Analysis of Molecular Pretreated Tumor Profiles as Predictive Biomarkers of Therapeutic Response and Survival Outcomes after Neoadjuvant Therapy for Rectal Cancer in Moroccan Population

Author:

El Otmani Ihsane123ORCID,El Agy Fatima12ORCID,El Baradai Sanae2,Bouguenouch Laila3,Lahmidani Nada4,El Abkari Mohammed4,Benajah Dafr Allah4,Toughrai Imane5,El Bouhaddouti Hicham5,Mouaqit Ouadii5,Ibn Majdoub Hassani Karim5,Mazaz Khalid5,Benjelloun El Bachir5,Ousadden Abdelmalek5,El Rhazi Karima6,Bouhafa Touria7,Benbrahim Zineb8ORCID,Ouldim Karim3,Ibrahimi Sidi Adil5,Ait Taleb Khalid5,Chbani Laila12

Affiliation:

1. Laboratory of Biomedical and Translational Research, University of Medicine and Pharmacy of Fez, Morocco

2. Laboratory of Anatomic Pathology and Molecular Pathology, University Hospital Hassan II, 30070 Fes, Morocco

3. Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, 30070 Fes, Morocco

4. Department of Gastroenterology, University Hospital Hassan II, 30070 Fes, Morocco

5. Department of General surgery, University Hospital Hassan II, 30070 Fes, Morocco

6. Department of Epidemiology, University of Medicine and Pharmacy, 30070 Fes, Morocco

7. Department of Radiotherapy, University Hospital Hassan II, 30070 Fes, Morocco

8. Department of Oncology, University Hospital Hassan II, 30070 Fes, Morocco

Abstract

Pathologic features depending on tumor response to preoperative chemoradiotherapy are important to determine the outcomes in patients with rectal cancer. Evaluating the potential predictive roles of biomarker expression and their prognostic impact is a promising challenge. We reported here the immunohistochemical staining of a panel marker of mismatch repair protein (MMR), Ki67, HER-2, and p53. Additionally, identification of somatic mutations of KRAS, NRAS, and BRAF genes were performed by direct sequencing and pyrosequencing in pretreated biopsy tissues from 57 patients diagnosed for rectal cancer. Clinical features and pathological criteria for postneoadjuvant treatment surgical resection specimen’s data were collected. Immunohistochemical expression and mutational status were correlated with therapeutic response, overall survival, and disease progression. The mean age of patients was 56 years. Seven (12.3%) out of 57 patients had a complete therapeutic response. Our analysis showed that when using complete therapeutic response (Dworak 4) and incomplete therapeutic response (Dworak 3, 2, and 1) as grouping factor, high p53 expression at the pretreatment biopsy was significantly associated to an incomplete response (p=0.002). For 20 and 2 out of 57, KRAS and NRAS mutations were detected, respectively. The majority of these mutations affected codon 12. KRAS mutations detected at codon 146 (A146T, A146V) was associated with the appearance of recurrence and distant metastasis (p=0.019). A high expression of HER-2 corresponding to score 3+ was observed in 3 pretreatment biopsy specimens. This class was significantly associated with a short relapse-free survival (p=0.002). Furthermore, the high expression of Ki67 was moderately correlated with an older age (p=0.016, r=0.319). In addition, this shows that high p53 expression in the pretreatment biopsy was associated with an incomplete response in surgical resection specimens after neoadjuvant treatment, and a HER-2 score 3+ can be a predictive factor of distant metastasis and local recurrence. Larger, prospective, and more studies are needed.

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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