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老年罕见表皮生长因子受体突变阳性肺腺癌患者接受阿法替尼治疗的长期疗效。

Long-term response to afatinib in an elderly patient with uncommon epidermal growth factor receptor mutation-positive lung adenocarcinoma.

机构信息

Department of Respiratory Medicine, Hakodate Goryoukaku Hospital, Hakodate-shi, Japan.

Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo-shi, Japan.

出版信息

Thorac Cancer. 2021 Mar;12(6):989-992. doi: 10.1111/1759-7714.13869. Epub 2021 Feb 3.

Abstract

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors are the standard treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. Uncommon mutations, excluding exon 19 deletions and exon 21 L858R, comprise 7%-23% of EGFR mutation-positive NSCLC. The treatment of uncommon EGFR mutation-positive NSCLCs is controversial. Here, we present the case of an 81-year-old man who was diagnosed with lung adenocarcinoma cStage IVA harboring the uncommon EGFR L861Q mutation. The patient received oral afatinib treatment (40 mg/day). One month after the initiation of afatinib treatment, Common Terminology Criteria for Adverse Events version 4.0 grade 2 stomatitis was observed. It improved upon afatinib withdrawal. After 10 days of withdrawal, afatinib treatment was resumed at a reduced dose of 20 mg/day. Subsequently, the patient continued treatment with afatinib. A partial response to afatinib treatment was maintained for 49 months until primary tumor regrowth. Afatinib treatment was continued after disease progression, but the patient died of bacterial pneumonia 59 months after initiation of afatinib treatment. Several studies have previously reported a large number of compound mutations with uncommon mutations, and that compound mutation-induced cells are most susceptible to afatinib. This suggests the efficacy of afatinib in clinical practice and that afatinib may be safely administered to elderly patients with appropriate dose reductions.

摘要

表皮生长因子受体(EGFR)酪氨酸激酶抑制剂是携带 EGFR 突变的非小细胞肺癌(NSCLC)患者的标准治疗方法。罕见突变,除外显子 19 缺失和外显子 21 L858R,占 EGFR 突变阳性 NSCLC 的 7%-23%。罕见 EGFR 突变阳性 NSCLC 的治疗存在争议。在这里,我们报告了一例 81 岁男性患者,被诊断为肺腺癌 cStage IVA,携带罕见的 EGFR L861Q 突变。该患者接受了口服阿法替尼治疗(40mg/天)。阿法替尼治疗开始一个月后,观察到常见不良事件术语标准 4.0 级 2 级口腔炎。停药后有所改善。停药 10 天后,阿法替尼以 20mg/天的剂量恢复治疗。随后,该患者继续接受阿法替尼治疗。阿法替尼治疗的部分缓解持续了 49 个月,直到原发肿瘤复发。疾病进展后继续阿法替尼治疗,但患者在开始阿法替尼治疗 59 个月后死于细菌性肺炎。以前的几项研究报告了大量罕见突变的复合突变,并且复合突变诱导的细胞对阿法替尼最敏感。这表明阿法替尼在临床实践中的疗效,并且可以通过适当的剂量减少安全地为老年患者使用阿法替尼。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06b/7952783/4489864a85f8/TCA-12-989-g002.jpg

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