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胸腺瘤与复发性胸腺瘤的综合基因组分析比较揭示了潜在的靶向治疗药物作用靶点突变。

Comparative Analysis of Comprehensive Genomic Profile in Thymomas and Recurrent Thymomas Reveals Potentially Actionable Mutations for Target Therapies.

机构信息

Thoracic Surgery, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.

Thoracic Surgery, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.

出版信息

Int J Mol Sci. 2024 Sep 3;25(17):9560. doi: 10.3390/ijms25179560.

Abstract

Molecular profiles of thymomas and recurrent thymomas are far from being defined. Herein, we report an analysis of a comprehensive genetic profile (CGP) in a highly selected cohort of recurrent thymomas. Among a cohort of 426 thymomas, the tissue was available in 23 recurrent tumors for matching the biomolecular results obtained from primary and relapse samples. A control group composed of non-recurrent thymoma patients was selected through a propensity score match analysis. CGP was performed using the NGS Tru-SightOncology assay to evaluate TMB, MSI, and molecular alterations in 523 genes. CGP does not differ when comparing initial tumor with tumor relapse. A significantly higher frequency of cell cycle control genes alterations (100.0% vs. 57.1%, = 0.022) is detected in patients with early recurrence (<32 months) compared to late recurrent cases. The CGPs were similar in recurrent thymomas and non-recurrent thymomas. Finally, based on NGS results, an off-label treatment or clinical trial could be potentially proposed in >50% of cases (oncogenic Tier-IIC variants). In conclusion, CGPs do not substantially differ between initial tumor vs. tumor recurrence and recurrent thymomas vs. non-recurrent thymomas. Cell cycle control gene alterations are associated with an early recurrence after thymectomy. Multiple target therapies are potentially available by performing a comprehensive CGP, suggesting that a precision medicine approach on these patients could be further explored.

摘要

胸腺瘤和复发性胸腺瘤的分子谱远未得到明确。在此,我们报告了对一组高度选择的复发性胸腺瘤进行综合遗传分析(CGP)的结果。在 426 例胸腺瘤队列中,23 例复发性肿瘤的组织可用于匹配原发性和复发性样本的生物分子结果。通过倾向评分匹配分析选择了一组非复发性胸腺瘤患者作为对照组。使用 NGS Tru-SightOncology 检测方法进行 CGP,以评估 TMB、MSI 和 523 个基因中的分子改变。比较初始肿瘤与肿瘤复发时,CGP 没有差异。与晚期复发病例相比,早期复发(<32 个月)患者的细胞周期控制基因改变的频率显著更高(100.0%比 57.1%,=0.022)。复发性胸腺瘤和非复发性胸腺瘤的 CGPs 相似。最后,根据 NGS 结果,超过 50%的病例(致癌 Tier-IIC 变体)可能会提出非标签治疗或临床试验。总之,CGP 在初始肿瘤与肿瘤复发以及复发性胸腺瘤与非复发性胸腺瘤之间没有显著差异。细胞周期控制基因改变与胸腺瘤切除术后的早期复发有关。通过进行全面的 CGP,可以提供多种靶向治疗,这表明可以进一步探索这些患者的精准医学方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5167/11394945/65393a88969b/ijms-25-09560-g001.jpg

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