James Paul, Parry Susan, Arnold Julie, Winship Ingrid
Department of Human Anatomy and Genetics, Oxford University, Oxford, UK.
N Z Med J. 2006 Sep 22;119(1242):U2168.
The optimal management of familial bowel cancer is thought to involve specialised familial cancer units and registries that facilitate a multidisciplinary approach. We studied the impact this approach had on the investigation and management of affected families in our register.
A review of the outcomes of assessment for 25 families was undertaken. These families have completed assessment by the Northern Regional Genetic Service Familial Bowel Cancer Registry because of the possibility of a hereditary bowel cancer syndrome. Details of the cancer history and screening advice known at the time of initial referral to the genetic service, and at the end of assessment, were compared.
Detailed family history revealed 130 cancers, 90 of which were known at referral. Eighty-four cancers were confirmed, of which 73 belonged to the spectrum of cancers associated with hereditary nonpolyposis colorectal cancer (HNPCC). The mean age of diagnosis was 56.3 years. Eight families met the modified Amsterdam Criteria for the diagnosis of HNPCC, compared to four families at the time of referral. Familial hyperplastic polyposis was diagnosed in one family. 164 asymptomatic at-risk first-degree relatives were identified, 48 from families who met the Amsterdam criteria and were thereby recommended to have intensive colonoscopic screening.
Assessment by the Familial Bowel Cancer Registry increased the number of cancers identified in families, thus facilitating a diagnosis of HNPCC in a third of the referred families and a diagnosis of hyperplastic polyposis in one other. Consequently specialised genetic testing and intensive colonoscopic surveillance could be targeted to the asymptomatic first-degree relatives most at risk. Ongoing coordination of colonoscopic surveillance by the registry for those individuals identified to have disease causing mutations or to be at-risk, is anticipated to reduce the number of deaths from colorectal cancer in these families.
家族性肠癌的最佳管理被认为需要专门的家族性癌症单位和登记处,以促进多学科方法。我们研究了这种方法对我们登记册中受影响家庭的调查和管理的影响。
对25个家庭的评估结果进行了回顾。这些家庭因遗传性肠癌综合征的可能性,已由北部地区遗传服务家族性肠癌登记处完成评估。比较了初次转诊至遗传服务机构时以及评估结束时已知的癌症病史和筛查建议的详细信息。
详细的家族史显示有130例癌症,其中90例在转诊时已知。确诊了84例癌症,其中73例属于与遗传性非息肉病性结直肠癌(HNPCC)相关的癌症谱。诊断的平均年龄为56.3岁。有8个家庭符合HNPCC诊断的改良阿姆斯特丹标准,而转诊时为4个家庭。在一个家庭中诊断出家族性增生性息肉病。确定了164名无症状的高危一级亲属,其中48名来自符合阿姆斯特丹标准的家庭,因此被建议进行强化结肠镜筛查。
家族性肠癌登记处的评估增加了家庭中确诊的癌症数量,从而在三分之一的转诊家庭中促成了HNPCC的诊断,并在另一个家庭中诊断出增生性息肉病。因此,专门的基因检测和强化结肠镜监测可以针对风险最高的无症状一级亲属。预计登记处对那些被确定有致病突变或处于风险中的个体进行结肠镜监测的持续协调,将减少这些家庭中结直肠癌的死亡人数。