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Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment

BACKGROUND: The clinical significance of majority oncogenic novel fusions is still unknown due to scarcity. Reciprocal ROS1 translocation is a rare form of ROS1 fusion and has not yet been clearly analyzed. CASE PRESENTATION: A 44-year-old Chinese woman with a large dimension in the left lobe of the...

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Autores principales: Zhang, Xugang, Wang, Baoming, Wang, Chunyang, Liao, Chengde, Wang, Shiping, Cao, Ran, Ma, Tonghui, Wang, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659814/
https://www.ncbi.nlm.nih.gov/pubmed/36387218
http://dx.doi.org/10.3389/fonc.2022.1021342
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author Zhang, Xugang
Wang, Baoming
Wang, Chunyang
Liao, Chengde
Wang, Shiping
Cao, Ran
Ma, Tonghui
Wang, Kun
author_facet Zhang, Xugang
Wang, Baoming
Wang, Chunyang
Liao, Chengde
Wang, Shiping
Cao, Ran
Ma, Tonghui
Wang, Kun
author_sort Zhang, Xugang
collection PubMed
description BACKGROUND: The clinical significance of majority oncogenic novel fusions is still unknown due to scarcity. Reciprocal ROS1 translocation is a rare form of ROS1 fusion and has not yet been clearly analyzed. CASE PRESENTATION: A 44-year-old Chinese woman with a large dimension in the left lobe of the lung was admitted to the hospital with IVB lung adenocarcinoma. It was discovered that intron 28 of ROS1 and intron 6 of CD74 produced a unique reciprocal ROS1 rearrangement. In addition, the dual CD74-ROS1 fusions were discovered using the RNA next-generation sequencing (NGS) findings. Although benefiting from crizotinib and lorlatinib sequential treatment, the overall prognosis of the patient was relatively poor, whose progression-free survival was 4 and 5 months for crizotinib treatment and lorlatinib treatment, respectively. CONCLUSION: In summary, a novel ROS1-CD74 fusion identified by DNA NGS was translated into dual CD74-ROS1 transcripts. Furthermore, this patient with non–small cell lung cancer benefited from consecutive tyrosine kinase inhibitor therapy. Our discovery broadened the range of targetable ROS1 fusions and underlined the importance of sequential DNA and RNA sequencing in identifying uncommon but beneficial fusions, which eventually bring benefits to the patients.
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spelling pubmed-96598142022-11-15 Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment Zhang, Xugang Wang, Baoming Wang, Chunyang Liao, Chengde Wang, Shiping Cao, Ran Ma, Tonghui Wang, Kun Front Oncol Oncology BACKGROUND: The clinical significance of majority oncogenic novel fusions is still unknown due to scarcity. Reciprocal ROS1 translocation is a rare form of ROS1 fusion and has not yet been clearly analyzed. CASE PRESENTATION: A 44-year-old Chinese woman with a large dimension in the left lobe of the lung was admitted to the hospital with IVB lung adenocarcinoma. It was discovered that intron 28 of ROS1 and intron 6 of CD74 produced a unique reciprocal ROS1 rearrangement. In addition, the dual CD74-ROS1 fusions were discovered using the RNA next-generation sequencing (NGS) findings. Although benefiting from crizotinib and lorlatinib sequential treatment, the overall prognosis of the patient was relatively poor, whose progression-free survival was 4 and 5 months for crizotinib treatment and lorlatinib treatment, respectively. CONCLUSION: In summary, a novel ROS1-CD74 fusion identified by DNA NGS was translated into dual CD74-ROS1 transcripts. Furthermore, this patient with non–small cell lung cancer benefited from consecutive tyrosine kinase inhibitor therapy. Our discovery broadened the range of targetable ROS1 fusions and underlined the importance of sequential DNA and RNA sequencing in identifying uncommon but beneficial fusions, which eventually bring benefits to the patients. Frontiers Media S.A. 2022-10-31 /pmc/articles/PMC9659814/ /pubmed/36387218 http://dx.doi.org/10.3389/fonc.2022.1021342 Text en Copyright © 2022 Zhang, Wang, Wang, Liao, Wang, Cao, Ma and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zhang, Xugang
Wang, Baoming
Wang, Chunyang
Liao, Chengde
Wang, Shiping
Cao, Ran
Ma, Tonghui
Wang, Kun
Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title_full Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title_fullStr Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title_full_unstemmed Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title_short Case report: A novel reciprocal ROS1-CD74 fusion in a NSCLC patient partially benefited from sequential tyrosine kinase inhibitors treatment
title_sort case report: a novel reciprocal ros1-cd74 fusion in a nsclc patient partially benefited from sequential tyrosine kinase inhibitors treatment
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659814/
https://www.ncbi.nlm.nih.gov/pubmed/36387218
http://dx.doi.org/10.3389/fonc.2022.1021342
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