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A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report

Rearranged during transfection (RET) gene fusions occur in 0.7% to 2% in lung cancer and 1% to 2% in non-small cell lung cancer. Systemic therapies for RET fusion-positive non-small cell lung cancer consist mostly of targeted therapy with RET inhibitors such as selpercatinib and pralsetinib. To date...

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Autores principales: Zhao, Weidi, Sun, Jia’en, Zhu, Huangkai, Zhao, Guofang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662845/
https://www.ncbi.nlm.nih.gov/pubmed/37478265
http://dx.doi.org/10.1097/MD.0000000000034305
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author Zhao, Weidi
Sun, Jia’en
Zhu, Huangkai
Zhao, Guofang
author_facet Zhao, Weidi
Sun, Jia’en
Zhu, Huangkai
Zhao, Guofang
author_sort Zhao, Weidi
collection PubMed
description Rearranged during transfection (RET) gene fusions occur in 0.7% to 2% in lung cancer and 1% to 2% in non-small cell lung cancer. Systemic therapies for RET fusion-positive non-small cell lung cancer consist mostly of targeted therapy with RET inhibitors such as selpercatinib and pralsetinib. To date, approximately 40 fusion partners have been reported. Herein, we report a novel progesterone immunomodulatory binding factor 1 (PIBF1)-RET gene fusion identified from a stage IA lung adenocarcinoma and was further validated by RNA sequencing analysis. PATIENT CONCERNS: A 55-year-old male smoker was found by chest computed tomography to have a solid nodule in the right lower lobe of the lung and enlarged mediastinal lymph nodes. DIAGNOSES: The patient was then diagnosed with stage IA lung adenocarcinoma (T1N0M0). INTERVENTION: The patient then underwent thoracoscopic lobectomy of the right lower lobe and mediastinal lymph node dissection. Molecular testing with a targeted panel of 8 lung cancer-associated driver genes detected a novel PIBF1-RET (P16:R12) fusion, which putatively encodes a gene in which the first 16 exons of PIBF1 was concatenated to RET exon 13 and its downstream sequence, retaining the RET kinase domain. The genomic translocation was further validated by RNA sequencing with a panel of 115 cancer-associated genes, which found no other aberrations. OUTCOMES: The patient was discharged 3 days after surgery. CONCLUSION: We report a novel PIBF1-RET fusion in early-stage lung adenocarcinoma. This finding expands the spectrum of RET fusion partners and warrants further studies in characterizing the oncogenic role of this genomic aberration and response to RET-targeted therapies.
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spelling pubmed-106628452023-07-21 A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report Zhao, Weidi Sun, Jia’en Zhu, Huangkai Zhao, Guofang Medicine (Baltimore) 5700 Rearranged during transfection (RET) gene fusions occur in 0.7% to 2% in lung cancer and 1% to 2% in non-small cell lung cancer. Systemic therapies for RET fusion-positive non-small cell lung cancer consist mostly of targeted therapy with RET inhibitors such as selpercatinib and pralsetinib. To date, approximately 40 fusion partners have been reported. Herein, we report a novel progesterone immunomodulatory binding factor 1 (PIBF1)-RET gene fusion identified from a stage IA lung adenocarcinoma and was further validated by RNA sequencing analysis. PATIENT CONCERNS: A 55-year-old male smoker was found by chest computed tomography to have a solid nodule in the right lower lobe of the lung and enlarged mediastinal lymph nodes. DIAGNOSES: The patient was then diagnosed with stage IA lung adenocarcinoma (T1N0M0). INTERVENTION: The patient then underwent thoracoscopic lobectomy of the right lower lobe and mediastinal lymph node dissection. Molecular testing with a targeted panel of 8 lung cancer-associated driver genes detected a novel PIBF1-RET (P16:R12) fusion, which putatively encodes a gene in which the first 16 exons of PIBF1 was concatenated to RET exon 13 and its downstream sequence, retaining the RET kinase domain. The genomic translocation was further validated by RNA sequencing with a panel of 115 cancer-associated genes, which found no other aberrations. OUTCOMES: The patient was discharged 3 days after surgery. CONCLUSION: We report a novel PIBF1-RET fusion in early-stage lung adenocarcinoma. This finding expands the spectrum of RET fusion partners and warrants further studies in characterizing the oncogenic role of this genomic aberration and response to RET-targeted therapies. Lippincott Williams & Wilkins 2023-07-21 /pmc/articles/PMC10662845/ /pubmed/37478265 http://dx.doi.org/10.1097/MD.0000000000034305 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5700
Zhao, Weidi
Sun, Jia’en
Zhu, Huangkai
Zhao, Guofang
A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title_full A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title_fullStr A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title_full_unstemmed A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title_short A novel PIBF1-RET gene fusion identified from a stage IA lung adenocarcinoma: A case report
title_sort novel pibf1-ret gene fusion identified from a stage ia lung adenocarcinoma: a case report
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662845/
https://www.ncbi.nlm.nih.gov/pubmed/37478265
http://dx.doi.org/10.1097/MD.0000000000034305
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