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[西方国家癌症临床试验协作组的基础设施]

[Infrastructure of cancer clinical trial cooperative groups in western countries].

作者信息

Fukuda H

机构信息

Japan Clinical Oncology Group Data Center, National Cancer Center Research Institute.

出版信息

Gan To Kagaku Ryoho. 2000 Jul;27(8):1144-51.

PMID:10945009
Abstract

Efforts for international harmonization have made it clear that Japan is far behind in Western countries in all aspects of infrastructure for clinical trials. The introduction of ICH-GCP, 1998, has promoted the rapid growth of infrastructure for investigational new drug (IND) trials; however, the infrastructure for academic cancer trials has shown no remarkable progress. There is still no governmental regulation, no agency for quality control, and no quality assurance audit system even in government-sponsored trials. The author introduces the quality control systems in cooperative groups in Western countries, such as the Southwest Oncology Group (SWOG), National Surgical Adjuvant Breast and Bowel Project (NSABP) and European Organization for Research and Treatment of Cancer (EORTC), and the quality assurance systems by the National Cancer Institute-Cancer Therapy Evaluation Program (NCI-CTEP). Key activities for quality control in cooperative groups are in-house monitoring, site visit audits, institutional performance evaluations and case report form review by study coordinators. NCI-CTEP oversees cooperative group activities through protocol review, supervision of site visit audits and a monitoring committee. Cancer cooperative groups in Western countries have taken the initiatives in advancement of trial methodology and establishment of clinical trial infrastructure. In order to improve the quality of clinical trials, there is need to invest cancer cooperative groups, thus strengthening the activities for overall clinical trials.

摘要

国际协调的努力已经表明,日本在临床试验基础设施的各个方面都远远落后于西方国家。1998年引入国际人用药品注册技术协调会(ICH)的《药物临床试验质量管理规范》(GCP),推动了研究性新药(IND)试验基础设施的快速发展;然而,学术性癌症试验的基础设施却没有显著进展。即使在政府资助的试验中,仍然没有政府监管、没有质量控制机构、也没有质量保证审核体系。作者介绍了西方国家合作组的质量控制体系,如西南肿瘤协作组(SWOG)、国家乳腺与肠道外科辅助治疗项目(NSABP)和欧洲癌症研究与治疗组织(EORTC),以及美国国立癌症研究所癌症治疗评估项目(NCI-CTEP)的质量保证体系。合作组质量控制的关键活动包括内部监测、实地访查审核、机构绩效评估以及研究协调员对病例报告表的审查。NCI-CTEP通过方案审查、监督实地访查审核以及一个监测委员会来监督合作组的活动。西方国家的癌症合作组在推进试验方法和建立临床试验基础设施方面发挥了带头作用。为了提高临床试验质量,有必要对癌症合作组进行投入,从而加强整体临床试验活动。

相似文献

1
[Infrastructure of cancer clinical trial cooperative groups in western countries].[西方国家癌症临床试验协作组的基础设施]
Gan To Kagaku Ryoho. 2000 Jul;27(8):1144-51.
2
Surgeons: A Future Role in Clinical Trials?外科医生:在临床试验中未来会扮演何种角色?
Oncologist. 1997;2(3):V-VI.
3
Development of cancer cooperative groups in Japan.日本癌症协作组的发展。
Jpn J Clin Oncol. 2010 Sep;40(9):881-90. doi: 10.1093/jjco/hyq135. Epub 2010 Jul 29.
4
[The role of the Japan Clinical Oncology Group].[日本临床肿瘤学会的作用]
Gan To Kagaku Ryoho. 2000 Jul;27(8):1127-32.
5
[Need to establish academic research organization for cancer clinical trial and clinical research system having clinical investigators and study coordinators, with special reference to promotion of medical and life science research policy].[需要建立癌症临床试验的学术研究组织以及拥有临床研究人员和研究协调员的临床研究体系,特别提及医学与生命科学研究政策的推进]
Gan To Kagaku Ryoho. 1999 Jan;26(2 Suppl):235-46.
6
[Post launch studies].[上市后研究]
Gan To Kagaku Ryoho. 2002 Nov;29(11):2037-48.
7
Adapting clinical trials networks to promote cancer prevention and control research.调整临床试验网络以促进癌症预防与控制研究。
Cancer. 2006 Jan 1;106(1):180-7. doi: 10.1002/cncr.21548.
8
[Improving the infrastructure for clinical trials in Japan].[改善日本的临床试验基础设施]
Gan To Kagaku Ryoho. 1999 Jan;26(2 Suppl):225-30.
9
Centralized medical monitoring in phase III clinical trials: the National Surgical Adjuvant Breast and Bowel Project (NSABP) experience.III期临床试验中的集中医学监测:国家外科辅助乳腺和肠道项目(NSABP)的经验
Clin Trials. 2006;3(5):478-85. doi: 10.1177/1740774506070747.
10
[Globalization of clinical trials].[临床试验的全球化]
Gan To Kagaku Ryoho. 2003 Apr;30(4):555-65.

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Development of clinical trials in a cooperative group setting: the eastern cooperative oncology group.协作组环境下临床试验的发展:东部肿瘤协作组
Clin Cancer Res. 2008 Jun 1;14(11):3427-33. doi: 10.1158/1078-0432.CCR-07-5060.