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
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.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Osimertinib in patients with advanced epidermal growth factor receptor T790M mutation-positive non-small cell lung cancer: rationale, evidence and place in therapy
    Ricciuti, Biagio
    Baglivo, Sara
    Paglialunga, Luca
    De Giglio, Andrea
    Bellezza, Guido
    Chiari, Rita
    Crino, Lucio
    Metro, Giulio
    THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2017, 9 (06) : 387 - 403
  • [42] FDA Benefit-Risk Assessment of Osimertinib for the Treatment of Metastatic Non-Small Cell Lung Cancer Harboring Epidermal Growth Factor Receptor T790M Mutation
    Odogwu, Lauretta
    Mathieu, Luckson
    Goldberg, Kirsten B.
    Blumenthal, Gideon M.
    Larkins, Erin
    Fiero, Mallorie H.
    Rodriguez, Lisa
    Bijwaard, Karen
    Lee, Eunice Y.
    Philip, Reena
    Fan, Ingrid
    Donoghue, Martha
    Keegan, Patricia
    McKee, Amy
    Pazdur, Richard
    ONCOLOGIST, 2018, 23 (03): : 353 - 359
  • [43] Successful osimertinib treatment in a patient who exhibited intramedullary spinal cord metastases of lung adenocarcinoma with an acquired EGFR T790M mutation
    Horiuchi, Kohei
    Asakura, Takanori
    Sakaguchi, Shinji
    Saito, Fumitake
    BMJ CASE REPORTS, 2019, 12 (06)
  • [44] Lung adenocarcinoma harboring L858R and T790M mutations in epidermal growth factor receptor, with poor response to gefitinib: A case report
    Wang, Yue Feng
    Xiang, Xianhong
    Pei, Xiaojuan
    Li, Shuhua
    Tang, Cuilan
    Wang, Liantang
    Ke, Zun-Fu
    ONCOLOGY LETTERS, 2014, 8 (03) : 1039 - 1042
  • [45] Complete Response to Afatinib in Lung Adenocarcinoma of Epidermal Growth Factor Receptor Exon-19 Deletion Mutation and Disease Recurrence on Drug Discontinuation
    Kumari, Rashmi
    James, Emmanuel
    Pavithran, K.
    JOURNAL OF PHARMACOLOGY & PHARMACOTHERAPEUTICS, 2018, 9 (04) : 191 - 194
  • [46] Transformation of epidermal growth factor receptor T790M mutation-positive adenosquamous carcinoma of the lung to small cell carcinoma and large-cell neuroendocrine carcinoma following osimertinib therapy: an autopsy case report
    Moriguchi, Shuhei
    Uruga, Hironori
    Fujii, Takeshi
    Yasunaga, Yoichi
    Takahashi, Yui
    Kishi, Kazuma
    RESPIROLOGY CASE REPORTS, 2019, 7 (03):
  • [47] First-line osimertinib treatment in a patient with lung adenocarcinoma with coexisting epidermal growth factor receptor G719S and de novo T790M mutations
    Ito, Noriaki
    Masuda, Takeshi
    Ooka, Ikuko
    Hosoya, Takatsune
    Yamaguchi, Kakuhiro
    Sakamoto, Shinjiro
    Horimasu, Yasushi
    Nakashima, Taku
    Miyamoto, Shintaro
    Iwamoto, Hiroshi
    Fujitaka, Kazunori
    Hamada, Hironobu
    Hattori, Noboru
    THORACIC CANCER, 2022, 13 (05) : 771 - 774
  • [48] Case report: primary resistance to osimertinib in erlotinib-pretreated lung adenocarcinoma with EGFR T790 M mutation
    Lin-Peng Zheng
    Li-Ying Chen
    Xing-Yun Liao
    Zi-Han Xu
    Zheng-Tang Chen
    Jian-Guo Sun
    BMC Cancer, 18
  • [49] The Association of Acquired T790M Mutation with Clinical Characteristics after Resistance to First-Line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor in Lung Adenocarcinoma
    Huang, Yen-Hsiang
    Hsu, Kuo-Hsuan
    Tseng, Jeng-Sen
    Chen, Kun-Chieh
    Hsu, Chia-Hung
    Su, Kang-Yi
    Chen, Jeremy J. W.
    Chen, Huei-Wen
    Yu, Sung-Liang
    Yang, Tsung-Ying
    Chang, Gee-Chen
    CANCER RESEARCH AND TREATMENT, 2018, 50 (04): : 1294 - 1303
  • [50] Oncogenic activity of epidermal growth factor receptor kinase mutant alleles is enhanced by the T790M drug resistance mutation
    Godin-Heymann, Nadia
    Bryant, Ianthe
    Rivera, Miguel N.
    Ulkus, Lindsey
    Bell, Daphne W.
    Riese, David J.
    Settleman, Jeffrey
    Haber, Daniel A.
    CANCER RESEARCH, 2007, 67 (15) : 7319 - 7326