A case of lung adenocarcinoma with a novel CD74-ROS1 fusion variant identified by comprehensive genomic profiling that responded to crizotinib and entrectinib.
Mizuha Haraguchi HashiguchiTakashi SatoRinako WatanabeJunko KagyoTomohiko MatsuzakiHideharu DomotoTerufumi KatoYoshiro NakaharaTomoyuki YokoseYukihiko HiroshimaTetsuya ShiomiPublished in: Thoracic cancer (2021)
ROS1 rearrangements are found in 1-2% of patients with non-small-cell lung cancer. The detection of the rearrangements is crucial since clinically effective molecular targeted drugs are available for them. We present a case of lung adenocarcinoma with a previously unknown ROS1-CD74 fusion variant, CD74 exon 3 fused to ROS1 exon 34, which was not detected by a conventional RT-PCR-based test for ROS1 fusion gene detection but identified by hybrid capture-based next-generation sequencing. This tumor responded to crizotinib initially and to entrectinib after relapse with brain metastasis, indicating the oncogenic activity of this novel fusion variant.
Keyphrases
- cell death
- dna damage
- reactive oxygen species
- copy number
- advanced non small cell lung cancer
- genome wide
- white matter
- resting state
- label free
- oxidative stress
- dna methylation
- brain injury
- single cell
- functional connectivity
- quantum dots
- subarachnoid hemorrhage
- sensitive detection
- cell free
- drug induced
- circulating tumor