Tsilimigras Diamantis I, Stecko Hunter, Moris Dimitrios, Pawlik Timothy M
Department of Surgery, Division of Surgical Oncology, The Ohio State University Wexner Medical Center and James Comprehensive Cancer Center, Columbus, Ohio, USA.
Department of Surgery, Duke University Hospital, Duke University, Durham, North Carolina, USA.
J Surg Oncol. 2025 Jan 13. doi: 10.1002/jso.28081.
Biliary tract cancers (BTCs) represent distinct biological and genomic entities. Anatomic and geographic heterogeneity in genomic profiling of BTC subtypes, genomic co-alterations, and their impact on long-term outcomes are not well defined.
Genomic data to characterize alterations among patients with BTCs were derived from the AACR GENIE registry (v15.1) and other genomic data sets. Patterns of mutational co-occurrence, frequency of co-alterations, and their impact on long-term outcomes among BTC patients were examined.
Alterations in IDH1 and FGFR2 genes were mostly noted among intrahepatic cholangiocarcinoma (iCCA) samples, TP53, ERBB2/HER2, and SMAD4 mutations were more frequent among gallbladder cancer (GBC) samples while extrahepatic cholangiocarcinoma (eCCA) more commonly harbored KRAS mutations (all Q < 0.001). Alterations in IDH1 and FGFR2 genes were more frequent among iCCA samples from Western vs. Eastern populations, while KRAS, SMAD4, and ERBB2 mutations were more commonly observed among Eastern populations(all Q < 0.05). FGFR2 gene was frequently co-mutated with BAP1 (log2OR: 1.55, Q < 0.001), while IDH1 gene was commonly co-mutated with PBRM1 (log2OR: 1.09, Q < 0.001). Co-alteration rate among patients with IDH1-mutant iCCAs, FGFR2-rearranged iCCAs, KRAS-mutant eCCA, and HER2-mutant GBCs were 80.8%, 85.2%, 76.7%, and 100%, respectively. Among patients with iCCA and FGFR2 fusions/rearrangements, harboring co-alterations in the TP53 pathway or PI3K pathway correlated with worse overall survival (OS), while patients with IDH1-mutant iCCA had worse OS when harboring co-alterations in the cell cycle pathway.
Marked genomic heterogeneity exists among patients with BTCs based on anatomic and geographic location. The overwhelming majority of BTC patients with clinically significant mutations had concurrent genomic co-alterations. The current study highlights the molecular complexity of BTCs with multiple alterations that commonly co-exist and could potentially be targeted to treat BTCs.
胆管癌(BTCs)代表不同的生物学和基因组实体。BTC亚型的基因组图谱、基因组共改变及其对长期预后的影响在解剖学和地理上的异质性尚未明确界定。
用于表征BTC患者改变的基因组数据来自美国癌症研究协会(AACR)GENIE注册库(v15.1)和其他基因组数据集。研究了BTC患者中突变共发生模式、共改变频率及其对长期预后的影响。
IDH1和FGFR2基因改变主要见于肝内胆管癌(iCCA)样本,TP53、ERBB2/HER2和SMAD4突变在胆囊癌(GBC)样本中更常见,而肝外胆管癌(eCCA)更常发生KRAS突变(所有Q<0.001)。IDH1和FGFR2基因改变在西方人群的iCCA样本中比东方人群更常见,而KRAS、SMAD4和ERBB2突变在东方人群中更常见(所有Q<0.05)。FGFR2基因常与BAP1共同突变(log2OR:1.55,Q<0.001),而IDH1基因常与PBRM1共同突变(log2OR:1.09,Q<0.001)。IDH1突变型iCCA、FGFR2重排型iCCA、KRAS突变型eCCA和HER2突变型GBC患者的共改变率分别为80.8%、85.2%、76.7%和100%。在iCCA和FGFR2融合/重排患者中,TP53途径或PI3K途径存在共改变与总生存期(OS)较差相关,而IDH1突变型iCCA患者在细胞周期途径存在共改变时OS较差。
基于解剖学和地理位置,BTC患者存在明显的基因组异质性。绝大多数具有临床显著突变的BTC患者同时存在基因组共改变。本研究强调了BTCs分子复杂性,其具有多种常共存的改变,可能成为治疗BTCs的潜在靶点。