Rechallenging Recurrent Glioblastoma with Intra-Arterial Bevacizumab with Blood Brain-Barrier Disruption Results in Radiographic Response

被引:12
|
作者
Faltings, Lukas [1 ]
Kulason, Kay O. [1 ]
Patel, Nitesh, V [1 ]
Wong, Tamika [2 ]
Fralin, Sherese [2 ]
Li, Mona [2 ]
Schneider, Julia R. [1 ]
Filippi, Christopher G. [3 ,4 ]
Langer, David J. [1 ,2 ]
Ortiz, Rafael [1 ,2 ]
Boockvar, John A. [1 ,2 ]
机构
[1] Lenox Hill Hosp, Zucker Sch Med Hofstra Northwell, Dept Neurosurg, New York, NY 10021 USA
[2] Lenox Hill Hosp, Dept Neurosurg, Brain Tumor Ctr, New York, NY 10021 USA
[3] Lenox Hill Hosp, Dept Radiol, Div Neuroradial, New York, NY 10021 USA
[4] Zucker Sch Med Hofstra Northwell, Dept Radiol, Manhasset, NY USA
关键词
Bevacizumab; Blood-brain barrier disruption; Glioblastoma; Intra-arterial; Recurrent GBM; Vascular endothelial growth factor; ANTIANGIOGENIC THERAPY; ADJUVANT TEMOZOLOMIDE; CEREBRAL INFUSION; MALIGNANT GLIOMA; RADIOTHERAPY; PROGRESSION; CONCOMITANT; IRINOTECAN; RESISTANT; SURVIVAL;
D O I
10.1016/j.wneu.2019.07.137
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: High-dose bevacizumab delivered via super selective intraarterial cerebral infusion (SIACI) is one promising clinical trial combination for patients with glioblastoma (GBM). Although both continuous intravenous and intra-arterial administration of bevacizumab, and rechallenge with intravenous bevacizumab, have demonstrated improved survival, this is the first description of rechallenging GBM with SIACI of bevacizumab. CASE DESCRIPTION: We report a case of a 43-year-old woman with recurrent GBM who had received treatment from 3 clinical trials, including a rechallenge with SIACI of bevacizumab. First, she enrolled into a phase I/II trial for patients newly diagnosed with GBM (NCT01811498) and received 3 doses of SIACI bevacizumab over 180 days in addition to standard of care chemotherapy and radiation. Following progression, as indicated on her magnetic resonance imaging scan, she consented for a separate clinical trial for her disease and received 2 cycles of temozolomide with an investigational agent. The patient was removed from the study on tumor progression. Subsequently, she was rechallenged with SIACI of bevacizumab via a third clinical trial (NCT01269853) and then completed 3 intravenous infusions. After completing the third trial, her magnetic resonance imaging scan demonstrated improvement based on Response Assessment In Neuro-Oncology criteria. CONCLUSIONS: This is the first report to highlight the effect of rechallenging a patient with SIACI of bevacizumab following disease progression after initial bevacizumab treatment and subsequent alternate clinical trial failure. There is a need to conduct further clinical trials to evaluate the benefits of rechallenge with SIACI versus intravenous bevacizumab for GBM and further explore theories of bevacizumab resistance.
引用
收藏
页码:234 / 241
页数:8
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