• 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

MC-键盘:一种整合多级别毒性的靶向治疗和免疫治疗的实用I期试验设计

MC-Keyboard: A Practical Phase I Trial Design for Targeted Therapies and Immunotherapies Integrating Multiple-Grade Toxicities.

作者信息

Jiang Liyun, Yin Zhulin, Yan Fangrong, Yuan Ying

机构信息

Research Center of Biostatistics and Computational Pharmacy, China Pharmaceutical University, Nanjing, China.

Clinical Trials and Statistics Unit, Institute of Cancer Research, London, UK.

出版信息

J Immunother Precis Oncol. 2024 Aug 19;7(3):159-167. doi: 10.36401/JIPO-23-35. eCollection 2024 Aug.

DOI:10.36401/JIPO-23-35
PMID:39219992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11361345/
Abstract

In targeted therapies and immunotherapies, the occurrence of low-grade (e.g., grade 1-2) toxicities (LGT) is common, while dose-limiting toxicities (DLT) are relatively rare. As a result, conventional phase I trial designs, solely based on DLTs and disregarding milder toxicities, are problematic when evaluating these novel therapies. To address this issue, we propose a novel phase I design called a multiple-constraint keyboard (MC-Keyboard) that integrates multiple toxicity constraints, accounting for both DLT and LGT, for precise dose escalation and de-escalation, and identification of the maximum tolerated dose (MTD). As a model-assisted design, an important feature of MC-Keyboard is that its dose-escalation or de-escalation rule can be pretabulated and incorporated into the trial protocol before the initiation of the trial, greatly simplifying its implementation. The simulation study showed that the MC-Keyboard had high accuracy in identifying the MTD and is safer than some existing designs. The MC-Keyboard provides a novel, simple, and safe approach to assessing safety and identifying the MTD for targeted therapies and immunotherapies.

摘要

在靶向治疗和免疫治疗中,低级别(如1 - 2级)毒性反应(LGT)很常见,而剂量限制性毒性反应(DLT)相对少见。因此,传统的仅基于DLT而忽视较轻毒性反应的I期试验设计,在评估这些新型疗法时存在问题。为解决这一问题,我们提出了一种名为多重约束键盘(MC - Keyboard)的新型I期试验设计,该设计整合了多种毒性约束条件,兼顾了DLT和LGT,用于精确的剂量递增和递减,并确定最大耐受剂量(MTD)。作为一种模型辅助设计,MC - Keyboard的一个重要特点是其剂量递增或递减规则可以在试验开始前预先制成表格并纳入试验方案,极大地简化了其实施过程。模拟研究表明,MC - Keyboard在确定MTD方面具有很高的准确性,并且比一些现有设计更安全。MC - Keyboard为评估靶向治疗和免疫治疗的安全性以及确定MTD提供了一种新颖、简单且安全的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/d2cdb86ac0ea/i2590-017X-7-3-159-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/08aaad1b33c4/i2590-017X-7-3-159-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/066d1648a678/i2590-017X-7-3-159-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/8cb31b0030eb/i2590-017X-7-3-159-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/35d8ad4d4cbc/i2590-017X-7-3-159-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/d2cdb86ac0ea/i2590-017X-7-3-159-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/08aaad1b33c4/i2590-017X-7-3-159-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/066d1648a678/i2590-017X-7-3-159-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/8cb31b0030eb/i2590-017X-7-3-159-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/35d8ad4d4cbc/i2590-017X-7-3-159-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e28/11361345/d2cdb86ac0ea/i2590-017X-7-3-159-f05.jpg

