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Case Report: A Novel Intergenic MIR4299/MIR8070-RET Fusion with RET Amplification and Clinical Response to Pralsetinib in a Lung Adenocarcinoma Patient

Overview
Journal Front Oncol
Specialty Oncology
Date 2022 Oct 13
PMID 36226049
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Abstract

The identification of receptor-tyrosine kinase gene (RET) fusions in lung cancer has become crucial owing to actionable events that predict responsiveness to tyrosine kinase inhibitors (TKIs). However, RET fusions with distinct partner genes respond differently to TKIs. In this case, a 60-year-old man was diagnosed with advanced lung adenocarcinoma. A novel RET-MIR4299/MIR8070 fusion and RET amplification were identified using next-generation sequencing (NGS). The patient was then administered with pralsetinib. After 3 weeks of therapy, the patient had a partial response. At the time of reporting, the patient was on continuous pralsetinib. These findings broaden the range of RET fusion types and provide the basis for the hypothesis that RET intergenic fusion and amplification respond to pralsetinib treatment in lung adenocarcinoma.

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References
1.
Lee J, Hazar-Rethinam M, Decker B, Gjoerup O, Madison R, Lieber D . The Pan-Tumor Landscape of Targetable Kinase Fusions in Circulating Tumor DNA. Clin Cancer Res. 2021; 28(4):728-737. PMC: 9377769. DOI: 10.1158/1078-0432.CCR-21-2136. View

2.
Montrone M, Longo V, Catino A, Pizzutilo P, Galetta D . [Efficacy of pralsetinib in a patient with advanced lung adenocarcinoma positive for RET rearrangement: the importance of Comprehensive Genomic Profiling.]. Recenti Prog Med. 2021; 112(1):10e-13e. DOI: 10.1701/3525.35132. View

3.
Paratala B, Chung J, Williams C, Yilmazel B, Petrosky W, Williams K . RET rearrangements are actionable alterations in breast cancer. Nat Commun. 2018; 9(1):4821. PMC: 6240119. DOI: 10.1038/s41467-018-07341-4. View

4.
Lin J, Liu S, McCoach C, Zhu V, Tan A, Yoda S . Mechanisms of resistance to selective RET tyrosine kinase inhibitors in RET fusion-positive non-small-cell lung cancer. Ann Oncol. 2020; 31(12):1725-1733. PMC: 9538591. DOI: 10.1016/j.annonc.2020.09.015. View

5.
Platt A, Morten J, Ji Q, Elvin P, Womack C, Su X . A retrospective analysis of RET translocation, gene copy number gain and expression in NSCLC patients treated with vandetanib in four randomized Phase III studies. BMC Cancer. 2015; 15:171. PMC: 4412099. DOI: 10.1186/s12885-015-1146-8. View