Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report
Abstract Background Recent advances in molecular oncology have increasingly illuminated the role of germline EGFR mutations in non-small cell lung cancer (NSCLC). This case report presents the presence of a unique familial occurrence of EGFR mutations in patients with NSCLC. Case description A mothe...
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BMC
2025-03-01
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| Series: | BMC Medical Genomics |
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| Online Access: | https://doi.org/10.1186/s12920-025-02113-8 |
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| author | Zacharenia Saridaki Elena Fountzilas Athanasios Alexopoulos Niki Karachaliou |
| author_facet | Zacharenia Saridaki Elena Fountzilas Athanasios Alexopoulos Niki Karachaliou |
| author_sort | Zacharenia Saridaki |
| collection | DOAJ |
| description | Abstract Background Recent advances in molecular oncology have increasingly illuminated the role of germline EGFR mutations in non-small cell lung cancer (NSCLC). This case report presents the presence of a unique familial occurrence of EGFR mutations in patients with NSCLC. Case description A mother and son, both never-smokers of Caucasian ethnicity, were diagnosed with advanced metastatic lung adenocarcinoma. In one patient, tumor molecular analysis by next generation sequencing (NGS) identified two EGFR mutations: the activating mutation c.2573T > G; p.Leu858Arg (p.L858R) in exon 21 of the EGFR gene, and the somatic non-pathogenic mutation c.2612 C > A; p.Ala871Glu (p.A871E) in exon 21 of the EGFR gene. The second patient also harbored the same two EGFR mutations. The patient underwent genetic testing which revealed the germline origin of the A871E mutation. Whether the presence of this mutations was associated with increased predisposition to cancer has yet to be determined. Our case report highlights the need for further exploration of the role of germline mutations, including the A871E mutation, in tumorigenesis and its implications for treatment response and inheritance patterns. Conclusions The investigation and comprehension of the significance of each individual EGFR mutation hold the promise for potential in cancer prevention or early diagnosis within family cohorts and understanding the mechanisms of tumorigenesis in sporadic cases. |
| format | Article |
| id | doaj-art-0edf947acd8a442ca903a5a5ad3b1d06 |
| institution | DOAJ |
| issn | 1755-8794 |
| language | English |
| publishDate | 2025-03-01 |
| publisher | BMC |
| record_format | Article |
| series | BMC Medical Genomics |
| spelling | doaj-art-0edf947acd8a442ca903a5a5ad3b1d062025-08-20T02:56:07ZengBMCBMC Medical Genomics1755-87942025-03-011811510.1186/s12920-025-02113-8Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case reportZacharenia Saridaki0Elena Fountzilas1Athanasios Alexopoulos2Niki Karachaliou3First Oncology Department, Metropolitan HospitalDepartment of Medical Oncology, St. Lukes’s ClinicHYGEIA HospitalZum Gottschalkhof 8Abstract Background Recent advances in molecular oncology have increasingly illuminated the role of germline EGFR mutations in non-small cell lung cancer (NSCLC). This case report presents the presence of a unique familial occurrence of EGFR mutations in patients with NSCLC. Case description A mother and son, both never-smokers of Caucasian ethnicity, were diagnosed with advanced metastatic lung adenocarcinoma. In one patient, tumor molecular analysis by next generation sequencing (NGS) identified two EGFR mutations: the activating mutation c.2573T > G; p.Leu858Arg (p.L858R) in exon 21 of the EGFR gene, and the somatic non-pathogenic mutation c.2612 C > A; p.Ala871Glu (p.A871E) in exon 21 of the EGFR gene. The second patient also harbored the same two EGFR mutations. The patient underwent genetic testing which revealed the germline origin of the A871E mutation. Whether the presence of this mutations was associated with increased predisposition to cancer has yet to be determined. Our case report highlights the need for further exploration of the role of germline mutations, including the A871E mutation, in tumorigenesis and its implications for treatment response and inheritance patterns. Conclusions The investigation and comprehension of the significance of each individual EGFR mutation hold the promise for potential in cancer prevention or early diagnosis within family cohorts and understanding the mechanisms of tumorigenesis in sporadic cases.https://doi.org/10.1186/s12920-025-02113-8Case reportEGFR mutationNon-small cell lung cancerOsimertinib |
| spellingShingle | Zacharenia Saridaki Elena Fountzilas Athanasios Alexopoulos Niki Karachaliou Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report BMC Medical Genomics Case report EGFR mutation Non-small cell lung cancer Osimertinib |
| title | Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report |
| title_full | Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report |
| title_fullStr | Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report |
| title_full_unstemmed | Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report |
| title_short | Inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non-small cell lung cancer: a case report |
| title_sort | inherited rare epidermal growth factor receptor mutation and somatic mutations in patients with non small cell lung cancer a case report |
| topic | Case report EGFR mutation Non-small cell lung cancer Osimertinib |
| url | https://doi.org/10.1186/s12920-025-02113-8 |
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