分子测序系统对消化道肿瘤诊断的影响:法国中心的经验

B. D. Rauglaudre, E. Norguet-Monnereau, M. Duluc, I. Nanni, J. Mancini, L. Dahan
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摘要

基于肿瘤的分子谱分析在精准医学领域的应用日益广泛。它们的常规使用仍然受到肿瘤材料的可及性、成本和可用性的限制。材料与方法:我们回顾性分析在诊断时接受分子高通量测序(NGS)分析的消化系统癌患者的治疗和生存资料。这项单中心研究的主要目的是比较接受分子匹配治疗的患者与接受标准治疗的患者的总生存率。从最初的疾病诊断到死亡计算中位总生存期。结果:2018年1月至2020年11月期间,528例患者被转介到马赛Timone医院消化肿瘤科治疗消化癌,并接受了高通量分子测序。其中461例患者为消化道癌(其中75例因存在GIST或神经内分泌肿瘤、消化道外癌的消化道定位或未在本中心随访而被排除),275例患者有转移性疾病(同步或异时性)。对于转移性患者,95名患者(43.5%)发现了可操作的分子改变,13名患者(4.7%)接受了分子匹配治疗。接受匹配治疗的患者与未接受分子匹配治疗的患者的中位总生存期无显著差异(2.89 [95%CI 1.84 - 3.93] vs. 2.86 [95%CI 1.52 - 4.19], p=0.671)。结论:本研究提示高通量基因组学可以改善患者的管理。尽管这些结果并没有显示出具有这种可操作的分子改变并接受分子匹配治疗的肿瘤患者的总体生存率比未接受分子匹配治疗的患者高,但它们是有希望的。需要随机试验来证实以NGS为基础的匹配治疗对患者有益处。
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Impact of a Molecular Sequencing Systematic at Diagnosis in Digestive Oncology: Experience of a French Center
Introduction: Tumor-based molecular profiling has increased in the area of precision medicine. Their routine use is still limited by accessibility, cost and availability of tumor material. Materials and Methods: We retrospectively analysed the treatment received and the survival data of patients with digestive cancer who received molecular high-throughput sequencing (NGS) analyses at diagnosis. The primary objective of this single-center study was to compare the overall survival of patients who were treated with molecularly matched therapy with patients who received standard therapy. Median overall survival was calculated from initial disease diagnosis to death. Results: 528 patients were referred to the Digestive Oncology Department of the Timone Hospital in Marseille between January 2018, and November 2020 for management of digestive cancer and received high-throughput molecular sequencing. Among them, 461 patients had a digestive carcinoma (75 of them were excluded because of the presence of a GIST or a neuroendocrine tumor, a digestive localization of extra digestive cancer or the absence of follow-up in our center) and 275 had metastatic disease (synchronous or metachronous). For metastatic patients, actionable molecular alterations were identified in95 patients (43.5%) and for 13 patients (4.7%) a molecularly matched therapy was administered. There was no significant difference in median overall survival between patients who received matched therapy than patients who did not receive molecularly matched therapy (2.89 [95%CI 1.84 - 3.93] vs. 2.86 [95%CI 1.52 - 4.19], p=0.671). Conclusion: This study suggests that high-throughput genomics can improve management of patients. Although these results did not show a benefit in overall survival for tumors who harboured such actionable molecular alterations and who received molecularly matched therapy, than patients who did not receive molecularly matched therapy, they are promising. Randomized trials are needed to confirm that there is a benefit to treating patients with matched therapy based on NGS.
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