Dang Michaël, Schritz Anna, Goncharenko Nikolai, Berchem Guy
Department of Oncology, Centre Hospitalier de Luxembourg (CHL), Luxembourg.
University of Luxembourg (Uni.lu), Luxembourg.
Mol Oncol. 2025 May;19(5):1508-1516. doi: 10.1002/1878-0261.13785. Epub 2024 Dec 11.
High-throughput genomic analyses are being implemented in clinical practice. MODIFY is a retrospective study of the first introduction of genomic profiling and molecular tumor boards in the country of Luxembourg. The primary objective was to assess whether patients derived a clinical benefit by measuring the percentage of patients who presented a progression-free survival (PFS) on matched therapy (PFS2) 1.3-fold longer than PFS on previous therapy (PFS1). A total of 94 patients were included. In total, 45 patients (53.57% of patients with successful next-generation sequencing [NGS] analysis) were found to have an actionable mutation. Of these, 11 patients received the treatment recommended by the molecular tumor board, another 12 received best-supportive care, and 20 were treated with conventional therapy. PFS2 and PFS1 data were available for eight patients. The PFS2/PFS1 ratio was ≥ -1.3 in 62.5% (n = 5/8; CI [30.38, 86.51]) of patients; three patients showed a partial response, and median overall survival (OS) was 7.3 months. Although the examined population was small, this study further supports evidence indicating that patients with advanced cancer benefit from molecular profiling and targeted therapy.
高通量基因组分析正在临床实践中得到应用。MODIFY是一项关于卢森堡首次引入基因组分析和分子肿瘤学委员会的回顾性研究。主要目的是通过测量接受匹配治疗的患者无进展生存期(PFS2)比先前治疗的PFS(PFS1)长1.3倍的患者百分比,来评估患者是否获得临床益处。总共纳入了94例患者。总共发现45例患者(成功进行下一代测序[NGS]分析的患者中的53.57%)有可操作的突变。其中,11例患者接受了分子肿瘤学委员会推荐的治疗,另外12例接受了最佳支持治疗,20例接受了传统治疗。8例患者有PFS2和PFS1数据。62.5%(n = 5/8;CI [30.38, 86.51])的患者PFS2/PFS1比值≥ -1.3;3例患者显示部分缓解,中位总生存期(OS)为7.3个月。尽管研究人群规模较小,但这项研究进一步支持了证据,表明晚期癌症患者可从分子分析和靶向治疗中获益。