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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 T790M point mutation: a case report
被引:7
|作者:
Nukii, Yuki
[1
]
Miyamoto, Atsushi
[1
,2
]
Mochizuki, Sayaka
[1
]
Moriguchi, Shuhei
[2
]
Takahashi, Yui
[2
]
Ogawa, Kazumasa
[2
]
Murase, Kyoko
[2
]
Hanada, Shigeo
[2
]
Uruga, Hironori
[2
]
Takaya, Hisashi
[2
]
Morokawa, Nasa
[2
]
Kishi, Kazuma
[1
,2
]
机构:
[1] Toranomon Hosp Branch, Dept Resp Med, Takatsu Ku, 1-3-1 Kajigaya, Kawasaki, Kanagawa 2138587, Japan
[2] Toranomon Gen Hosp, Resp Ctr, Dept Resp Med, Minato Ku, 2-2-2 Toranomon, Tokyo 1058470, Japan
来源:
关键词:
Receptor;
epidermal growth factor;
Protein kinase inhibitors;
Lung neoplasms;
Osimertinib;
Pneumatosis intestinalis;
CANCER;
THERAPY;
BENIGN;
TRIAL;
D O I:
10.1186/s12885-019-5399-5
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundPneumatosis 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 presentationA 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 (T790M) 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 12.2months, with an overall duration of administration of 19.4months (581days), osimertinib was continued during beyond-progressive disease status, until a few days before the patient died of lung cancer.ConclusionsPneumatosis 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.
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页数:7
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