Convection-enhanced delivery of immunomodulatory therapy for high-grade glioma

被引:12
|
作者
Sperring, Colin P. [1 ,3 ]
Argenziano, Michael G. [1 ]
Savage, William M. [1 ]
Teasley, Damian E. [1 ]
Upadhyayula, Pavan S. [1 ]
Winans, Nathan J. [1 ]
Canoll, Peter [2 ]
Bruce, Jeffrey N. [1 ]
机构
[1] Columbia Univ, Irving Med Ctr, NY Presbyterian Hosp, Dept Neurol Surg, New York, NY USA
[2] Columbia Univ, Irving Med Ctr, NY Presbyterian Hosp, Dept Pathol & Cell Biol, New York, NY USA
[3] 710 W 168th St,Room 434, New York, NY 10032 USA
关键词
convection-enhanced delivery; drug delivery; glioma; immunotherapy; RECURRENT MALIGNANT GLIOMAS; IMMUNOGENIC CELL-DEATH; GROWTH-FACTOR-BETA; DRUG-DELIVERY; GENE-THERAPY; THYMIDINE KINASE; INTERFERON-GAMMA; PHASE-I; GLIOBLASTOMA-MULTIFORME; HUMAN INTERLEUKIN-12;
D O I
10.1093/noajnl/vdad044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis for glioblastoma has remained poor despite multimodal standard of care treatment, including temozolomide, radiation, and surgical resection. Further, the addition of immunotherapies, while promising in a number of other solid tumors, has overwhelmingly failed in the treatment of gliomas, in part due to the immunosuppressive microenvironment and poor drug penetrance to the brain. Local delivery of immunomodulatory therapies circumvents some of these challenges and has led to long-term remission in select patients. Many of these approaches utilize convection-enhanced delivery (CED) for immunological drug delivery, allowing high doses to be delivered directly to the brain parenchyma, avoiding systemic toxicity. Here, we review the literature encompassing immunotherapies delivered via CED-from preclinical model systems to clinical trials-and explore how their unique combination elicits an antitumor response by the immune system, decreases toxicity, and improves survival among select high-grade glioma patients.
引用
收藏
页数:12
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