A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib

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 previo...

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Main Authors: Mehmet Artaç, Levent Korkmaz, Mustafa Karaağaç, Buğra Kaya, Necdet Poyraz, Hakan Özön, Zehra Er, Lema Tavlı
Format: Article
Language:English
Published: Galenos Publishing House 2018-08-01
Series:Journal of Oncological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S2452336417301085
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author Mehmet Artaç
Levent Korkmaz
Mustafa Karaağaç
Buğra Kaya
Necdet Poyraz
Hakan Özön
Zehra Er
Lema Tavlı
author_facet Mehmet Artaç
Levent Korkmaz
Mustafa Karaağaç
Buğra Kaya
Necdet Poyraz
Hakan Özön
Zehra Er
Lema Tavlı
author_sort Mehmet Artaç
collection DOAJ
description 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
format Article
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institution Matheson Library
issn 2452-3364
language English
publishDate 2018-08-01
publisher Galenos Publishing House
record_format Article
series Journal of Oncological Sciences
spelling doaj-art-b51e5cc167bc474092100efa8a5e8bba2025-08-02T17:20:19ZengGalenos Publishing HouseJournal of Oncological Sciences2452-33642018-08-0142111113A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinibMehmet Artaç0Levent Korkmaz1Mustafa Karaağaç2Buğra Kaya3Necdet Poyraz4Hakan Özön5Zehra Er6Lema Tavlı7Necmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, Turkey; Corresponding author. Necmettin Erbakan University, Meram Medical Faculty, Department of Medical Oncology, 42080, Konya, Turkey.Necmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, TurkeyNecmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, TurkeyNecmettin Erbakan University, Meram Faculty of Medicine, Department of Nuclear Medicine, Konya, TurkeyNecmettin Erbakan University, Meram Faculty of Medicine, Department of Radiology, Konya, TurkeyIstanbul Genetics Laboratory, Istanbul, TurkeyNecmettin Erbakan University, Meram Faculty of Medicine, Department of Medical Oncology, Konya, TurkeyNecmettin Erbakan University, Meram Faculty of Medicine, Department of Pathology, Konya, TurkeyConcomitant 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, Crizotinibhttp://www.sciencedirect.com/science/article/pii/S2452336417301085
spellingShingle Mehmet Artaç
Levent Korkmaz
Mustafa Karaağaç
Buğra Kaya
Necdet Poyraz
Hakan Özön
Zehra Er
Lema Tavlı
A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
Journal of Oncological Sciences
title A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
title_full A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
title_fullStr A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
title_full_unstemmed A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
title_short A lung adenocarcinoma patient with EGFR mutation in exon 18 and ALK-rearrangement who treated with erlotinib and crizotinib
title_sort lung adenocarcinoma patient with egfr mutation in exon 18 and alk rearrangement who treated with erlotinib and crizotinib
url http://www.sciencedirect.com/science/article/pii/S2452336417301085
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