• 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

加权毒性评分:用于在系统癌症治疗随机试验中沟通毒性的简单指标的验证。

The Weighted Toxicity Score: Confirmation of a Simple Metric to Communicate Toxicity in Randomized Trials of Systemic Cancer Therapy.

机构信息

Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Oncologist. 2024 Jan 5;29(1):67-74. doi: 10.1093/oncolo/oyad192.

DOI:10.1093/oncolo/oyad192
PMID:37449664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10769778/
Abstract

INTRODUCTION

FDA's Project Optimus was developed in part to better identify appropriate dose and schedule of cancer therapeutics. The tabular method to summarize patients' maximum toxicity in a clinical trial does not allow for ready comparison to the treatment's benefit. In this manuscript, we apply a simple tool, the weighted toxicity score (WTS), to trials involving lung cancer immunotherapy and chemotherapy, as well as those cited in a recent publication as examples of trials that represent successful reduction of the appropriate dose of anti-cancer agents.

METHODS

PubMed was queried for randomized controlled trials of therapy involving immune checkpoint inhibitors in lung cancer. Trial data from studies highlighting initial success with dose adjustments after FDA approval also were assembled and analyzed according to the WTS procedure described previously, compared to clinical outcomes data.

RESULTS

The WTS provided, with the clinical outcome(s), a data pair that leads to easy interpretation of the expected benefit versus relative toxicity of studies involving immunotherapy or chemoimmunotherapy in lung cancers. The WTS was consistent with the conclusions of the primary studies, helping to quantitate the toxicity difference between treatments in a previously unavailable way.

CONCLUSION

The WTS provides a tool to show the cost in toxicity of therapy in a randomized clinical trial, with applicability to studies involving chemotherapy, immunotherapy, or kinase-directed therapy. Inclusion of a running tally of WTS during conduct of a trial could serve as one means to adjust dosing or to provide feedback during data safety monitoring of a clinical trial.

摘要

简介

FDA 的 Project Optimus 的开发部分是为了更好地确定癌症治疗药物的适当剂量和方案。临床试验中总结患者最大毒性的表格方法不便于与治疗的益处进行直接比较。在本文中,我们应用了一种简单的工具,即加权毒性评分(WTS),来分析涉及肺癌免疫疗法和化疗的试验,以及最近一篇文献中作为成功降低抗癌药物适当剂量的试验示例。

方法

在 PubMed 上检索涉及肺癌免疫检查点抑制剂治疗的随机对照试验。还按照先前描述的 WTS 程序,从强调在 FDA 批准后调整剂量以取得初步成功的研究中收集和分析试验数据,并与临床结果数据进行比较。

结果

WTS 与临床结果(s)一起提供了一个数据对,使人们可以轻松解释涉及肺癌免疫疗法或化疗免疫疗法的研究的预期益处与相对毒性之间的关系。WTS 与主要研究的结论一致,有助于以以前无法获得的方式量化治疗之间的毒性差异。

结论

WTS 提供了一种工具,可以显示随机临床试验中治疗的毒性成本,适用于涉及化疗、免疫疗法或激酶靶向治疗的研究。在试验进行过程中纳入 WTS 的累计分数,可以作为调整剂量的一种手段,或在临床试验的数据安全监测期间提供反馈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/10769778/784ec98ff5cc/oyad192_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/10769778/1be09ef2d246/oyad192_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/10769778/784ec98ff5cc/oyad192_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/10769778/1be09ef2d246/oyad192_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/10769778/784ec98ff5cc/oyad192_fig2.jpg

