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Preoperative diagnosis of Lynch syndrome with DNA mismatch repair immunohistochemistry on a diagnostic biopsy.
- Source :
-
Diseases of the colon and rectum [Dis Colon Rectum] 2011 Dec; Vol. 54 (12), pp. 1480-7. - Publication Year :
- 2011
-
Abstract
- Background: DNA mismatch repair immunohistochemistry on tumor tissue is a simple, readily available, and cost-effective method of identifying patients with Lynch syndrome in the postoperative setting. The aim of the study was to assess whether the mismatch repair status of a colorectal cancer can be confirmed by mismatch repair immunohistochemistry on preoperative biopsy.<br />Design: Germline positive patients with Lynch syndrome were identified from a prospectively collected Familial Cancer Clinic database. Preoperative colorectal cancer biopsy specimens were obtained from the source pathology provider to generate a cohort of matched preoperative and postoperative specimens. The specimens were sectioned and stained for 4 mismatch repair proteins (MLH1, MSH2, MSH6, PMS2). An age-matched cohort to compare specimens was selected from Bethesda positive but mismatch repair immunohistochemistry negative patients. All slides were reviewed by a single blinded pathologist. The Wilson method was used to calculate a true underlying proportion of patients for whom the preoperative result matched the postoperative test result with a 95% confidence interval.<br />Results: Of 128 germline positive mutation carriers, 40 patients (mean age 41, SD 11.3) had colorectal resections. Thirty-three preoperative specimens were retrievable and were matched with biopsies from 33 controls. The germline mutations included in the study were 8 MLH1, 19 MSH2, 3 MSH6, and 2 PMS2. In patients where germline positive status was known, sensitivity was 100% (95% CI 89.2-100) and specificity was 100% (95% CI 89.2-100). Identical sensitivity and specificity were observed in 33 age-matched patients. The sensitivity of the endoscopic biopsy in predicting germline status was 94.9% (95% CI 80.4-98.3).<br />Conclusion: The mismatch repair disease status of a colorectal cancer can be reliably confirmed by mismatch repair immunohistochemistry on a diagnostic colorectal cancer biopsy sample before definitive surgery. Ascertaining a diagnosis of Lynch syndrome before definitive surgery can influence surgical planning.
- Subjects :
- Adaptor Proteins, Signal Transducing genetics
Adaptor Proteins, Signal Transducing metabolism
Adenosine Triphosphatases genetics
Adenosine Triphosphatases metabolism
Adult
Aged
Biomarkers, Tumor metabolism
Biopsy
Case-Control Studies
Colorectal Neoplasms, Hereditary Nonpolyposis genetics
Colorectal Neoplasms, Hereditary Nonpolyposis metabolism
Colorectal Neoplasms, Hereditary Nonpolyposis surgery
DNA Repair Enzymes genetics
DNA Repair Enzymes metabolism
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Humans
Immunohistochemistry
Middle Aged
Mismatch Repair Endonuclease PMS2
MutL Protein Homolog 1
MutS Homolog 2 Protein genetics
MutS Homolog 2 Protein metabolism
Nuclear Proteins genetics
Nuclear Proteins metabolism
Sensitivity and Specificity
Single-Blind Method
Biomarkers, Tumor genetics
Colon pathology
Colorectal Neoplasms, Hereditary Nonpolyposis pathology
DNA Mismatch Repair genetics
Germ-Line Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1530-0358
- Volume :
- 54
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Diseases of the colon and rectum
- Publication Type :
- Academic Journal
- Accession number :
- 22067175
- Full Text :
- https://doi.org/10.1097/DCR.0b013e318231db1f