* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Emerging Concepts in the Workup of Colorectal Cancer
Survey
Document related concepts
Transcript
Emerging Concepts in the Workup of Colorectal Cancer Short Presentation in Emerging Concepts (SPEC) Mismatch Repair System (MMR) • During replication of each cell’s 3 billion DNA bases, mistakes are introduced • The mismatch repair system (MMR) corrects errors during replication – Functional protein complex composed of four subunits – MLH1, MSH2, MSH6 & PMS2 • Proteins can be detected using IHC • Normal cells express the proteins Defects in the Mismatch Repair System (dMMR) • Sporadic (2/3rd of cases) – Usually the result of methylation (DNA inactivation) of MLH1 gene – Biologic behavior of tumor similar to tumors in patients with inherited mutation • Inherited (1/3rd of cases) – Born with one defective copy of MMR gene – During life, second copy is mutated by chance during DNA replication – Most often MLH1 or MSH2 • Both result in microsatellite instability (MSI) Microsatellite Instability (MSI) • Develops as a result of defects in the mismatch repair system (MMR) • Cells that cannot repair their DNA acquire compounding defects with every cell division • Microsatellites are areas of highly repetitive DNA – Especially prone to errors during DNA replication Colorectal Cancer From: de la Chapelle A. Microsatellite Instability. N Engl J Med. 2003 Jul 17;349(3):209-10. dMMR and MSI • Same underlying biology of the tumor • Test for protein expression (IHC) or genetic abnormalities (MSI) • Significantly better prognosis identified in multiple studies – For stage II – III disease, help decision making for which patients should receive adjuvant chemotherapy EGFR inhibitors (e.g. cetuximab, panitumimab) • Monoclonal antibodies targeted at epidermal growth factor receptors (EGFR) • First line therapy for unresectable, inoperable or metastatic colorectal cancer – Second line therapy after failure of 1st line • No benefit in the presence of a mutation in the KRAS gene! – The targeted pathway is already activated downstream Antibodies approved for colorectal cancer therapy From: Gazdar FA. Cancer Metastasis Rev (2010) KRAS • Mutations in codons 12-13 associated with resistance to EGFR inhibitors – A codon is a set of 3 nucleic acids in a row that code for the amino acid to be inserted when building the protein – Mutations in codons 12-13 cause KRAS to continually signal downstream in the absence of upstream signal, i.e. “switch is stuck in the on position” • Test either the biopsy, primary resection, or metastasis – Mutation occurs early during oncogenesis and persists BRAF • • • • BRAF, like KRAS, is in the EGFR pathway One dominant mutation… V600E Worse prognosis Mixed data whether BRAF mutations confer resistance to EGFR inhibitors, but most believe it does – … the mutation appears to cause downstream signaling in the absence of ligand binding = resistance to anti-EGFR therapy When to test? • Select patients by request or at the time of metastasis? – Testing can take up to 2 weeks – Sequential testing takes longer • Select patients at the time of initial diagnosis or primary resection? – Clinical information and pathologic stage are often incomplete – Does not allow all prognostic values to be incorporated in decision making • All patients at the time of initial diagnosis or primary resection? – – – – More comprehensive diagnostic classification Determination of (in)eligibility for therapy in advance Ideal if not for costs But… there is growing recognition among payers of the need for testing and support for up-front algorithms – and… cost is relatively small in total cost of cancer care Consider Testing • All colorectal adenocarcinomas greater than stage I for: – KRAS Codon 12-13 Mutations – BRAF V600E Mutation – Microsatellite Instability (MSI) Added benefit… detection of inherited cases of colorectal cancer offers opportunity to screen family members. Selected Resources Ross JS. Clinical implementation of KRAS testing in metastatic colorectal carcinoma: the pathologist’s perspective. Arch Pathol Lab Med. 2012;136:1–10. Hutchins G, Southward K, Handley K et al. Value of Mismatch Repair, KRAS, BRAF mutations in predicting recurrence and benefits from chemotherapy In colorectal cancer. J Clin Oncol. 2011;29:1261-1270. National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Colon Cancer v.3.2012. http://www.nccn.org/professionals/physician_gls/pdf/colon.pdf . Accessed August 28, 2013 Karapetis CS, Khambata-Ford S, Jonker DJ, et al. K-ras mutations and benefit from cetuximab in advanced colorectal cancer. N Engl J Med. 2008;359:17571765. Additional Free Resource for CAP Members NOTE: please remove this page before presenting. CAP Member Exclusive: CAP Pathology Resource Guides Focused on a specific hot-topic technology, these comprehensive guides highlights current resources, select journal articles, as well as CAP and non-CAP educational opportunities. And don’t miss the “Insights From Early Adopters” section in each guide to gain perspective from pioneering colleagues. AVAILABLE NOW: • Molecular Pathology (single gene test, small panel) • Genomic Analysis (large panel, exome, genome) Learn more: go to cap.org and type Pathology Resource Guides in the “search” field located at the top of your screen. “An outstanding overview of basic materials, including the technology and links to a number of individuals and centers that can assist.” “Extremely well done, of high practical and educational value.”