Department of Clinical Oncology, Leiden University Medical Center, Albinusdreef 2, 2300 RC, Leiden, The Netherlands.
Invest New Drugs. 2012 Jun;30(3):1208-10. doi: 10.1007/s10637-011-9679-4. Epub 2011 May 6.
BAY 56-3722 (formerly BAY 38-3441) is a glycoconjugated campthotecin, which was considered an attractive drug to assess in colorectal cancer (CRC).
Phase II study design evaluating the antitumor activity of BAY 56-3722 i.v. 320 mg/m(2) daily for 3 days every 3 weeks in patients with recurrent or metastatic inoperable CRC resistant to irinotecan.
Twenty-four patients received the study treatment. Triggered by adverse events in two other studies with this compound the study was put on a clinical hold while the safety data were reviewed for the entire program. After the review Bayer decided to withdraw BAY 56-3722 from all clinical investigations.
We felt it was our obligation to share this interrupted phase II study for two reasons: to report the fate of camptothecin glycoconjugate and to report the unique situation of a clinical hold during a phase II study.
BAY 56-3722(原名为 BAY 38-3441)是一种糖基化喜树碱,被认为是一种有吸引力的药物,可用于评估结直肠癌(CRC)。
这是一项评估静脉注射 BAY 56-3722 (320mg/m2),每日一次,连续 3 天,每 3 周为一周期,用于治疗对伊立替康耐药的复发性或转移性不可切除 CRC 患者的抗肿瘤活性的 II 期研究。
24 例患者接受了该研究治疗。由于其他两项研究中该化合物出现了不良反应,研究被暂停,同时对整个研究项目的安全性数据进行了审查。审查后,拜耳决定停止 BAY 56-3722 的所有临床研究。
我们认为出于两个原因,分享这项中断的 II 期研究是我们的责任:报告喜树碱糖缀合物的结果,并报告在 II 期研究期间临床暂停的独特情况。