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Prolonged survival with erlotinib followed by afatinib in a caucasian smoker with metastatic poorly differentiated large cell carcinoma of the lung: a case report

机译:厄洛替尼和阿法替尼在高加索吸烟者中转移低分化肺大细胞癌的白种人吸烟者的生存期延长

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摘要

Activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR; ErbB1) – either exon 19 deletions or exon 21 point mutations – are associated with hypersensitivity to EGFR tyrosine kinase inhibitors (TKIs). EGFR mutations are more frequently found in females, non-smokers, Asians, and patients with adenocarcinoma. We report the case of a 51-year-old Caucasian woman with metastatic NSCLC harboring an EGFR exon 19 deletion although she was a smoker and had a poorly differentiated large cell carcinoma. Following a partial response on 4 months of chemotherapy, the patient progressed and was treated with the reversible EGFR TKI erlotinib for 3 y. The patient then developed resistance to erlotinib and went on to receive the irreversible ErbB Family Blocker afatinib for 1 year, attaining a partial response at 4 months. The impressive survival time attained by our patient highlights the clinical benefit of targeting one or more members of the ErbB Family in patients with disseminated NSCLC and EGFR activating mutations.
机译:表皮生长因子受体(EGFR; ErbB1)的酪氨酸激酶结构域中的激活突变-外显子19缺失或外显子21点突变-与对EGFR酪氨酸激酶抑制剂(TKIs)过敏有关。 EGFR突变在女性,非吸烟者,亚洲人和腺癌患者中更常见。我们报道了一名51岁的白人妇女,其转移性NSCLC携带EGFR外显子19缺失,尽管她是一个吸烟者,并患有低分化大细胞癌。化疗4个月后出现部分缓解后,患者进展并接受了可逆的EGFR TKI厄洛替尼治疗3年。然后,患者对厄洛替尼产生了耐药性,并接受了不可逆转的ErbB家庭阻断剂阿法替尼治疗1年,在4个月时获得了部分缓解。我们的患者获得了令人印象深刻的存活时间,突出了针对具有弥散性NSCLC和EGFR激活突变的患者,针对ErbB家族的一个或多个成员的临床益处。

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