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一项针对日本恶性胶质瘤患者的卡莫司汀植入剂(Gliadel® 晶片)多中心I/II期研究。

A multicenter phase I/II study of the BCNU implant (Gliadel(®) Wafer) for Japanese patients with malignant gliomas.

作者信息

Aoki Tomokazu, Nishikawa Ryo, Sugiyama Kazuhiko, Nonoguchi Naosuke, Kawabata Noriyuki, Mishima Kazuhiko, Adachi Jun-ichi, Kurisu Kaoru, Yamasaki Fumiyuki, Tominaga Teiji, Kumabe Toshihiro, Ueki Keisuke, Higuchi Fumi, Yamamoto Tetsuya, Ishikawa Eiichi, Takeshima Hideo, Yamashita Shinji, Arita Kazunori, Hirano Hirofumi, Yamada Shinobu, Matsutani Masao

机构信息

Department of Neurosurgery, National Hospital Organization Kyoto Medical Center.

出版信息

Neurol Med Chir (Tokyo). 2014;54(4):290-301. doi: 10.2176/nmc.oa2013-0112. Epub 2013 Nov 29.

Abstract

Carmustine (BCNU) implants (Gliadel(®) Wafer, Eisai Inc., New Jersey, USA) for the treatment of malignant gliomas (MGs) were shown to enhance overall survival in comparison to placebo in controlled clinical trials in the United States and Europe. A prospective, multicenter phase I/II study involving Japanese patients with MGs was performed to evaluate the efficacy, safety, and pharmacokinetics of BCNU implants. The study enrolled 16 patients with newly diagnosed MGs and 8 patients with recurrent MGs. After the insertion of BCNU implants (8 sheets maximum, 61.6 mg BCNU) into the removal cavity, various chemotherapies (including temozolomide) and radiotherapies were applied. After placement, overall and progression-free survival rates and whole blood BCNU levels were evaluated. In patients with newly diagnosed MGs, the overall survival rates at 12 months and 24 months were 100.0% and 68.8%, and the progression-free survival rate at 12 months was 62.5%. In patients with recurrent MGs, the progression-free survival rate at 6 months was 37.5%. There were no grade 4 or higher adverse events noted due to BCNU implants, and grade 3 events were observed in 5 of 24 patients (20.8%). Whole blood BCNU levels reached a peak of 19.4 ng/mL approximately 3 hours after insertion, which was lower than 1/600 of the peak BCNU level recorded after intravenous injections. These levels decreased to less than the detection limit (2.00 ng/mL) after 24 hours. The results of this study involving Japanese patients are comparable to those of previous studies in the United States and Europe.

摘要

卡莫司汀(BCNU)植入物(Gliadel®薄片,卫材株式会社,美国新泽西州)用于治疗恶性胶质瘤(MGs),在美国和欧洲的对照临床试验中显示,与安慰剂相比可提高总生存率。开展了一项涉及日本MGs患者的前瞻性多中心I/II期研究,以评估BCNU植入物的疗效、安全性和药代动力学。该研究纳入了16例新诊断的MGs患者和8例复发性MGs患者。在将BCNU植入物(最多8片,61.6 mg BCNU)植入切除腔后,应用了各种化疗(包括替莫唑胺)和放疗。植入后,评估总生存率、无进展生存率和全血BCNU水平。在新诊断的MGs患者中,12个月和24个月时的总生存率分别为100.0%和68.8%,12个月时的无进展生存率为62.5%。在复发性MGs患者中,6个月时的无进展生存率为37.5%。未观察到因BCNU植入物导致的4级或更高级别的不良事件,24例患者中有5例(20.8%)出现3级事件。全血BCNU水平在植入后约3小时达到峰值19.4 ng/mL,低于静脉注射后记录的BCNU峰值水平的1/600。这些水平在24小时后降至检测限(2.00 ng/mL)以下。这项涉及日本患者的研究结果与美国和欧洲先前的研究结果相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a1b/4533485/42ec194bff11/nmc-54-290-g1.jpg

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