Wannhoff Andreas, Werner Simone, Tao Sha, Brenner Hermann, Gotthardt Daniel N
Department of Internal Medicine IV, University Hospital Heidelberg, Heidelberg, Germany.
Division of Clinical Epidemiology and Aging Research (C070), German Cancer Research Center (DKFZ), Heidelberg, Germany.
J Gastrointest Oncol. 2022 Aug;13(4):1711-1721. doi: 10.21037/jgo-22-310.
Serum levels of Carbohydrate antigen CA19-9 are determined by the genotype of fucosyltransferases 2 and 3. To validate, possibly modify, and improve a grouping algorithm based on these genotypes.
CA19-9 levels genotypes and of fucosyltransferase 2 and 3 were analyzed in cancer-free and colorectal cancer patients. Patients were assigned to groups with low (group A), intermediate (B), or high (C) CA19-9 biosynthetic activity based on a previously developed grouping algorithm based on genotype of fucosyltransferases 2 and 3.
Three hundred thirty-eight patients were included (n=177 cancer-free). Of cancer-free patients 7.9%, 75.7%, and 16.4% were assigned to groups A, B, and C, respectively. In colorectal cancer patients it 7.5%, 77.0%, and 15.5%, respectively. There were significant differences between median CA19-9 levels in the three groups (P<0.001) in both cohorts. The T59G single-nucleotid polymorphism in fucosyltransferase 3 had a significant influence on CA19-9 levels in cancer-free group B patients, which led to establishment of subgroups B1 and B2. However, no difference in CA19-9 levels between these subgroups was found in colorectal cancer patients. A receiver-operating characteristic showed similar areas under the curve for original group B as well as for subgroups B1 and B2.
The grouping algorithm based on genotype of fucosyltransferases 2 and 3, which defines groups with distinct CA19-9 serum levels, was validated in cancer-free patients and in colorectal cancer patients. No clinically relevant improvement to the grouping algorithm was identified.
血清碳水化合物抗原CA19-9水平由岩藻糖基转移酶2和3的基因型决定。旨在验证、可能修改并改进基于这些基因型的分组算法。
对无癌患者和结直肠癌患者的CA19-9水平、岩藻糖基转移酶2和3的基因型进行分析。根据先前基于岩藻糖基转移酶2和3基因型开发的分组算法,将患者分为CA19-9生物合成活性低(A组)、中等(B组)或高(C组)的组。
共纳入338例患者(n = 177例无癌患者)。无癌患者中,分别有7.9%、75.7%和16.4%被分配到A组、B组和C组。在结直肠癌患者中,这一比例分别为7.5%、77.0%和15.5%。在两个队列中,三组的CA19-9水平中位数之间均存在显著差异(P < 0.001)。岩藻糖基转移酶3中的T59G单核苷酸多态性对无癌B组患者的CA19-9水平有显著影响,从而建立了B1和B2亚组。然而,在结直肠癌患者中,这些亚组之间的CA19-9水平没有差异。受试者工作特征曲线显示,原始B组以及B1和B2亚组的曲线下面积相似。
基于岩藻糖基转移酶2和3基因型的分组算法在无癌患者和结直肠癌患者中得到验证,该算法定义了具有不同CA19-9血清水平的组。未发现该分组算法有临床相关的改进。