Sporadic Colon Cancer: Mismatch Repair Immunohistochemistry and Microsatellite Instability in Omani Subjects

2008 ◽  
Vol 53 (10) ◽  
pp. 2723-2731 ◽  
Author(s):  
Hassan Ashktorab ◽  
Hassan Brim ◽  
Marwa Al-Riyami ◽  
Anand Date ◽  
Kamla Al-Mawaly ◽  
...  
1998 ◽  
Vol 114 ◽  
pp. A636
Author(s):  
Dong Feng Liu ◽  
William M Grady ◽  
Ashwani Rajput ◽  
Sanford Markowitz ◽  
Joseph Willis

2018 ◽  
Vol 36 (15_suppl) ◽  
pp. e15622-e15622
Author(s):  
Tracy Ann Proverbs-Singh ◽  
John Marshall ◽  
Marian M Varda ◽  
Ibrahim Nakhoul ◽  
Bhavesh Balar ◽  
...  

Surgery ◽  
2016 ◽  
Vol 159 (5) ◽  
pp. 1372-1381 ◽  
Author(s):  
Bo Young Oh ◽  
Jung Wook Huh ◽  
Yoon Ah Park ◽  
Yong Beom Cho ◽  
Seong Hyeon Yun ◽  
...  

Gut ◽  
2008 ◽  
Vol 58 (5) ◽  
pp. 661-667 ◽  
Author(s):  
P T Campbell ◽  
K Curtin ◽  
C M Ulrich ◽  
W S Samowitz ◽  
J Bigler ◽  
...  

Author(s):  
Wei-Shone Chen ◽  
Jeou Yuan Chen ◽  
Jacqueline Ming Liu ◽  
Wen Chang Lin ◽  
Kuang Liang King ◽  
...  

2009 ◽  
Vol 27 (11) ◽  
pp. 1814-1821 ◽  
Author(s):  
Monica M. Bertagnolli ◽  
Donna Niedzwiecki ◽  
Carolyn C. Compton ◽  
Hejin P. Hahn ◽  
Margaret Hall ◽  
...  

Purpose Colon cancers exhibiting DNA mismatch repair (MMR) defects demonstrate distinct clinical and pathologic features, including better prognosis and reduced response to fluorouracil (FU) –based chemotherapy. This prospective study investigated adjuvant chemotherapy containing FU and irinotecan in patients with MMR deficient (MMR-D) colon cancers. Patients and Methods Cancer and Leukemia Group B 89803 randomly assigned 1,264 patients with stage III colon cancer to postoperative weekly bolus FU/leucovorin (LV) or weekly bolus irinotecan, FU, and LV (IFL). The primary end point was overall survival; disease-free survival (DFS) was a secondary end point. Tumor expression of the MMR proteins, MLH1 and MSH2, was determined by immunohistochemistry (IHC). DNA microsatellite instability was also assessed using a panel of mono- and dinucleotide markers. Tumors with MMR defects were those demonstrating loss of MMR protein expression (MMR-D) and/or microsatellite instability high (MSI-H) genotype. Results Of 723 tumor cases examined by genotyping and IHC, 96 (13.3%) were MMR-D/MSI-H. Genotyping results were consistent with IHC in 702 cases (97.1%). IFL-treated patients with MMR-D/MSI-H tumors showed improved 5-year DFS as compared with those with mismatch repair intact tumors (0.76; 95% CI, 0.64 to 0.88 v 0.59; 95% CI, 0.53 to 0.64; P = .03). This relationship was not observed among patients treated with FU/LV. A trend toward longer DFS was observed in IFL-treated patients with MMR-D/MSI-H tumors as compared with those receiving FU/LV (0.57; 95% CI, 0.42 to 0.71 v 0.76; 95% CI, 0.64 to 0.88; P = .07; hazard ratio interaction between tumor status and treatment, 0.51; likelihood ratio P = .117). Conclusion Loss of tumor MMR function may predict improved outcome in patients treated with the IFL regimen as compared with those receiving FU/LV.


2019 ◽  
pp. 1-9 ◽  
Author(s):  
Martin E. Gutierrez ◽  
Kristin S. Price ◽  
Richard B. Lanman ◽  
Rebecca J. Nagy ◽  
Irfan Shah ◽  
...  

PURPOSE Genomic testing is recognized in national guidelines as essential to guide appropriate therapy selection in metastatic colorectal cancer. Previous studies report adherence to testing guidelines is suboptimal, but current testing rates have not been assessed. This study reports testing rates in metastatic colon cancer (mCC) for guideline-recommended biomarkers in a US-based population. MATERIALS AND METHODS A retrospective review of data extracted from electronic medical records was performed to identify patients with pathologically confirmed mCC and describe patterns of guideline-aligned biomarker testing. Data were extracted from the electronic health records of 1,497 patients treated at 23 practices across the United States. Both community and academic centers were represented. RESULTS A total of 1,497 patients with mCC diagnosed between January 1, 2013 and December 31, 2017 were identified. Guideline-aligned biomarker testing rates for RAS, BRAF, and microsatellite instability/mismatch repair deficiency over this study period were 41%, 43%, and 51%, respectively. Patients were more likely to have guideline-aligned testing for RAS and BRAF if they were treated at an academic center, were diagnosed with de novo metastatic disease, and were female. In addition, patients < 65 years of age were more likely to have guideline-aligned RAS testing. Of the 177 patients (12% of cohort) who received anti–epidermal growth factor receptor therapy, only 50 (28%) had complete guideline-aligned biomarker testing. CONCLUSION Despite guideline recommendations and significant therapeutic implications, overall biomarker testing rates in mCC remain suboptimal. Adherence to guideline-recommended biomarker testing would potentially reduce exposure to expensive and ineffective therapies, resulting in improved patient outcomes.


Sign in / Sign up

Export Citation Format

Share Document