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The role of multi-organ cancer predisposition genes in the risk of inherited and histologically diverse gastric cancer
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Advisor(s)
Abstract(s)
Approximately 10% of cases with gastric cancer (GC) exhibit familial clustering, however, only 1–3% of cases can be explained by two known hereditary syndromes: Hereditary Diffuse Gastric Cancer (HDGC) caused by CDH1 and CTNNA1 pathogenic germline variants; and Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS), caused by germline variants in APC 1B promoter. Familial intestinal gastric cancer (FIGC) has been defined clinically, but it remains mostly genetically unexplained. Likewise, the heritability of mixed histology GC remains to be known. We aimed to estimate the frequency of known cancer predisposition gene variants in GC cases with and without a cancer family history, diverse histological subtypes, and varied age of onset. We evaluated the contribution of pathogenic or likely pathogenic (P/LP) variants in well-established moderate-to-high penetrance multi-organ cancer predisposition genes for GC risk in a large international multi-centre retrospective cohort study involving 750 patients with GC of early-onset or family history of cancer, either by panel sequencing or whole exome sequencing (WES). Panel sequencing was conducted on 328 cases, while WES was performed on the remaining 422. Tumour sequence analyses were performed on samples from 15 patients with P/LP variants. Mutations identified in five index cases were also tested in their relatives. We identified 45 patients (6%) with P/LP variants in: ATM (17 cases), BRCA2 (10 cases), MLH1 (five cases), TP53 (three cases), BRCA1, PALB2, RAD51D, and CHEK2 (two patients each), and RAD51C and PMS2 (one case each), all of which were mutually exclusive. The P/LP variant prevalence was higher in intestinal (9.8%) than in diffuse (4.3%) or mixed GC (4.5%) (p-value = 0.023), without difference per mutated gene by histological subtypes. Only 16 of the 45 patients who carried P/LP variants fulfilled the National Comprehensive Cancer Network genetic testing criteria of at least one cancer predisposition syndrome. Our findings indicate that a broader panel of cancer predisposition genes, beyond CDH1 and CTNNA1, should be included in gene panels to investigate germline variants in patients with GC. This would be especially beneficial when there is a family history of cancer, irrespective of histology subtype, as it would increase the chance of identifying patients who could benefit from risk reduction, targeted treatment, and surveillance of other cancer types.
Description
Keywords
Stomach cancer Gastric cancer Familial aggregation Genetic predisposition Homologous recombination Germline variants
Pedagogical Context
Citation
Approximately 10% of cases with gastric cancer (GC) exhibit familial clustering, however, only 1–3% of cases can be explained by two known hereditary syndromes: Hereditary Diffuse Gastric Cancer (HDGC) caused by CDH1 and CTNNA1 pathogenic germline variants; and Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS), caused by germline variants in APC 1B promoter. Familial intestinal gastric cancer (FIGC) has been defined clinically, but it remains mostly genetically unexplained. Likewise, the heritability of mixed histology GC remains to be known. We aimed to estimate the frequency of known cancer predisposition gene variants in GC cases with and without a cancer family history, diverse histological subtypes, and varied age of onset. We evaluated the contribution of pathogenic or likely pathogenic (P/LP) variants in well-established moderate-to-high penetrance multi-organ cancer predisposition genes for GC risk in a large international multi-centre retrospective cohort study involving 750 patients with GC of early-onset or family history of cancer, either by panel sequencing or whole exome sequencing (WES). Panel sequencing was conducted on 328 cases, while WES was performed on the remaining 422. Tumour sequence analyses were performed on samples from 15 patients with P/LP variants. Mutations identified in five index cases were also tested in their relatives. We identified 45 patients (6%) with P/LP variants in: ATM (17 cases), BRCA2 (10 cases), MLH1 (five cases), TP53 (three cases), BRCA1, PALB2, RAD51D, and CHEK2 (two patients each), and RAD51C and PMS2 (one case each), all of which were mutually exclusive. The P/LP variant prevalence was higher in intestinal (9.8%) than in diffuse (4.3%) or mixed GC (4.5%) (p-value = 0.023), without difference per mutated gene by histological subtypes. Only 16 of the 45 patients who carried P/LP variants fulfilled the National Comprehensive Cancer Network genetic testing criteria of at least one cancer predisposition syndrome. Our findings indicate that a broader panel of cancer predisposition genes, beyond CDH1 and CTNNA1, should be included in gene panels to investigate germline variants in patients with GC. This would be especially beneficial when there is a family history of cancer, irrespective of histology subtype, as it would increase the chance of identifying patients who could benefit from risk reduction, targeted treatment, and surveillance of other cancer types.
Publisher
Elsevier