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A RAND/UCLA appropriateness study of the management of familial gastric cancer.

机译:RAND / UCLA对家族性胃癌治疗的适宜性研究。

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Hereditary diffuse gastric cancer (HDGC) represents a minority of gastric cancer (GC) cases. The goal of this study is to use a RAND/University of California Los Angeles (UCLA) appropriateness methodology to examine indications for genetic referral, CDH1 testing, and consideration of prophylactic total gastrectomy (PTG).A multidisciplinary expert panel of 16 physicians from six countries scored 47 scenarios. Appropriateness of scenarios was scored from 1 (highly inappropriate) to 9 (highly appropriate). Median appropriateness scores (AS) of 1-3 were considered inappropriate, 4-6 uncertain, and 7-9 appropriate. Agreement was reached when 12 of 16 panelists scored the statement similarly. Appropriate scenarios agreed upon were subsequently scored for necessity.The panel felt that patients with family history of diffuse gastric cancer (DGC), lobular breast cancer, or multiple family members with GC should be referred for genetic assessment and multidisciplinary decision-making. The panel felt that it is appropriate for patients with DGC to have CDH1 mutation testing in a family with (1) ≥2 cases of GC, with at least one case of DGC diagnosed before age of 50 years; (2) ≥3 cases of GC diagnosed at any age, one or more of which is DGC; (3) a patient diagnosed with DGC and lobular breast carcinoma; or (4) patients diagnosed with DGC under age of 35 years. The panel felt that PTG should be offered to CDH1 mutation carriers 20 years or older.Identification of genetic mutations in patients at risk for hereditary GC is important, and criteria for testing are suggested.
机译:遗传性弥漫性胃癌(HDGC)代表少数胃癌(GC)病例。这项研究的目的是使用RAND /加利福尼亚大学洛杉矶分校(UCLA)的适当性方法来检查遗传转诊,CDH1检测和预防性全胃切除术(PTG)的适应症。多学科专家小组由来自16位医师的16位医师组成国家得分为47。方案的适当性从1(非常不适当)到9(非常适当)打分。中位适当性得分(AS)1-3被认为是不适当的,4-6不确定,7-9是适当的。当16名小组成员中的12名对此发表了类似的评论时,就达成了共识。专家组认为,有弥漫性胃癌(DGC),小叶性乳腺癌家族史或有多个GC家族成员的患者应转诊进行遗传评估和多学科决策。专家小组认为,对于患有DGC的患者,在(1)≥2例GC的家庭中进行CDH1突变测试是适当的,其中至少一例DGC在50岁之前被诊断; (2)在任何年龄均诊断出≥3例GC,其中DGC为一种或多种; (3)被诊断患有DGC和小叶性乳腺癌的患者;或(4)35岁以下被诊断患有DGC的患者。专家小组认为,应向20岁以上的CDH1突变携带者提供PTG。鉴定具有遗传性GC风险的患者的基因突变很重要,并提出了检测标准。

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