Hilton Laura K, Ngu Henry S, Collinge Brett, Dreval Kostiantyn, Ben-Neriah Susana, Rushton Christopher K, Wong Jasper C H, Cruz Manuela, Roth Andrew, Boyle Merrill, Meissner Barbara, Slack Graham W, Farinha Pedro, Craig Jeffrey W, Gerrie Alina S, Freeman Ciara L, Villa Diego, Crump Michael, Shepherd Lois, Hay Annette E, Kuruvilla John, Savage Kerry J, Kridel Robert, Karsan Aly, Marra Marco A, Sehn Laurie H, Steidl Christian, Morin Ryan D, Scott David W
Centre for Lymphoid Cancer, BC Cancer Research Institute, Vancouver, BC, Canada.
Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, Canada.
medRxiv. 2023 Mar 8:2023.03.06.23286584. doi: 10.1101/2023.03.06.23286584.
Diffuse large B-cell lymphoma (DLBCL) is cured in over 60% of patients, but outcomes are poor for patients with relapsed or refractory disease (rrDLBCL). Here, we performed whole genome/exome sequencing (WGS/WES) on tumors from 73 serially-biopsied patients with rrDLBCL. Based on the observation that outcomes to salvage therapy/autologous stem cell transplantation are related to time-to-relapse, we stratified patients into groups according to relapse timing to explore the relationship to genetic divergence and sensitivity to salvage immunochemotherapy. The degree of mutational divergence increased with time between biopsies, yet tumor pairs were mostly concordant for cell-of-origin, oncogene rearrangement status and genetics-based subgroup. In patients with highly divergent tumors, several genes acquired exclusive mutations independently in each tumor, which, along with concordance of genetics-based subgroups, suggests that the earliest mutations in a shared precursor cell constrain tumor evolution. These results suggest that late relapses commonly represent genetically distinct and chemotherapy-naïve disease.
弥漫性大B细胞淋巴瘤(DLBCL)在超过60%的患者中可被治愈,但复发或难治性疾病(rrDLBCL)患者的预后较差。在此,我们对73例接受系列活检的rrDLBCL患者的肿瘤进行了全基因组/外显子组测序(WGS/WES)。基于挽救治疗/自体干细胞移植的疗效与复发时间相关这一观察结果,我们根据复发时间将患者分层,以探讨其与基因差异及挽救性免疫化疗敏感性之间的关系。活检之间的时间间隔越长,突变差异程度越大,但肿瘤对在起源细胞、致癌基因重排状态和基于遗传学的亚组方面大多是一致的。在肿瘤差异很大的患者中,每个肿瘤中有几个基因独立获得了排他性突变,这与基于遗传学的亚组的一致性一起,表明共享前体细胞中的最早突变限制了肿瘤的进化。这些结果表明,晚期复发通常代表基因上不同且未接受过化疗的疾病。