Prognostic factors in recurrent glioblastoma patients treated with bevacizumab

被引:21
|
作者
Schaub, Christina [1 ]
Tichy, Julia [2 ]
Schaefer, Niklas [1 ,3 ]
Franz, Kea [4 ]
Mack, Frederic [1 ]
Mittelbronn, Michel [5 ]
Kebir, Sied [1 ,3 ]
Thiepold, Anna-Luisa [2 ]
Waha, Andreas [6 ]
Filmann, Natalie [7 ]
Banat, Mohammed [8 ]
Fimmers, Rolf [9 ]
Steinbach, Joachim P. [2 ]
Herrlinger, Ulrich [1 ]
Rieger, Johannes [2 ]
Glas, Martin [1 ,3 ,10 ]
Baehr, Oliver [2 ]
机构
[1] Univ Bonn, Div Clin Neurooncol, Dept Neurol, Med Ctr, Sigmund Freud Str 25, D-53105 Bonn, Germany
[2] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Dr Senckenberg Inst Neurooncol, Schleusenweg 2-16, D-60528 Frankfurt, Germany
[3] Univ Bonn, Inst Reconstruct Neurobiol, Stem Cell Pathol Grp, Med Ctr, Bonn, Germany
[4] Goethe Univ Hosp, Dept Neurosurg, Frankfurt, Germany
[5] Goethe Univ Hosp, Inst Neurol, Edinger Inst, Frankfurt, Germany
[6] Univ Bonn, Inst Neuropathol, Med Ctr, Bonn, Germany
[7] Goethe Univ Hosp Frankfurt, Inst Biostat & Math Modeling, Frankfurt, Germany
[8] Univ Bonn, Dept Neurosurg, Med Ctr, Bonn, Germany
[9] Univ Bonn, Inst Med Biometry Informat & Epidemiol, Med Ctr, Bonn, Germany
[10] MediClin Robert Janker Klin, Clin Cooperat Unit Neurooncol, Bonn, Germany
关键词
Recurrent glioblastoma; Bevacizumab; Irinotecan; Survival; Karnofsky performance score; SINGLE-AGENT BEVACIZUMAB; PHASE-II; PLUS IRINOTECAN; TEMOZOLOMIDE; TRIAL; RADIOTHERAPY; THERAPY; CHEMOTHERAPY; RADIATION;
D O I
10.1007/s11060-016-2144-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The value of bevacizumab (BEV) in recurrent glioblastoma is unclear. Imaging parameters and progression-free survival (PFS) are problematic endpoints. Few data exist on clinical factors influencing overall survival (OS) in unselected patients with recurrent glioblastoma exposed to BEV. We retrospectively analyzed 174 patients with recurrent glioblastoma treated with BEV at two German brain tumor centers. We evaluated general patient characteristics, MGMT status, pretreatment, concomitant oncologic treatment and overall survival. Karnofsky performance score, number of prior chemotherapies, number of prior recurrences and combined treatment with irinotecan (IRI) were significantly associated with OS in univariate analysis. We did not find differences in OS related to sex, age, histology, MGMT status, prior surgical treatment or number of prior radiotherapies. Combined treatment with IRI and higher KPS both remained significantly associated with prolonged survival in multivariate analysis, but patients receiving IRI co-treatment had less advanced disease. Grouping into clinically relevant categories revealed an OS of 16.9 months from start of BEV in patients with first recurrence and KPS aeyen 80 % (n = 25). In contrast, in patients with second recurrence and KPS < 80 %, OS was 3.6 months (n = 27). Our observational data support an early use of BEV in patients with good performance status. The benefit of co-treatment with IRI in our cohort seems to be the result of biased patient recruitment.
引用
收藏
页码:93 / 100
页数:8
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