Identification of atypical ATRNL1 insertion to EML4-ALK fusion gene in NSCLC
Language English Country Ireland Media print-electronic
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
PubMed
25601488
DOI
10.1016/j.lungcan.2015.01.002
PII: S0169-5002(15)00003-3
Knihovny.cz E-resources
- Keywords
- ATRNL1, Crizotinib, EML4-ALK, Lung cancer, NSCLC, Targeted therapy,
- MeSH
- Oncogene Proteins, Fusion chemistry genetics MeSH
- Protein Kinase Inhibitors therapeutic use MeSH
- Mutagenesis, Insertional * MeSH
- Crizotinib MeSH
- Middle Aged MeSH
- Humans MeSH
- Molecular Sequence Data MeSH
- Lung Neoplasms diagnosis drug therapy genetics MeSH
- Carcinoma, Non-Small-Cell Lung diagnosis drug therapy genetics MeSH
- Pyrazoles therapeutic use MeSH
- Pyridines therapeutic use MeSH
- Radiography, Thoracic MeSH
- Base Sequence MeSH
- Sequence Analysis, DNA MeSH
- Neoplasm Staging MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- EML4-ALK fusion protein, human MeSH Browser
- Oncogene Proteins, Fusion MeSH
- Protein Kinase Inhibitors MeSH
- Crizotinib MeSH
- Pyrazoles MeSH
- Pyridines MeSH
We herein present a rare case of an EML4-ALK positive patient. A 61-year-old man was diagnosed with locoregional non-small cell lung cancer (NSCLC). No EGFR mutations were detected, and therefore the ALK rearrangement was evaluated using immunohistochemistry (IHC), fluorescence in situ hybridization (FISH) and the reverse transcription PCR (RT-PCR) method for EML4-ALK. All methods showed a positive result and, therefore, the patient was treated with crizotinib with a good therapeutic response. However, a detailed RT-PCR analysis and sequencing revealed an unexpected 138 bp insertion of attractin-like 1 (ATRNL1) gene into the EML4-ALK fusion gene. In our case, the positive therapeutic response suggests that ATRNL1 insertion does not affect EML4-ALK's sensitivity to crizotinib. This case shows great EML4-ALK heterogeneity and also that basic detection methods (IHC, FISH) cannot fully specify ALK rearrangement but in many cases a full specification seems to be important for an effective TKI indication, and sequencing ALK variants might contribute to optimized patient selection.
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