A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALKrearrangement who treated with erlotinib and crizotinib
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Case report
VOLUME: 4 ISSUE: 2
P: 111 - 113
2018

A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALKrearrangement who treated with erlotinib and crizotinib

J Oncol Sci 2018;4(2):111-113
1. Necmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, Turkey
2. Necmettin Erbakan University, Meram Faculty of Medicine, Department of Nuclear Medicine, Konya, Turkey
3. Necmettin Erbakan University, Meram Faculty of Medicine, Department of Radiology, Konya, Turkey
4. Istanbul Genetics Laboratory, Istanbul, Turkey
5. Necmettin Erbakan University, Meram Faculty of Medicine, Department of Pathology, Konya, Turkey
No information available.
No information available
Received Date: 2017-10-20
Accepted Date: 2018-04-24
Online Date: 0000-00-00
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Abstract

Concomitant mutations of echinoderm microtubule-associated protein-like 4 (EML4) anaplastic lymphoma kinase (ALK) translocation and epidermal growth factor receptor (EGFR) can be found rarely in lung adenocarcinoma. We present a case of harboring EML4/ALK rearrangement lung adenocarcinoma who previously received erlotinib. A 42-year-old male who was diagnosed as lung adenocarcinoma and received many series of cytotoxic regimens. A partial tumor response was achieved with crizotinib after failure with erlotinib therapy. After progressive disease, biopsy of new liver lesion showed EML4/ALK rearrangement. Thus crizotinib was administrated. A partial tumor response was achieved with crizotinib after failure with erlotinib therapy and chemotherapy. We conclude that it is important to evaluate for EML4/ALK rearrangement even the patient has EGFR mutation. Concomitant EGFR exon 18 and EML4- ALK mutations can occur in lung adenocarcinoma. EML4/ALK related TKIs may be more effective in these patients.

Keywords:
Non-small cell lung cancer, Erlotinib, Epidermal growth factor receptor, Anaplastic lymphoma kinase, Crizotinib