Walker Janek S, Wenzl Kerstin, Novak Joseph P, Stokes Matthew E, Hopper Melissa A, Dropik Abigail R, Siminski Miranda S, Bock Allison M, Sarangi Vivekananda, Ortiz Maria, Stong Nicholas, Huang C Chris, Maurer Matthew J, Link Brian K, Ansell Stephen M, Habermann Thomas M, Witzig Thomas E, King Rebecca L, Nowakowski Grzegorz, Cerhan James R, Gandhi Anita K, Novak Anne J
Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Informatics and Predictive Sciences, Bristol Myers Squibb, Summit, NJ, USA.
Blood Cancer J. 2025 Jul 12;15(1):120. doi: 10.1038/s41408-025-01326-5.
Up to 40% of diffuse large B-cell lymphoma (DLBCL) patients do not experience a durable response to frontline immunochemotherapy, and prospective identification of high-risk cases that may benefit from personalized therapeutic management remains an unmet need. Molecular phenotyping techniques have established a landscape of genomic variants in diagnostic DLBCL; however, these have not yet been applied in large-scale studies of relapsed/refractory DLBCL, resulting in incomplete characterization of mechanisms driving tumor progression and treatment resistance. Here, we performed an integrated multiomic analysis on 228 relapsed/refractory DLBCL samples, including 24 with serial biopsies. Refined cell-of-origin subtyping identified patients harboring GCB and DZsig+ relapsed/refractory tumors in cases with primary refractory disease with remarkably poor outcomes, and comparative analysis of genomic features between relapsed and diagnostic samples identified subtype-specific mechanisms of therapeutic resistance driven by frequent alteration to MYC, BCL2, BCL6, and TP53 among additional strong lymphoma driver genes. Tumor evolution dynamics suggest innate mechanisms of chemoresistance are present in many DLBCL tumors at diagnosis, and that relapsed/refractory tumors are primarily comprised of a homogenous clonal expansion with reduced tumor microenvironment activity. Adaptation of personalized therapeutic strategies targeting DLBCL subtype-specific resistance mechanisms should be considered to benefit these high-risk populations.
高达40%的弥漫性大B细胞淋巴瘤(DLBCL)患者对一线免疫化疗没有持久反应,前瞻性识别可能从个性化治疗管理中获益的高危病例仍然是一个未满足的需求。分子表型分析技术已确定了诊断性DLBCL中的基因组变异情况;然而,这些技术尚未应用于复发/难治性DLBCL的大规模研究,导致驱动肿瘤进展和治疗耐药的机制特征不完整。在此,我们对228例复发/难治性DLBCL样本进行了综合多组学分析,其中包括24例有系列活检的样本。精细的起源细胞亚型分类确定了在原发性难治性疾病病例中携带生发中心B细胞(GCB)和双打击信号阳性(DZsig+)复发/难治性肿瘤的患者,其预后非常差,并且对复发样本和诊断样本的基因组特征进行比较分析,确定了由MYC、BCL2、BCL6和TP53等其他强淋巴瘤驱动基因频繁改变所驱动的亚型特异性治疗耐药机制。肿瘤进化动力学表明,许多DLBCL肿瘤在诊断时就存在化疗耐药的内在机制,并且复发/难治性肿瘤主要由肿瘤微环境活性降低的同质克隆扩增组成。应考虑采用针对DLBCL亚型特异性耐药机制的个性化治疗策略,以使这些高危人群受益。