相似文献

1
The Weighted Toxicity Score: Confirmation of a Simple Metric to Communicate Toxicity in Randomized Trials of Systemic Cancer Therapy.加权毒性评分:用于在系统癌症治疗随机试验中沟通毒性的简单指标的验证。
Oncologist. 2024 Jan 5;29(1):67-74. doi: 10.1093/oncolo/oyad192.
2
A Method to Summarize Toxicity in Cancer Randomized Clinical Trials.一种总结癌症随机临床试验中毒性的方法。
Clin Cancer Res. 2018 Oct 15;24(20):4968-4975. doi: 10.1158/1078-0432.CCR-17-3314. Epub 2018 May 8.
3
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.在流行地区,服用抗叶酸抗疟药物的人群中,叶酸补充剂与疟疾易感性和严重程度的关系。
Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217.
4
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
5
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
6
Oblimersen: Augmerosen, BCL-2 antisense oligonucleotide - Genta, G 3139, GC 3139, oblimersen sodium.奥布利默森:奥古默森,BCL-2反义寡核苷酸——根塔公司,G 3139,GC 3139,奥布利默森钠
Drugs R D. 2007;8(5):321-34. doi: 10.2165/00126839-200708050-00006.
7
The Next Immune-Checkpoint Inhibitors: PD-1/PD-L1 Blockade in Melanoma.下一代免疫检查点抑制剂:黑色素瘤中的PD-1/PD-L1阻断
Clin Ther. 2015 Apr 1;37(4):764-82. doi: 10.1016/j.clinthera.2015.02.018. Epub 2015 Mar 29.
8
A Phase I/II Clinical Trial to evaluate the efficacy of baricitinib to prevent respiratory insufficiency progression in onco-hematological patients affected with COVID19: A structured summary of a study protocol for a randomised controlled trial.一项评估巴瑞替尼预防 COVID19 相关血液肿瘤患者呼吸功能不全进展的疗效的 I/II 期临床试验:一项随机对照试验研究方案的结构化总结。
Trials. 2021 Feb 5;22(1):116. doi: 10.1186/s13063-021-05072-4.
9
Durvalumab in frail and elderly patients with stage four non-small cell lung cancer: Study protocol of the randomized phase II DURATION trial.度伐利尤单抗用于体弱和老年四期非小细胞肺癌患者:随机II期DURATION试验的研究方案
Trials. 2020 Apr 22;21(1):352. doi: 10.1186/s13063-020-04280-8.
10
Immunotherapy for advanced renal cell cancer.晚期肾细胞癌的免疫疗法。
Cochrane Database Syst Rev. 2005 Jan 25(1):CD001425. doi: 10.1002/14651858.CD001425.pub2.

本文引用的文献

1
The Drug-Dosing Conundrum in Oncology - When Less Is More.肿瘤学中的给药难题——少即是多。
N Engl J Med. 2021 Oct 14;385(16):1445-1447. doi: 10.1056/NEJMp2109826. Epub 2021 Oct 9.
2
Evaluating Treatment Tolerability Using the Toxicity Index With Patient-Reported Outcomes Data.使用基于患者报告结局数据的毒性指数评估治疗耐受性。
J Pain Symptom Manage. 2022 Feb;63(2):311-320. doi: 10.1016/j.jpainsymman.2021.07.031. Epub 2021 Aug 8.
3
Adverse event burden in older patients with CLL receiving bendamustine plus rituximab or ibrutinib regimens: Alliance A041202.
接受苯达莫司汀联合利妥昔单抗或伊布替尼方案治疗的老年 CLL 患者的不良事件负担:Alliance A041202。
Leukemia. 2021 Oct;35(10):2854-2861. doi: 10.1038/s41375-021-01342-x. Epub 2021 Jul 17.
4
On the properties of the toxicity index and its statistical efficiency.关于毒性指数的性质及其统计效率
Stat Med. 2021 Mar 15;40(6):1535-1552. doi: 10.1002/sim.8858. Epub 2020 Dec 20.
5
Adverse event load, onset, and maximum grade: A novel method of reporting adverse events in cancer clinical trials.不良事件负荷、发作和最大等级:一种报告癌症临床试验中不良事件的新方法。
Clin Trials. 2021 Feb;18(1):51-60. doi: 10.1177/1740774520959313. Epub 2020 Oct 1.
6
Is the onset of adverse effects of immunotherapy always bad news for the patients…?-certainly not!免疫疗法不良反应的出现对患者来说就总是坏消息吗……?当然不是!
Ann Transl Med. 2019 Mar;7(Suppl 1):S5. doi: 10.21037/atm.2019.01.14.
7
Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042): a randomised, open-label, controlled, phase 3 trial.帕博利珠单抗对比化疗用于未经治疗、PD-L1 表达、局部晚期或转移性非小细胞肺癌(KEYNOTE-042):一项随机、开放标签、对照、III 期临床试验。
Lancet. 2019 May 4;393(10183):1819-1830. doi: 10.1016/S0140-6736(18)32409-7. Epub 2019 Apr 4.
8
First-Line Atezolizumab plus Chemotherapy in Extensive-Stage Small-Cell Lung Cancer.阿替利珠单抗联合化疗一线治疗广泛期小细胞肺癌。
N Engl J Med. 2018 Dec 6;379(23):2220-2229. doi: 10.1056/NEJMoa1809064. Epub 2018 Sep 25.
9
A Method to Summarize Toxicity in Cancer Randomized Clinical Trials.一种总结癌症随机临床试验中毒性的方法。
Clin Cancer Res. 2018 Oct 15;24(20):4968-4975. doi: 10.1158/1078-0432.CCR-17-3314. Epub 2018 May 8.
10
Estimating global treatment toxicity burden from adverse-event data.从不良事件数据估算全球治疗毒性负担。
Cancer. 2018 Feb 15;124(4):858-864. doi: 10.1002/cncr.31107. Epub 2017 Nov 7.