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.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
28 Feb 2019
Historique:
received: 13 12 2018
accepted: 20 02 2019
entrez: 2 3 2019
pubmed: 2 3 2019
medline: 14 6 2019
Statut: epublish

Résumé

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. 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. 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.

Sections du résumé

BACKGROUND 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 METHODS
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 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.

Identifiants

pubmed: 30819142
doi: 10.1186/s12885-019-5399-5
pii: 10.1186/s12885-019-5399-5
pmc: PMC6394003
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Piperazines 0
Protein Kinase Inhibitors 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

186

Références

Arch Surg. 2003 Jan;138(1):68-75
pubmed: 12511155
Gastroenterology. 2005 Apr;128(4):975-86
pubmed: 15825079
AJR Am J Roentgenol. 2007 Jun;188(6):1604-13
pubmed: 17515383
Eur J Med Res. 2009 Jun 18;14(6):231-9
pubmed: 19541582
Nihon Kokyuki Gakkai Zasshi. 2010 Dec;48(12):972-5
pubmed: 21226307
J Thorac Oncol. 2012 Jan;7(1):257
pubmed: 22173663
BMC Cancer. 2012 Mar 10;12:87
pubmed: 22405425
Int J Urol. 2012 Nov;19(11):1041-2
pubmed: 22788573
AJR Am J Roentgenol. 2012 Dec;199(6):1259-65
pubmed: 23169717
AJR Am J Roentgenol. 2013 May;200(5):1042-7
pubmed: 23617487
Ann Surg. 1990 Aug;212(2):160-5
pubmed: 2375647
J Clin Oncol. 2013 Sep 20;31(27):3335-41
pubmed: 23816963
World J Gastroenterol. 2013 Aug 14;19(30):4973-8
pubmed: 23946603
Lung Cancer. 2014 Dec;86(3):339-43
pubmed: 25453619
Oncol Lett. 2015 Sep;10(3):1775-1782
pubmed: 26622749
Lancet. 2016 Apr 2;387(10026):1415-1426
pubmed: 26777916
World J Surg Oncol. 2016 Jun 29;14(1):175
pubmed: 27495256
N Engl J Med. 2017 Feb 16;376(7):629-640
pubmed: 27959700
N Engl J Med. 2018 Jan 11;378(2):113-125
pubmed: 29151359

Auteurs

Yuki Nukii (Y)

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

Atsushi Miyamoto (A)

Department of Respiratory Medicine, Toranomon Hospital (Branch), 1-3-1 Kajigaya Takatsu-ku, Kawasaki-shi, Kanagawa, 213-8587, Japan. atsushimotty@gmail.com.
Department of Respiratory Medicine, Respiratory Center, Toranomon Hospital, 2-2-2 Toranomon Minato-ku, Tokyo, 105-8470, Japan. atsushimotty@gmail.com.

Sayaka Mochizuki (S)

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

Shuhei Moriguchi (S)

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

Yui Takahashi (Y)

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

Kazumasa Ogawa (K)

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

Kyoko Murase (K)

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

Shigeo Hanada (S)

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

Hironori Uruga (H)

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

Hisashi Takaya (H)

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

Nasa Morokawa (N)

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

Kazuma Kishi (K)

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.

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Classifications MeSH