Antiangiogenic therapy using bevacizumab in recurrent high-grade glioma: impact on local control and patient survival

被引:191
作者
Narayana, Ashwatha [1 ]
Kelly, Patrick [2 ]
Golfinos, John [2 ]
Parker, Erik [2 ]
Johnson, Glyn [3 ]
Knopp, Edmond [3 ]
Zagzag, David [5 ]
Fischer, Ingeborg [5 ]
Raza, Shahzad [1 ]
Medabalmi, Praveen [4 ]
Eagan, Patricia [6 ,7 ]
Gruber, Michael L. [2 ,6 ,7 ]
机构
[1] NYU, Med Ctr, Dept Radiat Oncol, New York, NY 11016 USA
[2] NYU, Med Ctr, Dept Neurosurg, New York, NY 11016 USA
[3] NYU, Med Ctr, Dept Radiol, New York, NY 11016 USA
[4] NYU, Med Ctr, Dept Biostat, New York, NY 11016 USA
[5] NYU, Med Ctr, Dept Pathol, New York, NY 11016 USA
[6] NYU, Med Ctr, Dept Neurooncol, New York, NY 11016 USA
[7] Overlook Hosp, Summit, NJ USA
关键词
antiangiogenic therapy; bevacizumab; high-grade glioma; ENDOTHELIAL GROWTH-FACTOR; PHASE-II TRIAL; MALIGNANT GLIOMA; PLUS IRINOTECAN; FACTOR VEGF; CANCER; CELLS; GLIOBLASTOMA; TEMOZOLOMIDE; ANGIOGENESIS;
D O I
10.3171/2008.4.17492
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Antiangiogenic agents have recently shown impressive radiological responses in high-grade glioma. However, it is not clear if the responses are related to vascular changes or due to antitumoral effects. The authors report the mature results of a clinical study of bevacizumab-based treatment of recurrent high-grade gliomas. Methods. Sixty-one patients with recurrent high-grade gliomas received treatment with bevacizumab at 10 mg/ kg every 2 weeks for 4 doses in an 8-week cycle along with either irinotecan or carboplatin. The choice of concomitant chemotherapeutic agent was based on the number of recurrences and prior chemotherapy. Results. At a median follow-up of 7.5 months (range 1-19 months), 50 (82%) of 61 patients relapsed and 42 patients (70%) died of the disease. The median number of administered bevacizumab cycles was 2 (range 1-7 cycles). The median progression-free survival (PFS) and overall survival (OS) were 5 (95% confidence interval [CI] 2.3-7.7) and 9 (95% CI 7.6-10.4) months, respectively, as calculated from the initiation of the bevacizumab-based therapy. Radiologically demonstrated responses following therapy were noted in 73.6% of cases. Neither the choice of chemotherapeutic agent nor the performance of a resection prior to therapy had an impact on patient survival. Although the predominant pattern of relapse was local, 15 patients (30%) had diffuse disease. Conclusions. Antiangiogenic therapy using bevacizumab appears to improve Survival in patients with recurrent high-grade glioma. A possible change in the invasiveness of the tumor following therapy is worrisome and Must be closely monitored. (DOI: 10.3171/2008.4.17492)
引用
收藏
页码:173 / 180
页数:8
相关论文
共 28 条
[11]   RESPONSE CRITERIA FOR PHASE-II STUDIES OF SUPRATENTORIAL MALIGNANT GLIOMA [J].
MACDONALD, DR ;
CASCINO, TL ;
SCHOLD, SC ;
CAIRNCROSS, JG .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (07) :1277-1280
[12]   Drug Insight: temozolomide as a treatment for malignant glioma - impact of a recent trial [J].
Mason, WP ;
Cairncross, JG .
NATURE CLINICAL PRACTICE NEUROLOGY, 2005, 1 (02) :88-95
[13]   Intensity-modulated radiotherapy in high-grade gliomas: Clinical and dosimetric results [J].
Narayana, A ;
Yamada, J ;
Berry, S ;
Shah, P ;
Hunt, M ;
Gutin, PH ;
Leibel, SA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 64 (03) :892-897
[14]  
Narayana A, 2007, J CLIN ONCOL, V25
[15]  
Narayana A, 2004, TXB RAD ONCOLOGY, P471
[16]   MRI in patients with high-grade gliomas treated with bevacizumab and chemotherapy [J].
Pope, WB ;
Lai, A ;
Nghiemphu, P ;
Mischel, P ;
Cloughesy, TF .
NEUROLOGY, 2006, 66 (08) :1258-1260
[17]  
Raizer JJ, 2007, J CLIN ONCOL, V25
[18]   Angiogenesis-independent tumor growth mediated by stem-like cancer cells [J].
Sakariassen, Per O. ;
Prestegarden, Lars ;
Wang, Jian ;
Skaftnesmo, Kai-Ove ;
Mahesparan, Rupavathana ;
Molthoff, Carla ;
Sminia, Peter ;
Sundlisaeter, Eirik ;
Misra, Anjan ;
Tysnes, Berit Bolge ;
Chekenya, Martha ;
Peters, Hans ;
Lende, Gabriel ;
Henning Kalland, Karl ;
Oyan, Anne M. ;
Petersen, Kjell ;
Jonassen, Inge ;
van der Kogel, Albert ;
Feuerstein, Burt G. ;
Terzis, A. Jorge A. ;
Bjerkvig, Rolf ;
Enger, Per Oyvind .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (44) :16466-16471
[19]   Incorporation of bone marrow-derived Flk-1-expressing CD34+ cells in the endothelium of tumor vessels in the mouse brain [J].
Santarelli, Justin G. ;
Udani, Vikram ;
Yung, Yun C. ;
Cheshier, Sam ;
Wagers, Amy ;
Brekken, Rolf A. ;
Weissman, Irving ;
Tse, Victor .
NEUROSURGERY, 2006, 59 (02) :374-381
[20]   Monoclonal antibodies to vascular endothelial growth factor (VEGF) and the VEGF receptor, FLT-1, inhibit the growth of C6 glioma in a mouse xenograft [J].
Stefanik, DF ;
Fellows, WK ;
Rizkalla, LR ;
Rizkalla, WM ;
Stefanik, PP ;
Deleo, AB ;
Welch, WC .
JOURNAL OF NEURO-ONCOLOGY, 2001, 55 (02) :91-100