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Updated incidence of EGFR mutation in Middle Eastern patients with non-small cell lung cancer: a 7-year study in a Lebanese institution.

1/5 보강
BMC cancer 📖 저널 OA 94.4% 2026 Vol.26(1)
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
332 patients of which 211 (63.
I · Intervention 중재 / 시술
EGFR mutation testing were included
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Mutational frequencies remain similar, with the highest frequencies being for exon 19 and 21 mutations. [SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s12885-025-14839-w.

Kourie HR, Farhat C, Zouein J, Chebly A, Noujeim F, Riachy M, Dabar G, Harmouche C, Haber B, Bacha ZA, Kattan J, Nasr F, Chahine G, Ghosn M, Trak-Smayra V, ElKarak F, Kesrouani C

📝 환자 설명용 한 줄

[BACKGROUND] This study aims to update the mutational status of EGFR in non-small cell carcinoma (NSCLC), to analyze the spectrum of mutations found, and describe rare mutations in the Lebanese popula

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↓ .bib ↓ .ris
APA Kourie HR, Farhat C, et al. (2026). Updated incidence of EGFR mutation in Middle Eastern patients with non-small cell lung cancer: a 7-year study in a Lebanese institution.. BMC cancer, 26(1). https://doi.org/10.1186/s12885-025-14839-w
MLA Kourie HR, et al.. "Updated incidence of EGFR mutation in Middle Eastern patients with non-small cell lung cancer: a 7-year study in a Lebanese institution.." BMC cancer, vol. 26, no. 1, 2026.
PMID 41656191 ↗

Abstract

[BACKGROUND] This study aims to update the mutational status of EGFR in non-small cell carcinoma (NSCLC), to analyze the spectrum of mutations found, and describe rare mutations in the Lebanese population.

[METHODS] In this retrospective study, patients diagnosed with NSCLC between 2016 and 2023 who underwent EGFR mutation testing were included. EGFR mutations from 2016 to 2019 were analyzed using real-time PCR on the Rotor-Gene Q platform, while those from 2019 to 2023 were analyzed using real-time PCR with the Idylla system.

[RESULTS] 332 patients of which 211 (63.3%) men and 121 (36.7%) women were included. Mean age was 65.7 years. Adenocarcinoma was the main histological subtype. Additionally, 16.3% of patients had an EGFR mutation: 50% had a deletion on exon 19, 37% an L858R mutation, 4% a G719/C/S mutation, 4% a T790M mutation alone, 2% an L861Q mutation alone, and 2% a S768I mutation alone. A statistically significant difference ( < 0.0285) was found between the positivity rates of the two EGFR mutation detection techniques, favoring the Idylla technique.

[CONCLUSION] We confirmed the variation in the incidence of mutated NSCLC between Lebanon and the region. Mutational frequencies remain similar, with the highest frequencies being for exon 19 and 21 mutations.

[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s12885-025-14839-w.

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