• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

TZT-1027 的 I 期研究,一种新型合成的 dolastatin 10 衍生物和微管聚合抑制剂,每周给晚期实体瘤患者使用 3 周。

Phase I study of TZT-1027, a novel synthetic dolastatin 10 derivative and inhibitor of tubulin polymerization, given weekly to advanced solid tumor patients for 3 weeks.

机构信息

1TZT-1027 Cooperative Study Group, and Division of Thoracic Oncology, Shizuoka Cancer Center, Shimonagakubo 1007 Shunto-gun, Shizuoka, Japan.

出版信息

Cancer Sci. 2009 Feb;100(2):316-21. doi: 10.1111/j.1349-7006.2008.01023.x.

DOI:10.1111/j.1349-7006.2008.01023.x
PMID:19068085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11158325/
Abstract

TZT-1027 is a novel synthetic dolastatin 10 derivative that inhibits tubulin polymerization. A phase I study was conducted to determine the maximum tolerated dose (MTD) of TZT-1027, and to assess its pharmacokinetic profile in Japanese patients with advanced solid tumors following administration of the drug weekly for 3 weeks. Eligible patients had advanced solid tumors that failed to respond to standard therapy or for which no standard therapy was available, and met the following criteria: performance status ≤2 and acceptable organ function. The MTD was defined as the highest dose at which more than two-thirds of the patients experienced grade 4 hematological toxicity or grade 3/4 non-hematological toxicity during weekly TZT-1027 administration for 3 weeks. Forty patients were enrolled in the present study. Twelve doses between 0.3 and 2.1 mg/m2 were evaluated. Grade 4 neutropenia was the principal dose-limiting toxicity (DLT). At a dose of 2.1 mg/m2, two patients developed DLT: one patient developed grade 4 neutropenia, grade 3 myalgia, and grade 4 constipation, and the other one developed grade 4 neutropenia and grade 3 constipation. At a dose level of 1.8 mg/m2, toxicity was acceptable and no DLT was observed. The area under the curve and maximum concentration of TZT-1027 tended to increase linearly with the dose. The DLT observed were neutropenia, myalgia, and constipation, and the MTD was 2.1 mg/m2. The recommended dose for a phase II study was determined to be 1.8 mg/m2 for the drug administered weekly for 3 weeks.

摘要

TZT-1027 是一种新型合成多拉司他汀 10 衍生物,可抑制微管聚合。进行了一项 I 期研究,以确定 TZT-1027 的最大耐受剂量(MTD),并评估其在每周给药 3 周的情况下,日本晚期实体瘤患者的药代动力学特征。符合条件的患者患有晚期实体瘤,这些肿瘤对标准治疗无反应或无标准治疗可用,并且符合以下标准:表现状态≤2 和可接受的器官功能。MTD 定义为在每周 TZT-1027 给药 3 周期间,超过三分之二的患者出现 4 级血液学毒性或 3/4 级非血液学毒性的最高剂量。本研究共纳入 40 例患者。评估了 0.3 至 2.1mg/m2 之间的 12 个剂量。4 级中性粒细胞减少症是主要剂量限制毒性(DLT)。在 2.1mg/m2 剂量时,两名患者发生 DLT:一名患者出现 4 级中性粒细胞减少症、3 级肌痛和 4 级便秘,另一名患者出现 4 级中性粒细胞减少症和 3 级便秘。在 1.8mg/m2 剂量水平时,毒性可接受,未观察到 DLT。TZT-1027 的曲线下面积和最大浓度与剂量呈线性增加趋势。观察到的 DLT 为中性粒细胞减少症、肌痛和便秘,MTD 为 2.1mg/m2。确定每周给药 3 周的药物的 II 期研究推荐剂量为 1.8mg/m2。

