Vasseur Damien, Abbou Samuel, Lacroix Ludovic, Lamant Laurence, Pata-Merci Noémie, Sibon David, Facchinetti Francesco, Deloger Marc, Braye Floriane, Minard-Colin Véronique, Brugières Laurence, Rouleau Etienne, Friboulet Luc, Rigaud Charlotte
Medical Biology and Pathology Department, Villejuif, France.
AMMICa UAR3655/US23, Villejuif, France.
NPJ Precis Oncol. 2025 May 27;9(1):157. doi: 10.1038/s41698-025-00944-3.
In this multicenter study, we were able to detect circulating tumor DNA (ctDNA) in 87.5% of patients with the rare disease ALK + ALCL. Moreover, by analyzing ctDNA from samples collected at disease progression, we were able to identify resistance mutations to ALK inhibitors. Furthermore, ctDNA proved to be a valuable and consistent tool for monitoring minimal residual disease.
在这项多中心研究中,我们能够在87.5%的罕见病ALK+间变性大细胞淋巴瘤(ALCL)患者中检测到循环肿瘤DNA(ctDNA)。此外,通过分析疾病进展时采集样本中的ctDNA,我们能够识别出对ALK抑制剂的耐药突变。此外,ctDNA被证明是监测微小残留病的一种有价值且可靠的工具。