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喜树碱糖基化合物的命运:在伊立替康耐药/难治的复发性或转移性结直肠癌患者中进行的 BAY 56-3722(原 BAY 38-3441)二期研究中临床搁置的报告。

The fate of camptothecin glycoconjugate: report of a clinical hold during a phase II study of BAY 56-3722 (formerly BAY 38-3441), in patients with recurrent or metastatic colorectal cancer resistant/refractory to irinotecan.

机构信息

Department of Clinical Oncology, Leiden University Medical Center, Albinusdreef 2, 2300 RC, Leiden, The Netherlands.

出版信息

Invest New Drugs. 2012 Jun;30(3):1208-10. doi: 10.1007/s10637-011-9679-4. Epub 2011 May 6.

Abstract

INTRODUCTION

BAY 56-3722 (formerly BAY 38-3441) is a glycoconjugated campthotecin, which was considered an attractive drug to assess in colorectal cancer (CRC).

PATIENT AND METHODS

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.

RESULTS

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.

DISCUSSION

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.

摘要

简介

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)。

患者和方法

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。

结果

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。

讨论

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。

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