Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.

Hereditary nonpolyposis colorectal cancer (HNPCC), also known as Lynch syndrome, is a common autosomal dominant syndrome characterized by early age at onset, neoplastic lesions, and microsatellite instability (MSI). Because cancers with MSI account for approximately 15% of all colorectal cancers and because of the need for a better understanding of the clinical and histologic manifestations of HNPCC, the National Cancer Institute hosted an international workshop on HNPCC in 1996, which led to the development of the Bethesda Guidelines for the identification of individuals with HNPCC who should be tested for MSI. To consider revision and improvement of the Bethesda Guidelines, another HNPCC workshop was held at the National Cancer Institute in Bethesda, MD, in 2002. In this commentary, we summarize the Workshop presentations on HNPCC and MSI testing; present the issues relating to the performance, sensitivity, and specificity of the Bethesda Guidelines; outline the revised Bethesda Guidelines for identifying individuals at risk for HNPCC; and recommend criteria for MSI testing.

[1]  T. Smyrk,et al.  An update of HNPCC (Lynch syndrome). , 1997, Cancer genetics and cytogenetics.

[2]  M. Loda,et al.  Evaluation of Microsatellite Instability and Updated Version Cited Articles Citing Articles E-mail Alerts Evaluation of Microsatellite Instability and Immunohistochemistry for the Prediction of Germ-line Msh2 and Mlh1 Mutations in Hereditary Nonpolyposis Colon Cancer Families , 2022 .

[3]  M. Miyaki,et al.  Pathogenesis of non-familial colorectal carcinomas with high microsatellite instability , 2000, Journal of clinical pathology.

[4]  D. Evans,et al.  Incidence of hereditary non‐polyposis colorectal cancer in a population‐based study of 1137 consecutive cases of colorectal cancer , 1997, The British journal of surgery.

[5]  C. Boland,et al.  A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines. , 1997, Journal of the National Cancer Institute.

[6]  J. Hardcastle,et al.  Colorectal cancer , 1993, Europe Against Cancer European Commission Series for General Practitioners.

[7]  A. Viel,et al.  Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis , 1999, Gut.

[8]  T. Kunkel,et al.  Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability. , 1994, The Journal of biological chemistry.

[9]  S. Gruber,et al.  Phenotype of Microsatellite Unstable Colorectal Carcinomas: Well‐Differentiated and Focally Mucinous Tumors and the Absence of Dirty Necrosis Correlate With Microsatellite Instability , 2003, The American journal of surgical pathology.

[10]  A. de la Chapelle,et al.  Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction , 2000, International journal of cancer.

[11]  J. Mecklin,et al.  The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) , 1991, Diseases of the colon and rectum.

[12]  Daniel J Sargent,et al.  Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[13]  P. Møller,et al.  MSH2 genomic deletions are a frequent cause of HNPCC , 1998, Nature Genetics.

[14]  K. Hemminki,et al.  Familial colorectal adenocarcinoma and hereditary nonpolyposis colorectal cancer: a nationwide epidemiological study from Sweden , 2001, British Journal of Cancer.

[15]  D. Shibata,et al.  Dietary heterocyclic amines and microsatellite instability in colon adenocarcinomas. , 2001, Carcinogenesis.

[16]  L. Aaltonen,et al.  Population-based molecular detection of hereditary nonpolyposis colorectal cancer. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  D. Glavač,et al.  Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening. , 2001, Cancer genetics and cytogenetics.

[18]  Charis Eng,et al.  Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations inMSH2 and MLH1 , 2000, Journal of medical genetics.

[19]  J. Herman,et al.  Low-level microsatellite instability in most colorectal carcinomas. , 2002, Cancer research.

[20]  A. Ziogas,et al.  Characterization of hereditary nonpolyposis colorectal cancer families from a population-based series of cases. , 2001, Journal of the National Cancer Institute.

[21]  A. de la Chapelle,et al.  Genetics of hereditary colon cancer. , 1995, Annual review of genetics.

[22]  J. Mecklin,et al.  Frequency of hereditary nonpolyposis colorectal cancer , 1995, Diseases of the colon and rectum.

[23]  J. Barrett,et al.  Testing guidelines for hereditary non-polyposis colorectal cancer , 2004, Nature Reviews Cancer.

[24]  S. Neuhausen,et al.  Prognostic implications of BAX and TGFBRII mutations in colon cancers with microsatellite instability , 2002, Genes, chromosomes & cancer.

[25]  James R. Eshleman,et al.  Conversion of diploidy to haploidy , 2000, Nature.

[26]  M. Hendrix,et al.  Application of the National Cancer Institute international criteria for determination of microsatellite instability in ovarian cancer. , 2001, Cancer research.

[27]  David Joseph,et al.  Association of tumour site and sex with survival benefit from adjuvant chemotherapy in colorectal cancer , 2000, The Lancet.

[28]  H. Nagai,et al.  Evaluation of screening strategy for detecting hereditary nonpolyposis colorectal carcinoma , 2002, Cancer.

[29]  A. de la Chapelle,et al.  Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers. , 2000, The American journal of pathology.

[30]  L. Aaltonen,et al.  Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. , 1998, The New England journal of medicine.

