Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences, 2-5-1, Shikata-cho, Okayama 700-8558, Japan.
Innovation Center Okayama for Nanobio-targeted Therapy, 2-5-1, Shikata-cho, Okayama 700-8558, Japan.
Future Oncol. 2020 Feb;16(6):151-159. doi: 10.2217/fon-2019-0743. Epub 2020 Jan 24.
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.
恶性脑胶质瘤是人类最常见的脑癌之一,具有很强的破坏性。在各种人类癌症中,永生细胞/ Dickkopf-3(REIC/Dkk-3)表达减少。最近,我们开发了一种新型的第二代腺病毒载体,可表达 REIC/Dkk-3(Ad-SGE-REIC),并揭示了其抗脑胶质瘤的功效。本研究是一项由研究者发起的、单臂、前瞻性、非随机、非对照、开放性、单中心临床试验,在日本冈山大学医院进行。主要终点是剂量限制性毒性和不良事件的发生率。次要终点是客观缓解率和免疫评估。使用 Ad-SGE-REIC 将有助于改善恶性脑肿瘤患者的预后。