhancement were associated with better OS. Compared to the control cohort, patients with GC had significantly shorter OS independent of histological diagnosis or IDH1 mutation status. Patients with GC preferentially received chemotherapy alone (62 vs. 18%), and less frequently radiochemotherapy (21 vs. 27%). OS was significantly shorter in the GC cohort compared to the non-GC cohort both for chemotherapy (3.9 vs. 7.6 years, p = 0.0085) and for combined radiochemotherapy (1.1 vs. 8.4 years, p < 0.0001). However, when only patients who received biopsy plus chemotherapy were analyzed, the differences lost statistical significance (3.5 vs. 6.6 years, p = 0.196). Conclusion: We found major differences in the selection of first-line therapies of GC versus non-GC patients. Our results suggest that these differences may partly account for the worse prognosis of GC patients.
引用
收藏
页码:215 / 224
页数:10
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