CASE REPORT
A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALKrearrangement who treated with erlotinib and crizotinib
Received Date : 20 Oct 2017
Accepted Date : 24 Apr 2018
Mehmet Artaç a,*, Levent Korkmaz a, Mustafa Karaağaç a, Buğra Kaya b, Necdet Poyraz c, Hakan Özön d, Zehra Er a, Lema Tavlı e
a Necmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, Turkey
b Necmettin Erbakan University, Meram Faculty of Medicine, Department of Nuclear Medicine, Konya, Turkey
c Necmettin Erbakan University, Meram Faculty of Medicine, Department of Radiology, Konya, Turkey
d Istanbul Genetics Laboratory, Istanbul, Turkey
e Necmettin Erbakan University, Meram Faculty of Medicine, Department of Pathology, Konya, Turkey
Doi: 10.1016/j.jons.2018.04.001 - Article's Language: EN
Journal of Oncological Sciences 4 (2018) 111-113
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