Division of Hematology, Medical Oncology and Palliative Care, University of Wisconsin, Carbone Cancer Center, Madison, WI.
Division of Hematology and Oncology, Weill Cornell Medicine, New York, NY.
Blood Adv. 2024 Oct 22;8(20):5290-5296. doi: 10.1182/bloodadvances.2024013863.
T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) is a rare histologic variant of LBCL. Limited data regarding CD19-directed chimeric antigen receptor T-cell (CART) therapy in relapsed/refractory (R/R) THRLBCL suggest poor efficacy. We investigated CART outcomes for R/R THRLBCL through the Center for International Blood and Marrow Transplant Research registry. A total of 58 adult patients with R/R THRLBCL who received commercial CD19-CART therapy between 2018 and 2022 were identified. Most patients (67%) had early relapse of disease (45% primary refractory) with a median of 3 (range, 1-7) prior therapies and were treated with axicabtagene ciloleucel (69%). At median follow-up of 23 months after CART therapy, 2-year overall and progression-free survival were 42% (95% confidence interval [CI], 27-57) and 29% (95% CI, 17-43), respectively. In univariable analysis, poor performance status before CART therapy was associated with higher mortality (hazard ratio, 2.35; 95%CI, 1.02-5.5). The 2-year cumulative incidences of relapse/progression and nonrelapse mortality were 69% and 2%, respectively. Grade ≥3 cytokine release syndrome and immune effector cell-associated neurologic syndrome occurred in 7% and 15% of patients, respectively. In this largest analysis of CD19-CART therapy for R/R THRLBCL, ∼30% of patients were alive and progression free 2 years after CART therapy. Despite a high incidence of progression (69% at 2 years), these results suggest a subset of patients with R/R THRLBCL may have durable responses with CARTs.
T 细胞/组织细胞丰富的大 B 细胞淋巴瘤(THRLBCL)是一种罕见的大 B 细胞淋巴瘤组织学亚型。关于复发/难治性(R/R)THRLBCL 中 CD19 导向嵌合抗原受体 T 细胞(CART)治疗的数据有限,表明疗效不佳。我们通过国际血液和骨髓移植研究中心登记处调查了 R/R THRLBCL 的 CART 治疗结果。共确定了 58 例接受商业 CD19-CART 治疗的 R/R THRLBCL 成年患者,这些患者于 2018 年至 2022 年接受治疗。大多数患者(67%)疾病早期复发(45%为原发性难治性),中位治疗前治疗次数为 3(范围 1-7),接受 axicabtagene ciloleucel 治疗(69%)。在接受 CART 治疗后中位随访 23 个月时,2 年总生存率和无进展生存率分别为 42%(95%CI,27-57)和 29%(95%CI,17-43)。在单变量分析中,CART 治疗前的体能状态差与死亡率较高相关(危险比,2.35;95%CI,1.02-5.5)。复发/进展的 2 年累积发生率和非复发死亡率分别为 69%和 2%。分别有 7%和 15%的患者发生了≥3 级细胞因子释放综合征和免疫效应细胞相关神经毒性综合征。在这项最大的 R/R THRLBCL CD19-CART 治疗分析中,约 30%的患者在接受 CART 治疗后 2 年仍存活且无进展。尽管复发率较高(2 年时为 69%),但这些结果表明,一部分 R/R THRLBCL 患者可能会对 CART 产生持久的反应。