CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Day 30 SUVmax predicts progression in patients with lymphoma achieving PR/SD after CAR T-cell therapy.
Day 30 SUVmax predicts progression in patients with lymphoma achieving PR/SD after CAR T-cell therapy.
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接受axicabtagene ciloleucel(axi-cel)治疗的大B细胞淋巴瘤(LBCL)患者中,约70%在第30天(D30)正电子发射断层显像-计算机断层扫描(PET-CT)显示部分缓解(PR)或疾病稳定(SD),但随后出现进展;目前尚不清楚哪些因素能够预测进展。
本研究回顾性分析了2018年1月至2021年2月在MD Anderson癌症中心接受axi-cel治疗的LBCL患者。50例D30时为PR/SD的患者中,13例(26%)随后转为完全缓解(CR);95例D30时已达到CR的患者中,72例(76%)持续维持CR。单因素分析显示,与D30 PR/SD患者之后转为CR相关的唯一治疗前第5天特征是较高的血小板计数(P=0.05);唯一相关的D30因素则是较低的最大标准摄取值(SUVmax;P<0.001)。所有D30 SUVmax≥10的患者均出现进展。中位随访12个月后,D30时PR/SD而后转为CR的患者与D30时即为CR的患者之间,无进展生存期中位数没有显著差异(P=0.19)。仍需开发基于组织活检和无创诊断检测的新型预测及预后标志物,以更有效地识别这些患者并阐明其残留病灶的生物学特征。
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.
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