[31]  A. S. Warthin HEREDITY WITH REFERENCE TO CARCINOMA: AS SHOWN BY THE STUDY OF THE CASES EXAMINED IN THE PATHOLOGICAL LABORATORY OF THE UNIVERSITY OF MICHIGAN, 1895-1913 , 1913 .

[32]  L. Påhlman,et al.  Microsatellite instability in sporadic colorectal cancer is not an independent prognostic factor , 1999, British Journal of Cancer.

[33]  T. Smyrk,et al.  Tumor‐infiltrating lymphocytes are a marker for microsatellite instability in colorectal carcinoma , 2001, Cancer.

[34]  J. W. Kim,et al.  Expression of hMSH2 and hMLH1 in colorectal carcinomas with microsatellite instability. , 1998, Pathology, research and practice.

[35]  H. Lynch,et al.  Lynch Syndrome: History and Current Status , 2004, Disease markers.

[36]  J. Sheu,et al.  Microsatellite instability in gastric carcinoma with special references to histopathology and cancer stages. , 1995, European journal of cancer.

[37]  G. Thomas,et al.  BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines. , 1997, Cancer research.

[38]  V. Weinberg,et al.  Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing. , 2001, Gastroenterology.

[39]  S Srivastava,et al.  A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. , 1998, Cancer research.

[40]  K. Kinzler,et al.  Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements. , 2002, Cancer research.

[41]  A. Carothers,et al.  Evidence for an age‐related influence of microsatellite instability on colorectal cancer survival , 2002, International journal of cancer.

[42]  V. Weinberg,et al.  Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: high-risk clinic versus population-based registry. , 2002, Gastroenterology.

[43]  Peter Beighton,et al.  de la Chapelle, A. , 1997 .

[44]  R. Kurman,et al.  A dualistic model for endometrial carcinogenesis based on immunohistochemical and molecular genetic analyses. , 1997, Verhandlungen der Deutschen Gesellschaft fur Pathologie.

[45]  B. Leggett,et al.  DNA microsatellite instability in hyperplastic polyps, serrated adenomas, and mixed polyps: a mild mutator pathway for colorectal cancer? , 1999, Journal of clinical pathology.

[46]  F. Gilliland,et al.  Patient and tumor characteristics of colon cancers with microsatellite instability: a population-based study. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[47]  L. Aaltonen,et al.  Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC). , 2001, Cancer research.

[48]  B. Leggett,et al.  Distinction between familial and sporadic forms of colorectal cancer showing DNA microsatellite instability. , 2002, European journal of cancer.

[49]  P. Peltomäki,et al.  Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based study. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[50]  S. Laurberg,et al.  Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients , 2002, Gut.

[51]  A. Chapelle Microsatellite instability phenotype of tumors: genotyping or immunohistochemistry? The jury is still out. , 2002 .

[52]  N. Drouot,et al.  Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments. , 2000, Cancer research.

[53]  G. Petersen,et al.  AGA technical review on hereditary colorectal cancer and genetic testing. , 2001, Gastroenterology.

[54]  P. Peltomäki,et al.  Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer. , 1997, Gastroenterology.

[55]  L. Roncucci,et al.  Identification of hereditary nonpolyposis colorectal cancer in the general population. The 6‐year experience of a population‐based registry , 1993, Cancer.

[56]  J. Kleibeuker,et al.  The risk of brain tumours in hereditary non‐polyposis colorectal cancer (HNPCC) , 1996, International journal of cancer.

[57]  A. Chapelle Testing tumors for microsatellite instability , 1999, European Journal of Human Genetics.

[58]  A. Lindblom,et al.  Microsatellite Instability and hMLH1 and hMSH2 Expression Analysis in Familial and Sporadic Colorectal Cancer , 2001, Laboratory Investigation.

[59]  H T Lynch,et al.  New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. , 1999, Gastroenterology.

[60]  J. Rüschoff,et al.  Diagnostic microsatellite instability: definition and correlation with mismatch repair protein expression. , 1997, Cancer research.

[61]  M. Bianco,et al.  Prevalence of HNPCC in a Series of Consecutive Patients on the First Endoscopic Diagnosis of Colorectal Cancer: A Multicenter Study , 1999, Endoscopy.

[62]  M. Leppert,et al.  The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer. , 2001, Gastroenterology.

[63]  W. Karmaus,et al.  Prospective population‐based study on rotavirus disease in Germany , 2002, Acta paediatrica.

[64]  D. Glavač,et al.  Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria , 2000, Journal of medical genetics.

[65]  H. Lynch,et al.  25 years of HNPCC. , 1994, Anticancer research.

[66]  Daniel J Sargent,et al.  Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer. , 2003, The New England journal of medicine.

[67]  A. Duval,et al.  Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR. , 2002, Gastroenterology.

[68]  S. Zeuzem,et al.  Frequency of the Amsterdam Criteria in a Regional German Cohort of Patients with Colorectal Cancer , 2002, Zeitschrift fur Gastroenterologie.

[69]  A. Umar Lynch Syndrome (HNPCC) and Microsatellite Instability , 2004, Disease markers.