1.Screening for Lynch syndrome using risk assessment criteria in patients with ovarian cancer.
Takashi TAKEDA ; Kosuke TSUJI ; Kouji BANNO ; Megumi YANOKURA ; Yusuke KOBAYASHI ; Eiichiro TOMINAGA ; Daisuke AOKI
Journal of Gynecologic Oncology 2018;29(3):e29-
OBJECTIVE: Lynch syndrome is a cancer predisposition syndrome caused by germline mutation of DNA mismatch repair (MMR) genes. Lynch syndrome only causes about 0.4% of cases of ovarian cancer, which suggests that universal screening may not be cost-efficient. However, the frequency of Lynch syndrome in ovarian cancer is unclear in the Asian population. The goal of the study was to investigate a screening strategy using family history. METHODS: The subjects were 129 patients with ovarian cancer. Clinical and family history were collected using a self-administered questionnaire, and Society of Gynecologic Oncology (SGO) criteria 2007 and PREMM5 were used for risk assessment. Microsatellite instability, immunohistochemistry, and methylation of MMR genes were analyzed. RESULTS: Of the 129 cases, 25 (19.4%) met the SGO criteria, and 4 of these 25 had MSI-high and MMR deficiency. Two cases had loss of MSH2 and MSH6, indicating MSH2 mutation, and the other two had loss of MLH1 and PMS2, including one without MLH1 methylation indicating MLH1 mutation. These results show that screening using family history can detect Lynch syndrome in 12.0% (3/25) of ovarian cancer cases. The 3 cases were positive for PREMM5, but negative for Amsterdam II criteria and revised Bethesda guidelines. Genetic testing in one case with MSH2 and MSH6 deficiency confirmed the diagnosis of Lynch syndrome with MSH2 mutation. CONCLUSION: This is the first study of screening for Lynch syndrome in ovarian cancer using clinical and family history in an Asian population. This approach may be effective for diagnosis in these patients.
Asian Continental Ancestry Group
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Colorectal Neoplasms, Hereditary Nonpolyposis*
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Diagnosis
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DNA Mismatch Repair
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Genetic Testing
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Germ-Line Mutation
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Humans
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Immunohistochemistry
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Mass Screening*
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Medical History Taking
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Methylation
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Microsatellite Instability
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Ovarian Neoplasms*
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Risk Assessment*