• 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

Response to letter re: Ethnic origin in cancer clinical trials: overrated or understated? A comprehensive analysis of cancer clinical trials leading to FDA and EMA approvals between 2020 and 2022.

作者信息

Puhr H C, Winkler E C, Preusser M

机构信息

Division of Oncology, Department of Medicine I, Medical University Vienna, Vienna, Austria.

Section for Translational Medical Ethics, Department of Medical Oncology, National Center for Tumor Diseases, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

ESMO Open. 2025 May;10(5):105063. doi: 10.1016/j.esmoop.2025.105063. Epub 2025 Apr 15.

DOI:10.1016/j.esmoop.2025.105063
PMID:40239365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12020823/
Abstract
摘要

相似文献

1
Response to letter re: Ethnic origin in cancer clinical trials: overrated or understated? A comprehensive analysis of cancer clinical trials leading to FDA and EMA approvals between 2020 and 2022.对关于“癌症临床试验中的种族起源:被高估还是被低估?对2020年至2022年期间导致美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的癌症临床试验的全面分析”的信件的回复
ESMO Open. 2025 May;10(5):105063. doi: 10.1016/j.esmoop.2025.105063. Epub 2025 Apr 15.
2
Letter re: Ethnic origin in cancer clinical trials: overrated or understated?-A comprehensive analysis of cancer clinical trials leading to FDA and EMA approvals between 2020 and 2022.关于:癌症临床试验中的种族起源:被高估还是被低估?——对2020年至2022年期间导致美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的癌症临床试验的综合分析
ESMO Open. 2025 May;10(5):105062. doi: 10.1016/j.esmoop.2025.105062. Epub 2025 Apr 11.
3
Ethnic origin in cancer clinical trials: overrated or understated? A comprehensive analysis of cancer clinical trials leading to FDA and EMA approvals between 2020 and 2022.癌症临床试验中的种族起源:被高估还是被低估?对2020年至2022年间导致美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的癌症临床试验的综合分析。
ESMO Open. 2025 Jan;10(1):104093. doi: 10.1016/j.esmoop.2024.104093. Epub 2025 Jan 3.
4
FDA and EMA Approvals of New Breast Cancer Drugs-A Comparative Regulatory Analysis.美国食品药品监督管理局和欧洲药品管理局对新型乳腺癌药物的批准——一项对比性监管分析
Cancers (Basel). 2020 Feb 13;12(2):437. doi: 10.3390/cancers12020437.
5
Characteristics of professional society oncological drug evaluation in the Netherlands from 2016 to 2020: A retrospective analysis.2016年至2020年荷兰专业协会肿瘤药物评估的特点:一项回顾性分析。
J Cancer Policy. 2025 Jun;44:100578. doi: 10.1016/j.jcpo.2025.100578. Epub 2025 Mar 23.
6
A Framework for the Use and Likelihood of Regulatory Acceptance of Single-Arm Trials.用于监管机构接受单臂试验的可能性和使用的框架。
Ther Innov Regul Sci. 2024 Nov;58(6):1214-1232. doi: 10.1007/s43441-024-00693-8. Epub 2024 Sep 16.
7
Quality of biomarker defined subgroups in FDA approvals of PD-1/PD-L1 inhibitors 2014 to 2020.2014年至2020年FDA批准的PD-1/PD-L1抑制剂中生物标志物定义亚组的质量
Int J Cancer. 2022 Jun 1;150(11):1905-1910. doi: 10.1002/ijc.33968. Epub 2022 Feb 26.
8
Comparison between European Medicines Agency and US Food and Drug Administration in Granting Accelerated Marketing Authorizations for Covid-19 Medicines and their Utilized Regulations.比较欧洲药品管理局和美国食品和药物管理局在授予新冠病毒药物加速营销授权及其使用规定方面的情况。
Ther Innov Regul Sci. 2024 Jan;58(1):79-113. doi: 10.1007/s43441-023-00574-6. Epub 2023 Oct 20.
9
Race and Ethnicity Reporting and Enrollment Disparities in Clinical Trials Leading to FDA Approvals for Breast Cancer Between 2010 and 2020.种族和民族报告以及临床试验中的入组差异对 2010 至 2020 年间 FDA 批准的乳腺癌治疗药物的影响。
Clin Breast Cancer. 2023 Aug;23(6):591-597. doi: 10.1016/j.clbc.2023.05.001. Epub 2023 May 10.
10
Food and Drug Administration approvals in phase 3 Cancer clinical trials.食品和药物管理局批准的 3 期癌症临床试验。
BMC Cancer. 2021 Jun 12;21(1):695. doi: 10.1186/s12885-021-08457-5.

引用本文的文献

1
Letter re: Ethnic origin in cancer clinical trials: overrated or understated?-A comprehensive analysis of cancer clinical trials leading to FDA and EMA approvals between 2020 and 2022.关于:癌症临床试验中的种族起源:被高估还是被低估?——对2020年至2022年期间导致美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的癌症临床试验的综合分析
ESMO Open. 2025 May;10(5):105062. doi: 10.1016/j.esmoop.2025.105062. Epub 2025 Apr 11.

本文引用的文献

1
Race and Ethnicity in Biomedical Research: Changing Course and Improving Accountability.生物医学研究中的种族与族裔:改变方向,增强问责制。
JAMA. 2025 Mar 18;333(11):935-936. doi: 10.1001/jama.2024.28390.
2
Absolute neutrophil count by Duffy status among healthy Black and African American adults.根据达菲血型状态划分的健康黑人和非裔美国人成年人的中性粒细胞绝对计数。
Blood Adv. 2023 Feb 14;7(3):317-320. doi: 10.1182/bloodadvances.2022007679.
3
When non-Whiteness becomes a condition.当非白色成为一种条件。
Blood. 2021 Jan 7;137(1):13-15. doi: 10.1182/blood.2020008600.
4
Increased frequency of the single nucleotide polymorphism of the DARC/ACKR1 gene associated with ethnic neutropenia in a cohort of European patients with chronic idiopathic neutropenia.在一组患有慢性特发性中性粒细胞减少症的欧洲患者中,与种族性中性粒细胞减少相关的DARC/ACKR1基因单核苷酸多态性频率增加。
Am J Hematol. 2020 Jul;95(7):E163-E166. doi: 10.1002/ajh.25813. Epub 2020 Apr 17.
5
Prevalence of neutropenia in the U.S. population: age, sex, smoking status, and ethnic differences.美国人群中性粒细胞减少症的患病率:年龄、性别、吸烟状况及种族差异。
Ann Intern Med. 2007 Apr 3;146(7):486-92. doi: 10.7326/0003-4819-146-7-200704030-00004.
6
Benign ethnic neutropenia: what is a normal absolute neutrophil count?良性种族性中性粒细胞减少症:正常的中性粒细胞绝对值是多少?
J Lab Clin Med. 1999 Jan;133(1):15-22. doi: 10.1053/lc.1999.v133.a94931.