| Literature DB >> 27565911 |
Alison C Johnson1, Pascal Dô2, Nicolas Richard3, Catherine Dubos2, Jean Jacques Michels4, Jessica Bonneau5, Radj Gervais2.
Abstract
Anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC) is sensitive to ALK inhibitor therapy, but resistance invariably develops and can be mediated by certain secondary mutations. The detection of these mutations is useful to guide treatment decisions, but tumors are not always easily accessible to re-biopsy. We report the case of a patient with ALK-rearranged NSCLC who presented acquired resistance to crizotinib and then alectinib. Sequencing analyses of DNA from a liver metastasis biopsy sample and circulating tumor DNA both found the same I1171N ALK kinase domain mutation, known to confer resistance to certain ALK inhibitors. However, the patient then received ceritinib, a 2nd generation ALK inhibitor, and achieved another partial response. This case underlines how ALK resistance mutation detection in peripheral blood could be a reliable, safer, and less invasive alternative to tissue-based samples in NSCLC.Entities:
Keywords: ALK; Circulating tumor DNA; Crizotinib; Non-small cell lung cancer; Resistance mutation
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Year: 2016 PMID: 27565911 DOI: 10.1016/j.lungcan.2016.06.010
Source DB: PubMed Journal: Lung Cancer ISSN: 0169-5002 Impact factor: 5.705