| Literature DB >> 31973596 |
Kazuhiko Kurozumi1, Kentaro Fujii1, Yosuke Shimazu1, Yusuke Tomita1, Tatsuya Sasaki1, Takao Yasuhara1, Tomohito Hishikawa1, Masahiro Kameda1, Hiromi Kumon2, Isao Date1.
Abstract
Malignant glioma is one of the most common brain cancers in humans, which is very devastating. The expression of Reduced Expression in Immortalized Cells/Dickkopf-3 (REIC/Dkk-3) is decreased in various human cancers. Lately, we have developed a novel second-generation adenoviral vector that expresses REIC/Dkk-3 (Ad-SGE-REIC) and revealed its antiglioma efficacy. The present investigator-initiated clinical trial is a single-arm, prospective, nonrandomized, noncomparative, open-label, single-center trial performed at Okayama University Hospital, Okayama, Japan. The primary end points are dose-limiting toxicities and the incidence of adverse events. The secondary end points are the objective response rate and immunological assessment. Use of Ad-SGE-REIC will help to improve the prognosis of patients with malignant brain tumors.Entities:
Keywords: DKK3; gene therapy; malignant glioma; prognosis; safety
Year: 2020 PMID: 31973596 DOI: 10.2217/fon-2019-0743
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404