医学
一致性
肿瘤科
弥漫性大B细胞淋巴瘤
队列
癌症的体细胞进化
外显子组测序
内科学
自体干细胞移植
外显子组
人口
淋巴瘤
活检
癌症
突变
生物
基因
环境卫生
生物化学
作者
Laura K. Hilton,Henry S. Ngu,Brett Collinge,Kostiantyn Dreval,Susana Ben‐Neriah,Christopher Rushton,Jasper Wong,Manuela Cruz,Andrew Roth,Merrill Boyle,Barbara Meissner,Graham W. Slack,Pedro Farinha,Jeffrey W. Craig,Alina S. Gerrie,Ciara L. Freeman,Diego Villa,Judith Anula Rodrigo,Kevin Song,Michael Crump
摘要
Diffuse large B-cell lymphoma (DLBCL) is cured in more than 60% of patients, but outcomes remain poor for patients experiencing disease progression or relapse (refractory or relapsed DLBCL [rrDLBCL]), particularly if these events occur early. Although previous studies examining cohorts of rrDLBCL have identified features that are enriched at relapse, few have directly compared serial biopsies to uncover biological and evolutionary dynamics driving rrDLBCL. Here, we sought to confirm the relationship between relapse timing and outcomes after second-line (immuno)chemotherapy and determine the evolutionary dynamics that underpin that relationship.
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