• 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

建立和运营一家家族性癌症诊所。

Setting up and running a familial cancer clinic.

作者信息

Ponder B A

机构信息

CRC Human Cancer Genetics Research Group, Department of Pathology, Cambridge, UK.

出版信息

Br Med Bull. 1994 Jul;50(3):732-45. doi: 10.1093/oxfordjournals.bmb.a072921.

DOI:10.1093/oxfordjournals.bmb.a072921
PMID:7987652
Abstract

This article is based on the author's own experience of establishing and running a familial cancer clinic over the past 9 years. There are certainly other ways of doing it, depending on the clinical context--resources, involvement of colleagues from other specialities--and each clinic should be adapted to local circumstances. As the familial component of the common cancers such as breast and colorectal cancers is increasingly recognised, and DNA-based predictive testing becomes a possibility, the future demand for genetic advice is likely to increase dramatically. This will almost certainly require a re-appraisal of the way in which familial cancer services are provided, which is discussed in the final section.

摘要

本文基于作者在过去9年中建立和运营一家家族性癌症诊所的亲身经历。当然,根据临床情况——资源、其他专科同事的参与情况——还有其他的做法,每个诊所都应因地制宜。随着乳腺癌和结直肠癌等常见癌症的家族性成分越来越受到认可,基于DNA的预测性检测成为可能,未来对基因咨询的需求可能会大幅增加。几乎可以肯定,这将需要重新评估提供家族性癌症服务的方式,这将在最后一部分进行讨论。

相似文献

1
Setting up and running a familial cancer clinic.建立和运营一家家族性癌症诊所。
Br Med Bull. 1994 Jul;50(3):732-45. doi: 10.1093/oxfordjournals.bmb.a072921.
2
Cancer genetics services in Northern Ireland.北爱尔兰的癌症遗传学服务。
Dis Markers. 1999 Oct;15(1-3):37-40. doi: 10.1155/1999/161754.
3
A multidisciplinary model for cancer care management.
Oncol Nurs Forum. 2006 Jul;33(4):697-700. doi: 10.1188/06.ONF.697-700.
4
Genetic services for familial cancer patients: a survey of National Cancer Institute cancer centers.
J Natl Cancer Inst. 1995 Oct 4;87(19):1446-55. doi: 10.1093/jnci/87.19.1446.
5
Service Delivery Model and Experiences in a Cancer Genetics Clinic for an Underserved Population.为服务不足人群设立的癌症遗传学诊所的服务提供模式与经验
J Health Care Poor Underserved. 2015 Aug;26(3):784-91. doi: 10.1353/hpu.2015.0090.
6
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.美国临床肿瘤学会政策声明更新:癌症易感性基因检测
J Clin Oncol. 2003 Jun 15;21(12):2397-406. doi: 10.1200/JCO.2003.03.189. Epub 2003 Apr 11.
7
Why do women attend familial breast cancer clinics?女性为何前往家族性乳腺癌诊所?
J Med Genet. 2000 Mar;37(3):197-202. doi: 10.1136/jmg.37.3.197.
8
Cancer risk assessment and genetics at the Helen F. Graham Cancer Center: model for personalized medicine and early intervention.海伦·F·格雷厄姆癌症中心的癌症风险评估与遗传学:个性化医疗与早期干预模式
Del Med J. 2006 Sep;78(9):325-32.
9
The need for oncogenetic counselling. Ten years' experience of a regional oncogenetic clinic.肿瘤遗传咨询的必要性。一家地区肿瘤遗传诊所的十年经验。
Acta Oncol. 2004;43(7):637-49. doi: 10.1080/02841860410018520.
10
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.BRCA1/2 和 Lynch 综合征患者缺乏遗传咨询和检测转诊:基于 240134 次就诊和 134652 次基因检测的全国性研究。
Breast Cancer Res Treat. 2013 Aug;141(1):135-44. doi: 10.1007/s10549-013-2669-9. Epub 2013 Aug 24.

引用本文的文献

1
The Role of Online Support, Caregiving, and Gender in Preventative Cancer Genetic Testing Participation: Cross-Sectional Study From a National Study.在线支持、照护及性别在预防性癌症基因检测参与中的作用:一项全国性研究的横断面研究
JMIR Cancer. 2025 Jun 4;11:e67650. doi: 10.2196/67650.
2
Cancer Genetic Counseling-Current Practice and Future Challenges.癌症遗传咨询——当前实践与未来挑战。
Cold Spring Harb Perspect Med. 2020 Jun 1;10(6):a036541. doi: 10.1101/cshperspect.a036541.
3
An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers.
一项针对未受影响的BRCA1和BRCA2突变携带者监测方案的国际调查。
Breast Cancer Res Treat. 2016 Jun;157(2):319-327. doi: 10.1007/s10549-016-3805-0. Epub 2016 Apr 27.
4
The Familial Cancer Program of the Vermont Cancer Center: Development of a Cancer Genetics Program in a Rural Area.佛蒙特癌症中心的家族性癌症项目:农村地区癌症遗传学项目的发展。
J Genet Couns. 1997 Jun;6(2):131-45. doi: 10.1023/A:1025603900839.
5
The Effect of Genetic Counseling on Knowledge and Perceptions Regarding Risks for Breast Cancer.遗传咨询对乳腺癌风险相关知识及认知的影响
J Genet Couns. 1998 Oct;7(5):417-34. doi: 10.1023/A:1022880831996.
6
A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes.英国针对家族性癌症的基因风险咨询服务的随机对照比较:心理社会结果
Br J Cancer. 2004 Aug 31;91(5):884-92. doi: 10.1038/sj.bjc.6602081.
7
Referrals of women with a family history of breast cancer from primary care to cancer genetics services in South East Scotland.在苏格兰东南部,将有乳腺癌家族史的女性从初级保健机构转诊至癌症遗传学服务机构。
Br J Cancer. 2003 Nov 3;89(9):1650-6. doi: 10.1038/sj.bjc.6601348.
8
A descriptive study of UK cancer genetics services: an emerging clinical response to the new genetics.英国癌症遗传学服务的描述性研究:对新遗传学的一种新兴临床应对措施
Br J Cancer. 2001 Jul 20;85(2):166-70. doi: 10.1054/bjoc.2001.1893.
9
High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects.在42个有少量有症状个体的比利时家族中,BRCA1/2种系突变的高频率。
J Med Genet. 1999 Apr;36(4):304-8.
10
The future of breast and ovarian cancer clinics.乳腺癌和卵巢癌诊所的未来。
BMJ. 1995 Dec 16;311(7020):1584-5. doi: 10.1136/bmj.311.7020.1584.