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奥希替尼致肺腺癌患者出现肠气肿:一例同时检测到外显子 19 缺失和 T790M 点突变的表皮生长因子受体基因突变患者的病例报告

Pneumatosis intestinalis induced by osimertinib in a patient with lung adenocarcinoma harbouring epidermal growth factor receptor gene mutation with simultaneously detected exon 19 deletion and T790 M point mutation: a case report.

机构信息

Department of Respiratory Medicine, Toranomon Hospital (Branch), 1-3-1 Kajigaya Takatsu-ku, Kawasaki-shi, Kanagawa, 213-8587, Japan.

Department of Respiratory Medicine, Respiratory Center, Toranomon Hospital, 2-2-2 Toranomon Minato-ku, Tokyo, 105-8470, Japan.

出版信息

BMC Cancer. 2019 Feb 28;19(1):186. doi: 10.1186/s12885-019-5399-5.

Abstract

BACKGROUND

Pneumatosis intestinalis is a rare adverse event that occurs in patients with lung cancer, especially those undergoing treatment with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI). Osimertinib is the most recently approved EGFR-TKI, and its usage is increasing in clinical practice for lung cancer patients who have mutations in the EGFR gene.

CASE PRESENTATION

A 74-year-old woman with clinical stage IV (T2aN2M1b) lung adenocarcinoma was determined to have EGFR gene mutations, namely a deletion in exon 19 and a point mutation (T790 M) in exon 20. Osimertinib was started as seventh-line therapy. Follow-up computed tomography on the 97th day after osimertinib administration incidentally demonstrated intra-mural air in the transverse colon, as well as intrahepatic portal vein gas. Pneumatosis intestinalis and portal vein gas improved by fasting and temporary interruption of osimertinib. Osimertinib was then restarted and continued without recurrence of pneumatosis intestinalis. Overall, following progression-free survival of 12.2 months, with an overall duration of administration of 19.4 months (581 days), osimertinib was continued during beyond-progressive disease status, until a few days before the patient died of lung cancer.

CONCLUSIONS

Pneumatosis intestinalis should be noted as an important adverse event that can occur with administration of osimertinib; thus far, such an event has never been reported. This was a valuable case in which osimertinib was successfully restarted after complete recovery from pneumatosis intestinalis, such that further extended administration of osimertinib was achieved.

摘要

背景

肠气肿是一种罕见的不良事件,发生在肺癌患者中,特别是那些正在接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗的患者。奥希替尼是最近批准的 EGFR-TKI,在临床实践中,其在具有 EGFR 基因突变的肺癌患者中的使用正在增加。

病例介绍

一名 74 岁女性,临床分期为 IV 期(T2aN2M1b)肺腺癌,确定存在 EGFR 基因突变,即外显子 19 缺失和外显子 20 点突变(T790M)。奥希替尼开始作为第七线治疗。奥希替尼给药后第 97 天的随访计算机断层扫描偶然发现横结肠壁内空气以及肝内门静脉气体。肠气肿和门静脉气肿通过禁食和暂时中断奥希替尼治疗得到改善。然后重新开始奥希替尼治疗,且未再出现肠气肿。总体而言,无进展生存时间为 12.2 个月,奥希替尼总给药时间为 19.4 个月(581 天),在疾病进展后状态下继续使用奥希替尼,直到患者死于肺癌前几天。

结论

肠气肿应被视为奥希替尼给药时可能发生的重要不良事件;迄今为止,尚未有此类事件的报道。这是一个有价值的病例,奥希替尼在肠气肿完全恢复后成功重新开始使用,从而进一步延长了奥希替尼的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fded/6394003/a7ac99f58d1c/12885_2019_5399_Fig1_HTML.jpg

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