کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6185518 1254381 2013 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Implementation of tumor testing for lynch syndrome in endometrial cancers at a large academic medical center
ترجمه فارسی عنوان
اجرای تست تومور برای سندرم لینچ در سرطان آندومتر در یک مرکز پزشکی دانشگاهی بزرگ
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی زنان، زایمان و بهداشت زنان
چکیده انگلیسی


- There were no differences in age, histology, grade, stage, or BMI in patients with Lynch syndrome versus sporadic tumors.
- Universal screening in endometrial cancers is practical and eliminates the chance for missing eligible cases.
- Lynch syndrome screening in endometrial cancer is successfully implemented with collaboration among genetic counselors, gynecologic oncologists, and pathologists.

ObjectivesLynch syndrome (LS) is a hereditary condition that increases the risk for endometrial and other cancers. Recognizing women at risk for LS based on personal/family history is burdensome and imprecise. Tumor testing using microsatellite instability (MSI) testing and immunohistochemistry (IHC) for mismatch repair protein expression can be an effective strategy for identifying potential LS in patients presenting with colorectal or endometrial cancer. Here we describe our experience implementing a screening program for endometrial cancers.MethodsEndometrial cancers diagnosed ≤ 50 years or those with suspicious personal history or histopathologic features were screened with MSI/IHC, June 2009-June 2011. Criteria were later (July 2011-July 2012) expanded to patients diagnosed < 60 years, or at any age with suspicious features, and finally (after August 2012) universal screening was implemented. Screening techniques began with both MSI and IHC for every tumor, and later converted to IHC for two proteins, and MLH1 promoter methylation analysis when indicated. A genetic counselor contacted patients directly to offer genetic counseling appointments.ResultsTwo hundred and forty-five endometrial cancers (average age, 57 years) were screened. Sixty-two patients (25%) had abnormal results, and 42 patients were referred for genetic counseling. Of the 42 patients, 34 underwent genetic counseling, 28 pursued genetic testing, and 11 were diagnosed with LS. When age and pathology criteria were used, 27 eligible cases were overlooked for screening and 3 cases of LS were found only because a clinician requested screening.ConclusionsUniversal screening of endometrial cancers for LS is practical and successfully implemented with collaboration among genetic counselors, gynecologic oncologists, and pathologists.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gynecologic Oncology - Volume 130, Issue 1, July 2013, Pages 121-126
نویسندگان
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