Pocurull Anna, Herrera-Pariente Cristina, Carballal Sabela, Llach Joan, Sánchez Ariadna, Carot Laura, Botargues Josep María, Cuatrecasas Miriam, Ocaña Teresa, Balaguer Francesc, Bujanda Luis, Moreira Leticia
Gastroenterology Department, Hospital Clínic de Barcelona, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, 08036 Barcelona, Spain.
Gastroenterology Department, Hospital del Mar, 08003 Barcelona, Spain.
Cancers (Basel). 2021 Jun 23;13(13):3132. doi: 10.3390/cancers13133132.
Gastric adenocarcinoma (GC) is a common tumor with high morbidity and mortality. Only 7% of patients with GC are diagnosed before age 50 (early onset gastric cancer (EOGC)), and their characteristics have been poorly described. We aimed to describe clinical, molecular, and genetic characteristics of EOGC. A total of 309 patients with EOGC were retrospectively studied in four Spanish centers. Personal information, family history, and tumor information were registered. Germinal genetic analysis was performed in patients who met current criteria of a hereditary syndrome at the time of diagnosis. The median age at diagnosis was 44 years. The majority (73.3%) of tumors were diffuse, and 78.3% were diagnosed in an advanced stage. Familial aggregation of GC was present in 18/117 (15.4%) cases, and 5/117 (4.3%) met criteria for familial GC. MMR-IHC was performed in 126/309 (40.7%) tumors: 4/126 (3.1%) had loss of expression in MLH1/PMS2, without an associated germline mutation. Sixteen germline genetic analyses were performed, detecting a pathogenic variant in four (25%) cases: one in , one in , and two in . Most EOGC are diffuse and diagnosed in an advanced stage. In these patients, DNA MMR system deficiency is uncommon. Although familial aggregation was observed in only 15% of cases, a germline mutation was found in 25% of patients tested with clinical criteria. This demonstrates that EOGC has a marked genetic heterogeneity, reinforcing the importance of an accurate genetic counseling and enhancing the emerging use of multigene panels.
胃腺癌(GC)是一种常见肿瘤,发病率和死亡率都很高。只有7%的GC患者在50岁之前被诊断出来(早发性胃癌(EOGC)),而且其特征一直没有得到很好的描述。我们旨在描述EOGC的临床、分子和遗传特征。在西班牙的四个中心对总共309例EOGC患者进行了回顾性研究。记录了个人信息、家族史和肿瘤信息。对诊断时符合遗传性综合征现行标准的患者进行了生殖系基因分析。诊断时的中位年龄为44岁。大多数(73.3%)肿瘤为弥漫性,78.3%在晚期被诊断出来。18/117(15.4%)例存在GC家族聚集现象,5/117(4.3%)例符合家族性GC标准。对126/309(40.7%)个肿瘤进行了错配修复免疫组化(MMR-IHC)检测:4/126(3.1%)在MLH1/PMS2中表达缺失,且无相关的种系突变。进行了16次生殖系基因分析,在4例(25%)中检测到致病变异:1例在 ,1例在 ,2例在 。大多数EOGC是弥漫性的且在晚期被诊断出来。在这些患者中,DNA错配修复系统缺陷并不常见。虽然仅在15%的病例中观察到家族聚集现象,但在根据临床标准进行检测的患者中,25%发现了种系突变。这表明EOGC具有显著的遗传异质性,强化了准确的遗传咨询的重要性,并增强了多基因检测板的新兴应用。