相似文献

1
MC-Keyboard: A Practical Phase I Trial Design for Targeted Therapies and Immunotherapies Integrating Multiple-Grade Toxicities.MC-键盘:一种整合多级别毒性的靶向治疗和免疫治疗的实用I期试验设计
J Immunother Precis Oncol. 2024 Aug 19;7(3):159-167. doi: 10.36401/JIPO-23-35. eCollection 2024 Aug.
2
A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method.一种新的实用设计,用于使用适应性连续评估方法在 I 期临床试验中进行剂量递增。
BMC Cancer. 2019 Jun 26;19(1):632. doi: 10.1186/s12885-019-5801-3.
3
Revisiting the definition of dose-limiting toxicities in paediatric oncology phase I clinical trials: An analysis from the Innovative Therapies for Children with Cancer Consortium.重新审视儿科肿瘤I期临床试验中剂量限制毒性的定义:来自儿童癌症创新疗法联盟的分析
Eur J Cancer. 2017 Nov;86:275-284. doi: 10.1016/j.ejca.2017.09.015. Epub 2017 Oct 19.
4
Systematic comparison of the statistical operating characteristics of various Phase I oncology designs.多种I期肿瘤学设计的统计操作特征的系统比较。
Contemp Clin Trials Commun. 2016 Nov 24;5:34-48. doi: 10.1016/j.conctc.2016.11.006. eCollection 2017 Mar.
5
Checkerboard: a Bayesian efficacy and toxicity interval design for phase I/II dose-finding trials.棋盘法:用于I/II期剂量探索试验的贝叶斯疗效和毒性区间设计
J Biopharm Stat. 2020 Nov 1;30(6):1006-1025. doi: 10.1080/10543406.2020.1815033. Epub 2020 Sep 23.
6
Adaptive design for identifying maximum tolerated dose early to accelerate dose-finding trial.用于早期识别最大耐受剂量以加速剂量发现试验的适应性设计。
BMC Med Res Methodol. 2022 Apr 6;22(1):97. doi: 10.1186/s12874-022-01584-y.
7
A software tool for both the maximum tolerated dose and the optimal biological dose finding trials in early phase designs.一种用于早期设计中最大耐受剂量和最佳生物剂量探索试验的软件工具。
Contemp Clin Trials Commun. 2022 Sep 13;30:100990. doi: 10.1016/j.conctc.2022.100990. eCollection 2022 Dec.
8
A novel framework of Bayesian optimal interval design for phase I trials with late-onset toxicities.一种用于具有迟发性毒性的 I 期临床试验的贝叶斯最优区间设计的新框架。
Contemp Clin Trials. 2021 Jun;105:106404. doi: 10.1016/j.cct.2021.106404. Epub 2021 Apr 18.
9
The 3 + 3 design in dose-finding studies with small sample sizes: Pitfalls and possible remedies.在样本量较小的剂量发现研究中使用 3+3 设计:陷阱及可能的补救措施。
Clin Trials. 2024 Jun;21(3):350-357. doi: 10.1177/17407745241240401. Epub 2024 Apr 15.
10
Keyboard: A Novel Bayesian Toxicity Probability Interval Design for Phase I Clinical Trials.《键盘:一种用于I期临床试验的新型贝叶斯毒性概率区间设计》
Clin Cancer Res. 2017 Aug 1;23(15):3994-4003. doi: 10.1158/1078-0432.CCR-17-0220. Epub 2017 May 25.

本文引用的文献

1
Model-Assisted Designs for Early-Phase Clinical Trials: Simplicity Meets Superiority.早期临床试验的模型辅助设计:简单与卓越并存
JCO Precis Oncol. 2019 Oct 24;3. doi: 10.1200/PO.19.00032. eCollection 2019.
2
Keyboard design for phase I drug-combination trials.用于I期药物联合试验的键盘设计。
Contemp Clin Trials. 2020 May;92:105972. doi: 10.1016/j.cct.2020.105972. Epub 2020 Mar 7.
3
Time-to-event model-assisted designs for dose-finding trials with delayed toxicity.时间事件模型辅助设计在延迟毒性剂量发现试验中的应用。
Biostatistics. 2020 Oct 1;21(4):807-824. doi: 10.1093/biostatistics/kxz007.
4
Time-to-Event Bayesian Optimal Interval Design to Accelerate Phase I Trials.基于事件时间的贝叶斯最优区间设计加速 I 期临床试验。
Clin Cancer Res. 2018 Oct 15;24(20):4921-4930. doi: 10.1158/1078-0432.CCR-18-0246. Epub 2018 May 16.
5
Accuracy, Safety, and Reliability of Novel Phase I Trial Designs.新型 I 期临床试验设计的准确性、安全性和可靠性。
Clin Cancer Res. 2018 Sep 15;24(18):4357-4364. doi: 10.1158/1078-0432.CCR-18-0168. Epub 2018 Apr 16.
6
A Bayesian adaptive design for cancer phase I trials using a flexible range of doses.一种用于癌症I期试验的贝叶斯自适应设计,采用灵活的剂量范围。
J Biopharm Stat. 2018;28(3):562-574. doi: 10.1080/10543406.2017.1372774. Epub 2017 Oct 6.
7
ASCEND-8: A Randomized Phase 1 Study of Ceritinib, 450 mg or 600 mg, Taken with a Low-Fat Meal versus 750 mg in Fasted State in Patients with Anaplastic Lymphoma Kinase (ALK)-Rearranged Metastatic Non-Small Cell Lung Cancer (NSCLC).ASCEND-8:一项随机、1 期研究,评估塞瑞替尼 450mg 或 600mg 随低脂餐服用与 750mg 空腹服用在间变性淋巴瘤激酶(ALK)重排转移性非小细胞肺癌(NSCLC)患者中的疗效。
J Thorac Oncol. 2017 Sep;12(9):1357-1367. doi: 10.1016/j.jtho.2017.07.005. Epub 2017 Jul 17.
8
Keyboard: A Novel Bayesian Toxicity Probability Interval Design for Phase I Clinical Trials.《键盘:一种用于I期临床试验的新型贝叶斯毒性概率区间设计》
Clin Cancer Res. 2017 Aug 1;23(15):3994-4003. doi: 10.1158/1078-0432.CCR-17-0220. Epub 2017 May 25.
9
Toxicity management of immunotherapy for patients with metastatic melanoma.免疫治疗转移性黑色素瘤患者的毒性管理。
Ann Transl Med. 2016 Jul;4(14):272. doi: 10.21037/atm.2016.07.10.
10
Pembrolizumab for the treatment of non-small-cell lung cancer.帕博利珠单抗治疗非小细胞肺癌。
N Engl J Med. 2015 May 21;372(21):2018-28. doi: 10.1056/NEJMoa1501824. Epub 2015 Apr 19.