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对年龄小于50岁且有乳腺癌家族史的女性进行筛查。

Screening women aged less than 50 years with a family history of breast cancer.

作者信息

Kollias J, Sibbering D M, Blamey R W, Holland P A, Obuszko Z, Wilson A R, Evans A J, Ellis I O, Elston C W

机构信息

Nottingham City Hospital, U.K.

出版信息

Eur J Cancer. 1998 May;34(6):878-83. doi: 10.1016/s0959-8049(97)00365-1.

Abstract

Family history is an important breast cancer risk factor and is a common reason for referral to specialist breast clinics for consideration of breast screening. The aims of this study were to determine cancer detection rates and prognostic features of breast cancers identified in women aged less than 50 years at increased risk of breast cancer who attend a Family History Breast Screening Clinic (FHC). Between January 1988 and December 1995, 1371 asymptomatic women aged less than 50 years underwent annual clinical breast examination and biennial mammography due to a family history of breast cancer. A total of 29 cancers (23 invasive and 6 in situ) were detected or presented as interval cancer during a mean follow-up of 22 months (range 0-96 months). This gave a relative risk for invasive breast cancer in this high-risk group of 5 when compared with an age-matched female population in the U.K. The cancer screening detection rates were similar to those of women aged 50 years or over undergoing population screening in the NHS Breast Screening Programme (NHSBSP)--FHC prevalent screen 8 per 1000 screening visits versus NHSBSP 6.5 per 1000, FHC incident screen 3.3 per 1000 screening visits versus NHSBSP 3.8 per 1000. A higher proportion of in situ cancers were detected in the FHC screened group compared with cancers identified in symptomatic patients from an age-matched risk group (21% versus 4%). No differences were demonstrated for invasive tumour size, grade or lymph node stage between symptomatic and screened women. The early results of this study suggests that young women at risk of breast cancer due to a family history may benefit from regular breast screening due to the early detection of in situ lesions.

摘要

家族病史是一个重要的乳腺癌风险因素,也是转诊至乳腺专科诊所考虑进行乳腺筛查的常见原因。本研究的目的是确定在家族病史乳腺筛查诊所(FHC)就诊的、患乳腺癌风险增加的50岁以下女性中所发现的乳腺癌的癌症检出率和预后特征。1988年1月至1995年12月期间,1371名50岁以下无症状女性因乳腺癌家族史接受了年度临床乳腺检查和每两年一次的乳房X光检查。在平均22个月(范围0 - 96个月)的随访期间,共检测到29例癌症(23例浸润性癌和6例原位癌)或出现间隔癌。与英国年龄匹配的女性人群相比,该高危组浸润性乳腺癌的相对风险为5。癌症筛查检出率与在国民健康服务乳腺筛查计划(NHSBSP)中接受人群筛查的50岁及以上女性相似——FHC现患筛查每1000次筛查就诊为8例,而NHSBSP为每1000次6.5例;FHC新发病例筛查每1000次筛查就诊为3.3例,而NHSBSP为每1000次3.8例。与年龄匹配的风险组中有症状患者所发现的癌症相比,FHC筛查组中检测到的原位癌比例更高(21%对4%)。有症状女性和筛查女性之间在浸润性肿瘤大小、分级或淋巴结分期方面未显示出差异。本研究的早期结果表明,因家族病史而有乳腺癌风险的年轻女性可能因原位病变的早期发现而从定期乳腺筛查中获益。

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