• 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

肌肉浸润性和转移性尿路上皮癌当代临床研究的批判性分析:膀胱癌倡导网络临床试验工作组的报告。

Critical analysis of contemporary clinical research in muscle-invasive and metastatic urothelial cancer: a report from the Bladder Cancer Advocacy Network Clinical Trials Working Group.

机构信息

Mount Sinai School of Medicine, Tisch Cancer Institute, New York, NY 10029, USA.

出版信息

Cancer. 2013 Jun 1;119(11):1994-8. doi: 10.1002/cncr.27973. Epub 2013 Mar 1.

DOI:10.1002/cncr.27973
PMID:23456777
Abstract

BACKGROUND

There have been no improvements in the treatment of metastatic urothelial cancer in the past several decades. A census of contemporary clinical research in this disease was performed to identify potential barriers and opportunities.

METHODS

These authors performed a search for clinical trials exploring interventions in muscle-invasive and metastatic urothelial cancer, using the ClinicalTrials.gov registry. Data extracted from the registry included title, recruitment status, interventions, sponsor, phase, enrollment, study design, and study sites.

RESULTS

Among 120 eligible trials exploring interventions in muscle-invasive and metastatic urothelial cancer, 73% were phase 2 and 73% were nonrandomized. The majority (63%) involved treatment in the metastatic disease state. The median planned enrollment size per trial was 45 patients (interquartile range, 47 patients). The majority of trials (55%) involved ≤ 3 study sites. Trials most commonly explored interventions in the first-line metastatic (30%) or second-line metastatic (37%) settings. Targeted therapeutics were studied in 58% of the trials. Among 56 trials that completed enrollment, the median time to complete accrual was 50 months (range, 10-109 months), and these trials enrolled a median of 40 patients per trial (interquartile range, 44 patients).

CONCLUSIONS

The majority of contemporary clinical trials in muscle-invasive and metastatic urothelial cancer are small, nonrandomized, phase 2 trials involving 1 to 3 study sites. Enhanced communication and collaboration among the urothelial cancer community, and other stakeholders, is needed to facilitate the design and conduct of trials capable of expediting progress in this disease.

摘要

背景

在过去几十年中,转移性尿路上皮癌的治疗没有任何进展。为了确定潜在的障碍和机会,对该疾病的当代临床研究进行了普查。

方法

作者使用 ClinicalTrials.gov 注册中心对探索肌层浸润性和转移性尿路上皮癌干预措施的临床试验进行了搜索。从注册中心提取的数据包括标题、招募状态、干预措施、赞助商、阶段、入组、研究设计和研究地点。

结果

在 120 项探索肌层浸润性和转移性尿路上皮癌干预措施的合格试验中,73%为 2 期试验,73%为非随机试验。大多数(63%)涉及转移性疾病状态的治疗。每个试验的计划入组人数中位数为 45 例(四分位间距,47 例)。大多数试验(55%)涉及≤3 个研究地点。试验最常探索一线转移性(30%)或二线转移性(37%)环境中的干预措施。靶向治疗在 58%的试验中进行了研究。在完成入组的 56 项试验中,完成入组的中位数时间为 50 个月(范围,10-109 个月),这些试验每试验中位数入组 40 例(四分位间距,44 例)。

结论

肌层浸润性和转移性尿路上皮癌的当代临床试验大多数为小型、非随机、2 期试验,涉及 1 至 3 个研究地点。需要加强尿路上皮癌社区以及其他利益相关者之间的沟通与协作,以促进能够加速该疾病进展的试验的设计和开展。