相似文献

1
Phase I study of TZT-1027, a novel synthetic dolastatin 10 derivative and inhibitor of tubulin polymerization, given weekly to advanced solid tumor patients for 3 weeks.TZT-1027 的 I 期研究,一种新型合成的 dolastatin 10 衍生物和微管聚合抑制剂,每周给晚期实体瘤患者使用 3 周。
Cancer Sci. 2009 Feb;100(2):316-21. doi: 10.1111/j.1349-7006.2008.01023.x.
2
Phase I study of TZT-1027, a novel synthetic dolastatin 10 derivative and inhibitor of tubulin polymerization, which was administered to patients with advanced solid tumors on days 1 and 8 in 3-week courses.TZT-1027是一种新型合成多拉司他汀10衍生物和微管蛋白聚合抑制剂,在3周疗程的第1天和第8天给予晚期实体瘤患者进行I期研究。
Cancer Chemother Pharmacol. 2007 Jul;60(2):285-93. doi: 10.1007/s00280-006-0382-7. Epub 2006 Nov 30.
3
Phase I and pharmacokinetic study of TZT-1027, a novel synthetic dolastatin 10 derivative, administered as a 1-hour intravenous infusion every 3 weeks in patients with advanced refractory cancer.TZT-1027(一种新型合成多拉司他汀10衍生物)每3周进行1小时静脉输注给药,用于晚期难治性癌症患者的I期和药代动力学研究。
Ann Oncol. 2004 Apr;15(4):671-9. doi: 10.1093/annonc/mdh141.
4
Phase I study of TZT-1027, a novel synthetic dolastatin 10 derivative, for the treatment of patients with non-small cell lung cancer.新型合成多拉司他汀10衍生物TZT-1027用于治疗非小细胞肺癌患者的I期研究。
Cancer Chemother Pharmacol. 2008 Jun;62(1):173-80. doi: 10.1007/s00280-007-0665-7. Epub 2008 Jan 23.
5
Phase I and pharmacokinetic study of the dolastatin 10 analogue TZT-1027, given on days 1 and 8 of a 3-week cycle in patients with advanced solid tumors.在晚期实体瘤患者中,对多拉司他汀10类似物TZT-1027进行的I期和药代动力学研究,给药方案为每3周周期的第1天和第8天给药。
Clin Cancer Res. 2005 May 15;11(10):3806-13. doi: 10.1158/1078-0432.CCR-04-1937.
6
A phase I study of intravenous TZT-1027 administered on day 1 and day 8 of a three-weekly cycle in combination with carboplatin given on day 1 alone in patients with advanced solid tumours.一项针对晚期实体瘤患者的I期研究,在每三周一个周期的第1天和第8天静脉注射TZT-1027,并仅在第1天给予卡铂。
Ann Oncol. 2006 Aug;17(8):1313-9. doi: 10.1093/annonc/mdl097. Epub 2006 May 25.
7
Phase I trial of dolastatin-10 (NSC 376128) in patients with advanced solid tumors.多西他赛(NSC 376128)用于晚期实体瘤患者的I期试验。
Clin Cancer Res. 1999 Mar;5(3):525-31.
8
Characterization of the interaction of TZT-1027, a potent antitumor agent, with tubulin.强效抗肿瘤药物TZT-1027与微管蛋白相互作用的表征
Jpn J Cancer Res. 2000 Jul;91(7):737-47. doi: 10.1111/j.1349-7006.2000.tb01007.x.
9
Phase I study of paclitaxel (taxol) and pegylated liposomal doxorubicin (caelyx) administered every 2 weeks in patients with advanced solid tumors.在晚期实体瘤患者中每2周给予紫杉醇(泰素)和聚乙二醇化脂质体阿霉素(凯素灵)的I期研究。
Oncology. 2002;62(3):216-22. doi: 10.1159/000059568.
10
Phase I and pharmacokinetic study of the dolastatin-15 analogue tasidotin (ILX651) administered intravenously on days 1, 3, and 5 every 3 weeks in patients with advanced solid tumors.多西他赛-15类似物塔西多汀(ILX651)每3周在第1、3和5天静脉给药,用于晚期实体瘤患者的I期和药代动力学研究。
Clin Cancer Res. 2005 Nov 1;11(21):7825-33. doi: 10.1158/1078-0432.CCR-05-0058.

引用本文的文献

1
Marine Antitumor Peptide Dolastatin 10: Biological Activity, Structural Modification and Synthetic Chemistry.海洋抗肿瘤肽 Dolastatin 10:生物活性、结构修饰和合成化学。
Mar Drugs. 2021 Jun 24;19(7):363. doi: 10.3390/md19070363.
2
Recent Advances in Small Peptides of Marine Origin in Cancer Therapy.海洋源小肽在癌症治疗中的最新进展
Mar Drugs. 2021 Feb 19;19(2):115. doi: 10.3390/md19020115.
3
Novel Azetidine-Containing TZT-1027 Analogues as Antitumor Agents.含氮杂环丁烷的新型TZT-1027类似物作为抗肿瘤药物
Mar Drugs. 2016 Apr 28;14(5):85. doi: 10.3390/md14050085.
4
Antibody drug-conjugates targeting the tumor vasculature: Current and future developments.靶向肿瘤血管的抗体药物偶联物:现状与未来发展
MAbs. 2009 May-Jun;1(3):247-53. doi: 10.4161/mabs.1.3.8515.

