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Evaluating the Value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma

Overview
Specialty Oncology
Date 2021 Apr 28
PMID 33906293
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Abstract

Background: Despite the significant progress in target therapy for the treatment of metastatic colorectal carcinoma (mCRC), the overall survival isn't satisfactory.

Methods: We assessed the expression of Amphiregulin, PTEN, and P21 in sections from 23 paraffin blocks prepared from 23 patients with left-sided mCRC using immunohistochemistry (IHC). The relationship between their level of expressions, clinicopathological parameters, response to anti-EGFR, and prognosis were analyzed.

Results: High Amphiregulin, PTEN and low P21 expression levels were associated with low tumor grade (p= 0.038 and 0.025 respectively), better response to anti-EGFR treatment (p <0.001), and favorable outcome {progression-free survival (PFS) and overall survival (OS)} (p <0.05). There was a direct relation between Amphiregulin and PTEN expressions (phi coefficient=+0.840), while there was an inverse relation between P21expression and both Amphiregulin (phi coefficient= -0.840) and PTEN expressions (phi coefficient = -1.000), which was statistically significant (P <0.001).

Conclusion: High Amphiregulin and PTEN expression levels and low P21 expression levels were associated with better response to anti-EGFR therapy and improved survival outcome. They might be considered predictive markers of response to anti-EGFR therapy in mCRC.<br /> <br />.

References
1.
Shao Y, Shen Y, Chen T, Xu F, Chen X, Zheng S . The functions and clinical applications of tumor-derived exosomes. Oncotarget. 2016; 7(37):60736-60751. PMC: 5312416. DOI: 10.18632/oncotarget.11177. View

2.
Okada Y, Miyamoto H, Goji T, Takayama T . Biomarkers for predicting the efficacy of anti-epidermal growth factor receptor antibody in the treatment of colorectal cancer. Digestion. 2014; 89(1):18-23. DOI: 10.1159/000356202. View

3.
Khelwatty S, Essapen S, Bagwan I, Green M, Seddon A, Modjtahedi H . The impact of co-expression of wild-type EGFR and its ligands determined by immunohistochemistry for response to treatment with cetuximab in patients with metastatic colorectal cancer. Oncotarget. 2016; 8(5):7666-7677. PMC: 5352351. DOI: 10.18632/oncotarget.13835. View

4.
Sood A, McClain D, Maitra R, Basu-Mallick A, Seetharam R, Kaubisch A . PTEN gene expression and mutations in the PIK3CA gene as predictors of clinical benefit to anti-epidermal growth factor receptor antibody therapy in patients with KRAS wild-type metastatic colorectal cancer. Clin Colorectal Cancer. 2012; 11(2):143-50. PMC: 3350566. DOI: 10.1016/j.clcc.2011.12.001. View

5.
Spano J, Milano G, Vignot S, Khayat D . Potential predictive markers of response to EGFR-targeted therapies in colorectal cancer. Crit Rev Oncol Hematol. 2008; 66(1):21-30. DOI: 10.1016/j.critrevonc.2007.11.005. View