Wang Tiantian, Wei Li, Lu Qiang, Shao Yanmei, You Shuqing, Yin Jiani C, Wang Sha, Shao Yang, Chen Zhanhong, Wang Zhe
Department of Medical Oncology and Guangdong Key Laboratory of Liver Disease, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510000, China.
Department of Thoracic Surgery, Tangdu Hospital, The Air Force Military Medical University, Xi'an, 710038, China.
NPJ Precis Oncol. 2022 Nov 11;6(1):84. doi: 10.1038/s41698-022-00325-0.
Recurrent fusions of receptor tyrosine kinases (RTKs) are often driving events in tumorigenesis that carry important diagnostic value and are potentially targetable by the increasing number of tyrosine kinase inhibitors (TKIs). Here, we characterized the spectrum of 1324 RTK fusions with intact kinase domains in solid tumors by DNA-based high-throughput sequencing. Overall, the prevalence of RTK fusions were 4.7%, with variable frequencies and diverse genomic structures and fusion partners across cancer types. Cancer types, such as thyroid cancers, urological cancers and neuroendocrine tumors are selective in the RTK fusions they carry, while others exhibit highly complex spectra of fusion events. Notably, most RTKs were promiscuous in terms of the partner genes they recombine with. A large proportion of RTK fusions had one of the breakpoints localized to intergenic regions. Comprehensive genomic profiling revealed differences in co-mutational patterns pre- and post-TKI treatments across various RTK fusions. At baseline, multiple cases were detected with co-occurring RTK fusions or concomitant oncogenic mutations in driver genes, such as KRAS and EGFR. Following TKI resistance, we observed differences in potential on- and off-target resistance mutations among fusion variants. For example, the EML4-ALK v3 variant displayed more complex on-target resistance mechanisms, which might explain the reduced survival outcome compared with the v1 variant. Finally, we identified two lung cancer patients with MET+ and NTRK1+ tumors, respectively, who responded well to crizotinib treatment. Taken together, our findings demonstrate the diagnostic and prognostic values of screening for RTK fusions using DNA-based sequencing in solid tumors.
受体酪氨酸激酶(RTK)的复发性融合通常是肿瘤发生过程中的驱动事件,具有重要的诊断价值,并且随着酪氨酸激酶抑制剂(TKI)数量的增加,它们有可能成为靶向治疗的对象。在这里,我们通过基于DNA的高通量测序对实体瘤中1324个具有完整激酶结构域的RTK融合进行了特征分析。总体而言,RTK融合的发生率为4.7%,在不同癌症类型中频率各异,基因组结构和融合伴侣也多种多样。甲状腺癌、泌尿系统癌症和神经内分泌肿瘤等癌症类型在其携带的RTK融合方面具有选择性,而其他癌症则表现出高度复杂的融合事件谱。值得注意的是,大多数RTK在与其重组的伴侣基因方面具有混杂性。很大一部分RTK融合的断点之一位于基因间区域。全面的基因组分析揭示了不同RTK融合在TKI治疗前后共突变模式的差异。在基线时,检测到多例同时存在RTK融合或驱动基因(如KRAS和EGFR)中伴随致癌突变的病例。在TKI耐药后,我们观察到融合变体之间潜在的靶向和非靶向耐药突变存在差异。例如,EML4-ALK v3变体表现出更复杂的靶向耐药机制,这可能解释了与v1变体相比生存结果降低的原因。最后,我们分别鉴定出两名患有MET+和NTRK1+肿瘤的肺癌患者,他们对克唑替尼治疗反应良好。综上所述,我们的研究结果证明了在实体瘤中使用基于DNA的测序筛查RTK融合的诊断和预后价值。