With medical progress in cancer therapy, tyrosine kinase inhibitors (TKIs) became a standard of care for many cancer types. But the broad range of possible targeted therapies was accompanied by a plethora of potential resistance mechanisms, of which many have still to be identified. Here, we present the case of a patient with an translocated non-small-cell lung cancer treated with four different TKIs. Her tumor developed not only a well-known -TKI resistance mutation but also underwent a histological transformation from adenocarcinoma to squamous cell carcinoma. To confirm a shared monoclonal origin of the phenotypically different tumors, a phylogenetic reconstruction was conducted: This revealed a cluster of mutations including , , and , which are possible triggering events for the transformation.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059782 | PMC |
http://dx.doi.org/10.1101/mcs.a006156 | DOI Listing |
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