Page 250 - EJMO-9-1
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Eurasian Journal of Medicine and
            Oncology
                                                                        EGFR and PIK3CA mutations in lung cancer patients


            by genetic and environmental factors specific to each   We also thank the physicians at the General Laboratory
            population. Despite their low frequency, detecting these   of  Pathological  Anatomy  for  their  contribution  to  the
            genetic alterations is clinically significant and addresses an   anatomopathological examinations.
            unmet medical need, as they can guide patient selection for
            targeted therapies.                                Funding
              The present study provides valuable insights, clearly   None.
            demonstrating the importance of assessing the molecular   Conflict of interest
            profiles of  EGFR and  PIK3CA, and potentially  HER2,
            to better characterize LC tumors for targeted therapy.   All authors declare that they have no competing interests.
            Indeed, 46.7% of patients in our cohort have EGFR and/or
            PIK3CA mutations, making them eligible for associated   Author contributions
            targeted therapies. This finding paves the way for   Conceptualization: Fadila Guessous, Imane Chaoui
            developing a therapeutic protocol tailored to Moroccan   Formal analysis: Hind Dehbi, Souheil Boubia, Mohamed
            NSCLC patients harboring such mutations. However, the   Ridai, Mehdi Karkouri
            study has several limitations, mainly related to the sample   Investigation: Youness El Founini, Sara Hafidi, Imane
            size and the molecular protocol used, which targeted only   Chaoui
            a limited number of specific genes. Well-designed future   Methodology:  Youness El Founini, Mohammed Attaleb,
            studies are needed to investigate patient management   Imane Chaoui
            in real-world settings. Specifically, these studies should:   Writing – original draft: Youness  El Founini, Boutaina
            (i) Expand cohort sizes, (ii) examine the relationship   Addoum, Mohammed El Mzibri, Imane Chaoui
            between  EGFR, PIK3CA, and  HER2  expression with   Writing – review & editing: Boutaina Addoum, Mohammed
            clinicopathological parameters, and (iii) incorporate   El Mzibri, Imane Chaoui
            advanced molecular tools such as next-generation
            sequencing,  which  could  enable  the  simultaneous   Ethics approval and consent to participate
            analysis of a broader panel of genes and detect both   The study was approved by the Ethics Committee of Ibn
            common and rare mutations, overcoming the limitations   Rochd University Hospital in Casablanca on November 16,
            of Sanger sequencing, and (iv) include additional clinical   2021. The ethics code is 01/20.  Written informed consent
            outcomes such as OS and PFS to better predict prognosis.   was obtained from all participants to participate in this
            We believe that these efforts will contribute to a deeper   study.
            understanding of the molecular epidemiology of LC
            in Morocco and support the refinement of treatment   Consent for publication
            options for patients.                              Written informed consent for publication was obtained

            5. Conclusion                                      from all participants, and all identifying information has
                                                               been anonymized to ensure privacy.
            Targeting  oncogenic  driver  mutations  in specific genes,
            including  EGFR, PIK3CA, and  HER2, is a key factor in   Availability of data
            selecting patients who may benefit from personalized   The data supporting our findings are available from the
            medicine. In Morocco, driver mutations in  EGFR and   corresponding author upon reasonable request.
            PIK3CA were  detected  in 41.6% and  8.3% of LC cases,
            respectively, while no mutations were detected in HER2.   References
            Moreover, 46.7% of patients exhibited  EGFR and/or   1.   Zhou Q, Meng X, Sun L,  et al. Efficacy and safety of
            PIK3CA mutations and are therefore eligible for associated   KRASG12C inhibitor IBI351 monotherapy in patients with
            targeted therapies. These findings underscore the urgent   advanced NSCLC: Results from a phase 2 pivotal study.
            need to implement routine genetic profiling and provide   J Thorac Oncol. 2024;19(12):1630-1639.
            access to targeted therapies to improve the management of      doi: 10.1016/j.jtho.2024.08.005
            LC in Morocco.
                                                               2.   Erefai O, Soulaymani A, Mokhtari A, Hami H. Clinical and
            Acknowledgments                                       histopathological  pattern  of  lung  cancer  in  Morocco.  Pan
                                                                  Afr Med J. 2022;42:283.
            The authors would like to express their gratitude to the staff
            of the Department of Thoracic Surgery for their assistance      doi: 10.11604/pamj.2022.42.283.35593
            with patient recruitment and fresh tissue collection.   3.   Colombino M, Paliogiannis P, Cossu A, et al. EGFR, KRAS,


            Volume 9 Issue 1 (2025)                        242                              doi: 10.36922/ejmo.7111
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