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Acquired Resistance to Afatinib Mediated by EGFR T790M in Lung Adenocarcinoma Patients Harboring EGFR-KDD: A Case Report and Literature Review.

증례보고 2/5 보강
Current oncology (Toronto, Ont.) 📖 저널 OA 94.3% 2021: 2/2 OA 2022: 9/9 OA 2023: 10/10 OA 2024: 22/22 OA 2025: 104/104 OA 2026: 117/133 OA 2021~2026 2026 Vol.33(4) OA Lung Cancer Treatments and Mutations
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출처
PubMed DOI OpenAlex 마지막 보강 2026-04-30

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: EGFR-KDD who achieved a sustained initial response to afatinib lasting 67 months before developing acquired resistance
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Five of the eleven cases harbored EGFR T790M, yielding a prevalence of 45%, which is similar to that seen in classical EGFR mutations.
OpenAlex 토픽 · Lung Cancer Treatments and Mutations Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis Lung Cancer Diagnosis and Treatment

Liu Q, Lv L, Pang G, Wang P

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📝 환자 설명용 한 줄

Epidermal growth factor receptor (EGFR)-kinase domain duplication (KDD) represents an atypical mutation distinct from classical EGFR mutations in lung adenocarcinoma (LUAD).

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↓ .bib ↓ .ris
APA Qian Liu, Lu Lv, et al. (2026). Acquired Resistance to Afatinib Mediated by EGFR T790M in Lung Adenocarcinoma Patients Harboring EGFR-KDD: A Case Report and Literature Review.. Current oncology (Toronto, Ont.), 33(4). https://doi.org/10.3390/curroncol33040214
MLA Qian Liu, et al.. "Acquired Resistance to Afatinib Mediated by EGFR T790M in Lung Adenocarcinoma Patients Harboring EGFR-KDD: A Case Report and Literature Review.." Current oncology (Toronto, Ont.), vol. 33, no. 4, 2026.
PMID 42041733 ↗

Abstract

Epidermal growth factor receptor (EGFR)-kinase domain duplication (KDD) represents an atypical mutation distinct from classical EGFR mutations in lung adenocarcinoma (LUAD). Although first- and second-generation EGFR-tyrosine kinase inhibitors (TKIs) have demonstrated clinical activity in EGFR-KDD, the mechanisms of acquired resistance in this setting remain poorly characterized. Herein, we present a LUAD patient with EGFR-KDD who achieved a sustained initial response to afatinib lasting 67 months before developing acquired resistance. Re-biopsy with next-generation sequencing (NGS) uncovered EGFR T790M, accompanied by EGFR amplification and EGFR M766T. The patient was switched to firmonertinib, with subsequent tumor regression. We reviewed published EGFR-KDD cases that had both acquired resistance to first- or second-generation EGFR-TKIs and corresponding repeat biopsy findings. Five of the eleven cases harbored EGFR T790M, yielding a prevalence of 45%, which is similar to that seen in classical EGFR mutations. This case suggests that EGFR T790M mediates acquired resistance to first- and second-generation EGFR-TKIs in EGFR-KDD, mirroring the resistance pattern observed in classical EGFR mutations.

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