本文引用的文献

1
The novel microtubule-interfering agent TZT-1027 enhances the anticancer effect of radiation in vitro and in vivo.新型微管干扰剂TZT-1027在体外和体内均可增强辐射的抗癌效果。
Br J Cancer. 2007 May 21;96(10):1532-9. doi: 10.1038/sj.bjc.6603769. Epub 2007 May 1.
2
Tumor-specific antivascular effect of TZT-1027 (Soblidotin) elucidated by magnetic resonance imaging and confocal laser scanning microscopy.通过磁共振成像和共聚焦激光扫描显微镜阐明TZT-1027(索布利多汀)的肿瘤特异性抗血管生成作用。
Cancer Sci. 2007 Apr;98(4):598-604. doi: 10.1111/j.1349-7006.2007.00418.x. Epub 2007 Jan 31.
3
Phase I study of TZT-1027, a novel synthetic dolastatin 10 derivative and inhibitor of tubulin polymerization, which was administered to patients with advanced solid tumors on days 1 and 8 in 3-week courses.TZT-1027是一种新型合成多拉司他汀10衍生物和微管蛋白聚合抑制剂,在3周疗程的第1天和第8天给予晚期实体瘤患者进行I期研究。
Cancer Chemother Pharmacol. 2007 Jul;60(2):285-93. doi: 10.1007/s00280-006-0382-7. Epub 2006 Nov 30.
4
Antivascular effects of TZT-1027 (Soblidotin) on murine Colon26 adenocarcinoma.TZT-1027(索布力多汀)对小鼠结肠26腺癌的抗血管生成作用。
Cancer Sci. 2006 Dec;97(12):1410-6. doi: 10.1111/j.1349-7006.2006.00330.x. Epub 2006 Sep 25.
5
Phase I and pharmacokinetic study of the dolastatin-15 analogue tasidotin (ILX651) administered intravenously on days 1, 3, and 5 every 3 weeks in patients with advanced solid tumors.多西他赛-15类似物塔西多汀(ILX651)每3周在第1、3和5天静脉给药,用于晚期实体瘤患者的I期和药代动力学研究。
Clin Cancer Res. 2005 Nov 1;11(21):7825-33. doi: 10.1158/1078-0432.CCR-05-0058.
6
A phase I study of the dolastatin-15 analogue tasidotin (ILX651) administered intravenously daily for 5 consecutive days every 3 weeks in patients with advanced solid tumors.一项关于多拉司他汀 -15 类似物他昔多丁(ILX651)的 I 期研究,该药物用于晚期实体瘤患者,每 3 周连续 5 天每日静脉给药。
Clin Cancer Res. 2005 Nov 1;11(21):7807-16. doi: 10.1158/1078-0432.CCR-05-0909.
7
Phase I and pharmacokinetic study of the dolastatin 10 analogue TZT-1027, given on days 1 and 8 of a 3-week cycle in patients with advanced solid tumors.在晚期实体瘤患者中,对多拉司他汀10类似物TZT-1027进行的I期和药代动力学研究,给药方案为每3周周期的第1天和第8天给药。
Clin Cancer Res. 2005 May 15;11(10):3806-13. doi: 10.1158/1078-0432.CCR-04-1937.
8
TZT-1027 elucidates antitumor activity through direct cytotoxicity and selective blockade of blood supply.TZT-1027通过直接细胞毒性和选择性阻断血液供应来阐明其抗肿瘤活性。
Anticancer Res. 2004 Jul-Aug;24(4):2201-8.
9
Antitumor activity of TZT-1027 (Soblidotin) against vascular endothelial growth factor-secreting human lung cancer in vivo.TZT-1027(索布利朵汀)对分泌血管内皮生长因子的人肺癌的体内抗肿瘤活性。
Cancer Sci. 2003 Sep;94(9):826-33. doi: 10.1111/j.1349-7006.2003.tb01526.x.
10
An antimicrotubule agent, TZT-1027, does not induce neuropathologic alterations which are detected after administration of vincristine or paclitaxel in animal models.一种抗微管药物TZT-1027不会诱发在动物模型中给予长春新碱或紫杉醇后所检测到的神经病理改变。
Toxicol Lett. 2001 Apr 30;121(2):97-106. doi: 10.1016/s0378-4274(01)00327-7.