相似文献

1
Critical analysis of contemporary clinical research in muscle-invasive and metastatic urothelial cancer: a report from the Bladder Cancer Advocacy Network Clinical Trials Working Group.肌肉浸润性和转移性尿路上皮癌当代临床研究的批判性分析:膀胱癌倡导网络临床试验工作组的报告。
Cancer. 2013 Jun 1;119(11):1994-8. doi: 10.1002/cncr.27973. Epub 2013 Mar 1.
2
Nomogram for predicting survival in patients with unresectable and/or metastatic urothelial cancer who are treated with cisplatin-based chemotherapy.用于预测接受以顺铂为基础的化疗的不可切除和/或转移性尿路上皮癌患者生存情况的列线图。
Cancer. 2013 Aug 15;119(16):3012-9. doi: 10.1002/cncr.28146. Epub 2013 May 29.
3
Relationship between 6- and 9-month progression-free survival and overall survival in patients with metastatic urothelial cancer treated with first-line cisplatin-based chemotherapy.一线顺铂类化疗治疗转移性尿路上皮癌患者的 6 个月和 9 个月无进展生存期与总生存期之间的关系。
Cancer. 2013 Aug 15;119(16):3020-6. doi: 10.1002/cncr.28145. Epub 2013 May 29.
4
Management of patients with muscle-invasive and metastatic bladder cancer.肌层浸润性和转移性膀胱癌患者的管理
Oncology (Williston Park). 2005 Sep;19(10):1333-42; discussion 1342, 1347, 1350 passim.
5
The effect of cystectomy, and perioperative methotrexate, vinblastine, doxorubicin and cisplatin chemotherapy on the risk and pattern of relapse in patients with muscle invasive bladder cancer.膀胱切除术以及围手术期使用甲氨蝶呤、长春花碱、阿霉素和顺铂化疗对肌层浸润性膀胱癌患者复发风险及复发模式的影响。
J Urol. 2000 May;163(5):1413-8.
6
Urothelial cancers: using biology to improve outcomes.尿路上皮癌:利用生物学改善预后。
Expert Rev Anticancer Ther. 2012 Jan;12(1):87-98. doi: 10.1586/era.11.195.
7
Adjuvant chemotherapy for invasive urothelial cancer: experience with a methotrexate, vincristine, cisplatin, cyclophosphamide, adriamycin and bleomycin (MVP-CAB) regimen: a preliminary report.浸润性尿路上皮癌的辅助化疗:甲氨蝶呤、长春新碱、顺铂、环磷酰胺、阿霉素和博来霉素(MVP-CAB)方案的经验:初步报告
Jpn J Clin Oncol. 1993 Oct;23(5):291-8.
8
[Chemotherapy in the treatment of advanced urothelial tumors].[化疗在晚期尿路上皮肿瘤治疗中的应用]
Urologe A. 1991 Jan;30(1):33-44.
9
Bladder cancer clinical trials.膀胱癌临床试验。
Urol Oncol. 2005 Jul-Aug;23(4):275-9. doi: 10.1016/j.urolonc.2005.05.005.
10
Adjuvant chemotherapy for deep muscle-invasive transitional cell bladder carcinoma - a practice guideline.肌层浸润性移行细胞膀胱癌的辅助化疗——实践指南
Can J Urol. 2002 Oct;9(5):1625-33.

引用本文的文献

1
m6A Methylation-Mediated Stabilization of LINC01106 Suppresses Bladder Cancer Progression by Regulating the miR-3148/DAB1 Axis.m6A甲基化介导的LINC01106稳定通过调控miR-3148/DAB1轴抑制膀胱癌进展。
Biomedicines. 2024 Jan 5;12(1):114. doi: 10.3390/biomedicines12010114.
2
LINC01106 post-transcriptionally regulates ELK3 and HOXD8 to promote bladder cancer progression.LINC01106 通过转录后调控 ELK3 和 HOXD8 促进膀胱癌进展。
Cell Death Dis. 2020 Dec 12;11(12):1063. doi: 10.1038/s41419-020-03236-9.
3
Long non-coding RNA ARAP1-AS1 promotes the progression of bladder cancer by regulating miR-4735-3p/NOTCH2 axis.
长链非编码 RNA ARAP1-AS1 通过调控 miR-4735-3p/NOTCH2 轴促进膀胱癌的进展。
Cancer Biol Ther. 2019;20(4):552-561. doi: 10.1080/15384047.2018.1538613. Epub 2018 Nov 7.
4
Long non-coding RNA HNF1A-AS1 promotes proliferation and suppresses apoptosis of bladder cancer cells through upregulating Bcl-2.长链非编码RNA HNF1A-AS1通过上调Bcl-2促进膀胱癌细胞增殖并抑制其凋亡。
Oncotarget. 2017 Sep 8;8(44):76656-76665. doi: 10.18632/oncotarget.20795. eCollection 2017 Sep 29.
5
Society for Immunotherapy of Cancer consensus statement on immunotherapy for the treatment of bladder carcinoma.癌症免疫治疗学会共识声明:免疫疗法治疗膀胱癌。
J Immunother Cancer. 2017 Aug 15;5(1):68. doi: 10.1186/s40425-017-0271-0.
6
Oxaliplatin, 5-fluorouracil and leucovorin (FOLFOX) as second-line therapy for patients with advanced urothelial cancer.奥沙利铂、5-氟尿嘧啶和亚叶酸钙(FOLFOX)作为晚期尿路上皮癌患者的二线治疗方案。
Oncotarget. 2016 Sep 6;7(36):58579-58585. doi: 10.18632/oncotarget.10463.
7
Elevating the Horizon: Emerging Molecular and Genomic Targets in the Treatment of Advanced Urothelial Carcinoma.提升视野:晚期尿路上皮癌治疗中新兴的分子和基因组靶点
Clin Genitourin Cancer. 2015 Oct;13(5):410-20. doi: 10.1016/j.clgc.2015.02.009. Epub 2015 Mar 5.
8
Summary of the 8th Annual Bladder Cancer Think Tank: Collaborating to move research forward.第八届年度膀胱癌智库会议总结:携手推动研究进展
Urol Oncol. 2015 Feb;33(2):53-64. doi: 10.1016/j.urolonc.2014.06.013. Epub 2014 Jul 25.