Balmaña Judith, Sanz Judit, Bonfill Xavier, Casado Alfonso, Rué Montse, Gich Ignasi, Díez Orland, Sabaté Josep M, Baiget Montserrat, Alonso M Carmen
Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Int J Cancer. 2004 Nov 20;112(4):647-52. doi: 10.1002/ijc.20458.
Women with a family history of breast cancer are at increased risk for developing this neoplasm. Starting surveillance more frequently at a younger age than the general population and the possibility of undergoing genetic testing are options for their medical management. We analyzed the benefits and costs of our clinical program in familial breast cancer (FBC) and carried out a cost-effectiveness analysis of such procedure. The benefits and costs of performing genetic counseling and a screening program in FBC based on 143 high-risk families registered in our database between June 1995 and December 2001 were analyzed. A decision tree was constructed to estimate the survival benefit and cost-effectiveness of the clinical genetic counseling program compared with the strategy of not performing any screening protocol. We estimated that the prevalence of a BRCA mutation in an unaffected relative of our high-risk cohort was 10% and that 53% of the mutations are found in the BRCA1 gene. We assigned a 58.5% lifetime risk of breast cancer for a 30-year-old mutation carrier according to the SEER data. The effectiveness of the screening was obtained from our experience and data for estimating survival were derived from other studies with longer follow-up. We used our local payment data to calculate the costs of the program. A mutation in the BRCA1 or BRCA2 genes was identified in 20% of the probands. Seventy primary breast cancer cases were recorded since the onset of the program. Thirty percent of the tumors were diagnosed through the screening program and 71% of them were lymph node-negative compared to 49% of the tumors diagnosed outside the program (p=0.1). The cost-effectiveness ratio of our FBC genetic counseling and screening program was 4,294 euros per life-year gained. The model was sensitive to the prevalence of mutation carriers, the lifetime risk of breast cancer and the effectiveness of the screening. In our setting and according to our model, this analysis suggests that a program of genetic testing and screening for breast cancer in a high-risk population may be cost-effective. These results need to be confirmed as more effective interventions for cancer prevention and screening are being implemented.
有乳腺癌家族史的女性患这种肿瘤的风险增加。与普通人群相比,她们可选择在更年轻时开始更频繁的监测以及进行基因检测。我们分析了我们的家族性乳腺癌(FBC)临床项目的益处和成本,并对该程序进行了成本效益分析。分析了基于1995年6月至2001年12月在我们数据库中登记的143个高危家庭进行FBC基因咨询和筛查项目的益处和成本。构建了一个决策树,以估计临床基因咨询项目与不执行任何筛查方案的策略相比的生存益处和成本效益。我们估计,在我们高危队列的未受影响亲属中,BRCA突变的患病率为10%,且53%的突变存在于BRCA1基因中。根据监测、流行病学和最终结果(SEER)数据,我们为一名30岁的突变携带者赋予了58.5%的终身患乳腺癌风险。筛查的有效性来自我们的经验,估计生存的数据来自其他随访时间更长的研究。我们使用当地支付数据来计算该项目的成本。在20%的先证者中发现了BRCA1或BRCA2基因的突变。自该项目启动以来,记录了70例原发性乳腺癌病例。30%的肿瘤通过筛查项目被诊断出来,其中71%为淋巴结阴性,而在项目外诊断出的肿瘤中这一比例为49%(p = 0.1)。我们的FBC基因咨询和筛查项目的成本效益比为每获得一个生命年4294欧元。该模型对突变携带者的患病率、乳腺癌的终身风险和筛查的有效性敏感。在我们的环境中并根据我们的模型,该分析表明,在高危人群中进行乳腺癌基因检测和筛查项目可能具有成本效益。随着更多有效的癌症预防和筛查干预措施的实施,这些结果需要得到证实。