Prognostic Value of HER2 in Metastatic Colorectal Cancer: A Single Institutional Experience | ||
| The Egyptian Journal of Hospital Medicine | ||
| Article 35, Volume 88, Issue 1, July 2022, Pages 2496-2502 PDF (714.42 K) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/ejhm.2022.238378 | ||
| Authors | ||
| Mai Ezz El Din* ; Radwa Abd El-Azeem Yassin; Mohamed Mohamed El Bassiouny; Manal Mohamed El-Mahdy; Mohamed Yassin Mostafa | ||
| Abstract | ||
| Background: HER2 (Human epidermal growth factor receptor 2) activation has been associated with poor prognosis in a number of tumours as breast, gastric and lung cancers, but the prognostic role of HER2 in colorectal cancer (CRC) remains unclear. Objective: The aim of the current work was to detect the incidence and prognostic impact of HER2 overexpression in metastatic CRC patients in relation to clinico-pathologic features and outcome. Patients and Methods: Data of metastatic CRC patients treated from January 2012 to end of December 2016 in a tertiary referral university hospital were collected. Eligible patients had their paraffin block tested for HER2. Results: Clinico-pathologic features of 70 patients were available for analysis. Age ranged 20-73 years, at a median of 39.5 years. Fifty (71.4%) of these cases were left sided. Male to female ratio was 3:4. Mucinous variant was present in 27.1 %( 19 cases). Synchronous metastasis constituted 61.4%. HER2 incidence was found in 8.57% (6 cases). Her2 positivity was significantly associated with a shorter time to progression on both first line of therapy, PFS1 (mPFS1 3 vs. 6 months, p=0.045) and PFS2 (mPFS2 4 vs.6 months, p=0.036). No significant relation to clinico-pathological characteristics or OS were detected. Conclusion: HER2 positivity was not associated with clinico-pathologic features but was related to outcome with a shorter PFS but not OS in metastatic CRC. Further prospective data sets are required to confirm its prognostic role. | ||
| Keywords | ||
| HER2; Metastatic colorectal cancer; Prognostic factor | ||
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