4.5 Review

Oncolytic viruses: clinical applications as vectors for the treatment of malignant gliomas

期刊

JOURNAL OF NEURO-ONCOLOGY
卷 65, 期 3, 页码 203-226

出版社

SPRINGER
DOI: 10.1023/B:NEON.0000003651.97832.6c

关键词

clinical trials; G207; gene therapy; HSV 1716; malignant glioma; newcastle disease virus; oncolytic; ONYX-015 adenovirus; poliovirus replicon; reovirus; vaccinia

资金

  1. NCI NIH HHS [P50 CA097247, P01 CA71933] Funding Source: Medline
  2. NINDS NIH HHS [1K08NSO1942] Funding Source: Medline
  3. NATIONAL CANCER INSTITUTE [P01CA071933, P50CA097247] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [K08NS001942] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Gene therapy using viral vectors for the treatment of primary brain tumors has proven to be a promising novel treatment modality. Much effort in the past has been placed in utilizing replication-defective viruses to this end but they have shown many disadvantages. Much recent attention has been focused on the potential of replication-competent viruses to discriminatingly target, replicate within, and destroy tumor cells via oncolysis, leaving adjacent post-mitotic neurons unharmed. The engineered tumor-selective herpes simplex-1 virus (HSV-1) mutants G207 and HSV1716 have completed Phase I investigations in the treatment of recurrent high-grade glioma. The results of these clinical trials are reviewed here. This review also aims to examine the manipulation and development of other viruses for the treatment of malignant glioma, including Newcastle disease virus, reovirus, poliovirus, vaccinia virus, and adenoviruses, in particular the adenovirus mutant ONYX-015.

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