Department of Lymphoma and Myeloma.
Department of Biostatistics, and.
Blood Adv. 2022 May 10;6(9):2867-2871. doi: 10.1182/bloodadvances.2021006715.
About 70% of patients with large B-cell lymphoma (LBCL) who are treated with axicabtagene ciloleucel (axi-cel) and who achieve a partial response (PR) or stable disease (SD) on the day 30 (D30) positron emission tomography (PET)-computed tomography (CT) scan progress; however, the factors that are predictive of progression are unknown. This a retrospective study of patients with LBCL who were treated with axi-cel at MD Anderson Cancer Center between January of 2018 and February of 2021. Among 50 patients with D30 PR/SD, 13 (26%) converted to a complete response (CR). Among 95 patients with a D30 CR, 72 (76%) remained in CR. On univariate analysis, the only day -5 characteristic associated with conversion from D30 PR/SD to subsequent CR was a higher platelet count (P = .05). The only D30 factor associated with conversion from D30 PR/SD to subsequent CR was a lower maximum standardized uptake volume (SUVmax; P < .001); all patients with D30 SUVmax ≥ 10 progressed. After a median follow-up of 12 months, no significant difference in median progression-free survival was observed between patients who converted from D30 PR/SD to subsequent CR and those who had been in CR since D30 (P = .19). Novel predictive and prognostic markers based on tissue biopsy and noninvasive diagnostic assays are needed to more effectively identify these patients and characterize the biology of their residual disease.
约 70%接受 axi-cel 治疗且在第 30 天(D30)正电子发射断层扫描(PET)-计算机断层扫描(CT)检查中达到部分缓解(PR)或稳定疾病(SD)的大 B 细胞淋巴瘤(LBCL)患者会进展;然而,目前尚不清楚哪些因素具有预测进展的作用。这是一项回顾性研究,纳入了 2018 年 1 月至 2021 年 2 月期间在 MD 安德森癌症中心接受 axi-cel 治疗的 LBCL 患者。在 50 例 D30 PR/SD 的患者中,有 13 例(26%)转化为完全缓解(CR)。在 95 例 D30 CR 的患者中,有 72 例(76%)保持 CR。在单因素分析中,与从 D30 PR/SD 转为后续 CR 相关的唯一 D-5 特征是血小板计数较高(P=0.05)。与从 D30 PR/SD 转为后续 CR 相关的唯一 D30 因素是最大标准化摄取值(SUVmax)较低(P<0.001);所有 D30 SUVmax≥10 的患者均进展。中位随访 12 个月后,从 D30 PR/SD 转为后续 CR 的患者与从 D30 起即保持 CR 的患者的中位无进展生存期无显著差异(P=0.19)。需要基于组织活检和非侵入性诊断检测的新型预测和预后标志物,以更有效地识别这些患者并对其残留疾病的生物学特性进行表征。