Antiangiogenic Agents for Nonmalignant Brain Tumors

被引:34
|
作者
Hawasli, Ammar H. [1 ]
Rubin, Joshua B. [2 ,5 ]
Tran, David D. [6 ]
Adkins, Douglas R. [6 ]
Waheed, Shahid [7 ]
Hullar, Timothy E. [3 ,5 ]
Gutmann, David H. [4 ]
Evans, John [1 ]
Leonard, Jeffrey R. [1 ]
Zipfel, Gregory J. [1 ]
Chicoine, Michael R. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Neurosurg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Otolaryngol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Med, Div Oncol, St Louis, MO 63110 USA
[7] JB & Greeta B Arthur Canc Ctr, Mexico, MO USA
关键词
brain tumor; meningioma; vestibular schwannoma; vascular endothelial growth factor; neurofibromatosis; bevacizumab; pazopanib; VESTIBULAR SCHWANNOMA; NEUROFIBROMATOSIS TYPE-2; BEVACIZUMAB; MENINGIOMAS; VEGF; REGRESSION; EXPRESSION; THERAPY;
D O I
10.1055/s-0033-1338262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To assess the treatment response and side effects for the use of antiangiogenic agents such as vascular endothelial growth factor (VEGF) inhibitors for patients with vestibular schwannomas and meningiomas. Design and Methods Retrospective review of eight male and two female patients (ages 14 to 70, mean 36 years), treated with bevacizumab (9) or pazopanib (1). Six patients had neurofibromatosis type 2 (NF2) with bilateral vestibular schwannomas and meningiomas, and the four others had aggressive recurrent meningiomas. Results During treatment (range 4 to 21 months, mean 9.1) with antiangiogenic agents, two patients with an atypical meningioma and radiation necrosis had dramatic partial response, the six NF2 patients had stable or slightly improved disease, and two meningioma patients had disease progression. Hearing was stable in three of the NF2 patients and was improved in three NF2 patients (one of whom received a cochlear implant). Minor toxicities included epistaxis, nausea, diarrhea, weight loss, and abdominal pain. No grade 3 or 4 toxicities were observed. Conclusion Antiangiogenic agents appear to be safe for the treatment of patients with nonmalignant brain tumors, and in select cases may be efficacious.
引用
收藏
页码:136 / 141
页数:6
相关论文
共 50 条
  • [41] Molecular imaging of antiangiogenic agents
    Rehman, S
    Jayson, GC
    ONCOLOGIST, 2005, 10 (02): : 92 - 103
  • [42] Antiangiogenic agents for the treatment of glioblastoma
    Gerstner, Elizabeth R.
    Duda, Dan G.
    di Tomaso, Emmanuelle
    Sorensen, Greg
    Jain, Rakesh K.
    Batchelor, Tracy T.
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (12) : 1895 - 1908
  • [43] Antiangiogenic agents and targets: A perspective
    Teicher, Beverly A.
    BIOCHEMICAL PHARMACOLOGY, 2011, 81 (01) : 6 - 12
  • [44] A patent perspective of antiangiogenic agents
    Zhang, Junyu
    Wang, Jin
    Li, Yanchen
    Pan, Xiaoyan
    Qu, Jingkun
    Zhang, Jie
    EXPERT OPINION ON THERAPEUTIC PATENTS, 2023, 33 (12) : 821 - 840
  • [45] Interferons as antiangiogenic agents.
    Lindner D.J.
    Current Oncology Reports, 2002, 4 (6) : 510 - 514
  • [46] Understanding resistance to antiangiogenic agents
    Sarah Crunkhorn
    Nature Reviews Drug Discovery, 2014, 13 (10) : 726 - 726
  • [47] Antiangiogenic agents in breast cancer
    Salter, John T.
    Miller, Kathy D.
    CANCER INVESTIGATION, 2007, 25 (07) : 518 - 526
  • [48] Analysis of Toxic Effects With Antiangiogenic Agents Plus Stereotactic Body Radiation in Ultracentral Lung Tumors
    Wang, Chunyu
    Rimner, Andreas
    Gelblum, Daphna Y.
    Flynn, Jessica
    Jackson, Andrew
    Yorke, Ellen
    Wu, Abraham J.
    JAMA ONCOLOGY, 2019, 5 (05) : 737 - 739
  • [49] NEW AGENTS IN THE TREATMENT OF PRIMARY BRAIN-TUMORS
    TAYLOR, SA
    JOURNAL OF NEURO-ONCOLOGY, 1994, 20 (02) : 141 - 153
  • [50] Molecularly Targeted Agents in the Therapy of Pediatric Brain Tumors
    Miriam Bornhorst
    Eugene I. Hwang
    Pediatric Drugs, 2020, 22 : 45 - 54