scholarly journals Evaluation of PTGS2 Expression, PIK3CA Mutation, Aspirin Use and Colon Cancer Survival in a Population-Based Cohort Study

2017 ◽  
Vol 8 (4) ◽  
pp. e91 ◽  
Author(s):  
Ronan T Gray ◽  
Marie M Cantwell ◽  
Helen G Coleman ◽  
Maurice B Loughrey ◽  
Peter Bankhead ◽  
...  
2017 ◽  
Vol 152 (5) ◽  
pp. S1023
Author(s):  
Ronan T. Gray ◽  
Marie M. Cantwell ◽  
Helen G. Coleman ◽  
Maurice B. Loughrey ◽  
Peter Bankhead ◽  
...  

2017 ◽  
Vol 116 (12) ◽  
pp. 1652-1659 ◽  
Author(s):  
Ronan T Gray ◽  
Maurice B Loughrey ◽  
Peter Bankhead ◽  
Chris R Cardwell ◽  
Stephen McQuaid ◽  
...  

2017 ◽  
Vol 152 (5) ◽  
pp. S1023-S1024
Author(s):  
Ronan T. Gray ◽  
Maurice B. Loughrey ◽  
Peter Bankhead ◽  
Chris Cardwell ◽  
Stephen McQuaid ◽  
...  

2020 ◽  
Vol 7 (1) ◽  
pp. e000413
Author(s):  
Kasper Adelborg ◽  
Dóra Körmendiné Farkas ◽  
Jens Sundbøll ◽  
Lidia Schapira ◽  
Suzanne Tamang ◽  
...  

ObjectiveWe examined the risk of primary gastrointestinal cancers in women with breast cancer and compared this risk with that of the general population.DesignUsing population-based Danish registries, we conducted a cohort study of women with incident non-metastatic breast cancer (1990–2017). We computed cumulative cancer incidences and standardised incidence ratios (SIRs).ResultsAmong 84 972 patients with breast cancer, we observed 2340 gastrointestinal cancers. After 20 years of follow-up, the cumulative incidence of gastrointestinal cancers was 4%, driven mainly by colon cancers. Only risk of stomach cancer was continually increased beyond 1 year following breast cancer. The SIR for colon cancer was neutral during 2–5 years of follow-up and approximately 1.2-fold increased thereafter. For cancer of the oesophagus, the SIR was increased only during 6–10 years. There was a weak association with pancreas cancer beyond 10 years. Between 1990–2006 and 2007–2017, the 1–10 years SIR estimate decreased and reached unity for upper gastrointestinal cancers (oesophagus, stomach, and small intestine). For lower gastrointestinal cancers (colon, rectum, and anal canal), the SIR estimate was increased only after 2007. No temporal effects were observed for the remaining gastrointestinal cancers. Treatment effects were negligible.ConclusionBreast cancer survivors were at increased risk of oesophagus and stomach cancer, but only before 2007. The risk of colon cancer was increased, but only after 2007.


HPB ◽  
2018 ◽  
Vol 20 ◽  
pp. S533
Author(s):  
J. Kirkegård ◽  
M. Ladekarl ◽  
C.W. Fristrup ◽  
C. Palnæs-Hansen ◽  
M. Sall ◽  
...  

PLoS ONE ◽  
2018 ◽  
Vol 13 (8) ◽  
pp. e0202486 ◽  
Author(s):  
Jakob Kirkegård ◽  
Morten Ladekarl ◽  
Claus Wilki Fristrup ◽  
Carsten Palnæs Hansen ◽  
Mogens Sall ◽  
...  

2018 ◽  
Vol 42 (10) ◽  
pp. 1797-1803 ◽  
Author(s):  
Britt W. Jensen ◽  
Lise G. Bjerregaard ◽  
Lars Ängquist ◽  
Ismail Gögenur ◽  
Andrew G. Renehan ◽  
...  

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e16067-e16067
Author(s):  
Sanjay Hinduja ◽  
Mir Ali ◽  
Mohammed SANI Bukari ◽  
Uzair Bashir Chaudhary ◽  
Tanner Mortenson ◽  
...  

e16067 Background: The clinical and mutational profile of Hispanic patients with metastatic colon cancer is not well documented. In this retrospective study, we aim to describe the clinical and mutational profile of Hispanic patients with metastatic colon cancer in central California. Methods: We retrospectively evaluated the clinical and mutational profile of colon cancer at a single institution in Fresno, California from 2010-2019. We selected 136 patients out of which 70 patients self-identified as Hispanic and 66 self-identified as non-Hispanic. We studied clinical parameters and next-generation sequencing via Foundation one testing for these patients. Results: Among Hispanics, there were 43(61%) males and 27(38%) females. The median age at diagnosis was similar in both groups at 57. Right sided colon cancer accounted for 52% of Hispanic patients versus 40% in non-Hispanics. Fifty two percent of Hispanic patients presented with metastatic disease versus 45% in non-Hispanics. The frequency of commonly mutated genes in colon cancer in Hispanics versus non-Hispanics are as follows. KRAS (35.7% vs 37%), NRAS (11% vs 4%) BRAF (8% vs 7%), Her2/neu 0% in both groups. The frequency of other mutations such as TP53, APC, ATM, PTEN, CDKN2A, Myc amplification were also noted to be similar in both groups. PIK3CA mutation was seen in 18.6% of Hispanic patients versus 34% in non-Hispanic population which was statistically significant with a p value = 0.032. Microsatellite instability (MSI) was seen at 3.3% in Hispanics versus 10.6% in non-Hispanics. Tumor mutational burden was similar in both groups. Conclusions: The frequency of actionable mutations was similar in both Hispanic and non-Hispanic patients. Hispanics were noted to have lower PIK3CA and microsatellite instability. Metastatic disease and right sided colon cancer were seen at higher frequency in Hispanic population. Our results were similar to another population-based study which analyzed KRAS mutation with colon cancer patients in Puerto Rico[1]. Larger population based studies would be needed to further assess the differences in this patient population. Ruiz-Candelaria, Y., C. Miranda-Diaz, and R.F. Hunter-Mellado, K-RAS mutation profile in Puerto Rican patients with colorectal cancer: trends from April 2009 to January 2011. Int J Biol Markers, 2013. 28(4): p. e393-7.


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