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基于下一代测序的中国多癌回顾性分析中 RET 融合的鉴定。

Identification of RET fusions in a Chinese multicancer retrospective analysis by next-generation sequencing.

机构信息

Department of Thoracic and Cardiovascular Surgery, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.

Department of Translational Medicine, Genetron Health (Beijing) Technology, Co. Ltd., Beijing, China.

出版信息

Cancer Sci. 2022 Jan;113(1):308-318. doi: 10.1111/cas.15181. Epub 2021 Nov 15.

DOI:10.1111/cas.15181
PMID:34710947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8748217/
Abstract

Fusion of RET with different partner genes has been detected in papillary thyroid, lung, colorectal, pancreatic, and breast cancer. Approval of selpercatinib for treatment of lung and thyroid cancer with RET gene mutations or fusions calls for studies to explore RET fusion partners and their eligibility for RET-based targeted therapy. In this study, RET fusion patterns in a large group of Chinese cancer patients covering several cancer types were identified using next-generation sequencing. A total of 44 fusion patterns were identified in the study cohort with KIF5B, CCDC6, and ERC1 being the most common RET fusion partners. Notably, 17 novel fusions were first reported in this study. Prevalence of functional RET fusions was 1.05% in lung cancer, 6.03% in thyroid cancer, 0.39% in colorectal cancer, and less than 0.1% in gastric cancer and hepatocellular carcinoma. Analysis showed a preference for fusion partners in different tumor types, with KIF5B being the common type in lung cancer, CCDC6 in thyroid cancer, and NCOA4 in colorectal cancer. Co-occurrence of EGFR mutations and RET fusions with rare partner genes (rather than KIF5B) in lung cancer patients was correlated with epidermal growth factor receptor-tyrosine kinase inhibitor resistance and could predict response to targeted therapies. Findings from this study provide a guide to clinicians in determining tumors with specific fusion patterns as candidates for RET targeted therapies.

摘要

RET 与不同伙伴基因的融合已在甲状腺乳头状癌、肺癌、结直肠癌、胰腺癌和乳腺癌中被检测到。塞尔帕替尼(一种 RET 基因突变为基础的靶向药物)获批用于治疗具有 RET 基因突变或融合的肺癌和甲状腺癌,这需要研究来探索 RET 融合伙伴及其是否适合基于 RET 的靶向治疗。在这项研究中,使用下一代测序技术在涵盖多种癌症类型的中国癌症患者的大样本中确定了 RET 融合模式。在研究队列中确定了 44 种融合模式,其中 KIF5B、CCDC6 和 ERC1 是最常见的 RET 融合伙伴。值得注意的是,本研究首次报道了 17 种新的融合。功能性 RET 融合在肺癌中的患病率为 1.05%,甲状腺癌为 6.03%,结直肠癌为 0.39%,胃癌和肝细胞癌则低于 0.1%。分析显示不同肿瘤类型对融合伙伴有偏好,KIF5B 是肺癌的常见类型,CCDC6 是甲状腺癌的常见类型,NCOA4 是结直肠癌的常见类型。在肺癌患者中,EGFR 突变和 RET 融合与罕见伙伴基因(而非 KIF5B)共同存在与表皮生长因子受体酪氨酸激酶抑制剂耐药有关,并可预测对靶向治疗的反应。本研究的结果为临床医生确定具有特定融合模式的肿瘤作为 RET 靶向治疗的候选者提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/4debe0740b3f/CAS-113-308-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/4debe0740b3f/CAS-113-308-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/c8b14642529d/CAS-113-308-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/caba3e4d46fa/CAS-113-308-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/75215d01a4b5/CAS-113-308-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/bd7f09d7732c/CAS-113-308-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/54b10c1c1048/CAS-113-308-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b0/8748217/4debe0740b3f/CAS-113-308-g003.jpg

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