不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Long-term outcomes of patients with large B-cell lymphoma treated with axicabtagene ciloleucel and prophylactic corticosteroids.
Long-term outcomes of patients with large B-cell lymphoma treated with axicabtagene ciloleucel and prophylactic corticosteroids.
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ZUMA-1安全性管理队列6研究了预防性使用皮质类固醇及早期使用皮质类固醇和/或tocilizumab对复发/难治性大B细胞淋巴瘤(R/R LBCL)患者接受axicabtagene ciloleucel(axi-cel)治疗后细胞因子释放综合征(CRS)和神经系统事件(NEs)发生率及严重程度的影响。队列6的既往分析随访时间有限,显示无≥3级CRS、NEs发生率低、缓解率高,且未对axi-cel药代动力学产生负面影响。本文报告队列6(N = 40)的长期结局(中位随访时间26.9个月)。自1年分析(Oluwole等,Blood. 2022;138[增刊1]:2832)以来,未报告新的CRS。2例患者发生2起新发NEs(2级痴呆,与axi-cel无关;5级白质脑病,与axi-cel相关)。发生6起新发感染和8例死亡(5例疾病进展;1例白质脑病;2例COVID-19)。客观缓解率和完全缓解率分别维持在95%和80%。中位缓解持续时间和无进展生存期分别为25.9个月和26.8个月。中位总生存期尚未达到。数据截止时,18例患者(45%)仍处于持续缓解中。随访≥2年,预防性使用皮质类固醇及早期使用皮质类固醇和/或tocilizumab持续显示CRS改善,且未影响疗效结局,疗效仍然高且持久。
ZUMA-1 safety management cohort 6 investigated the impact of prophylactic corticosteroids and earlier corticosteroids and/or tocilizumab on the incidence and severity of cytokine release syndrome (CRS) and neurologic events (NEs) following axicabtagene ciloleucel (axi-cel) in patients with relapsed/refractory large B-cell lymphoma (R/R LBCL). Prior analyses of cohort 6 with limited follow-up demonstrated no Grade ≥3 CRS, a low rate of NEs, and high response rates, without negatively impacting axi-cel pharmacokinetics.
Herein, long-term outcomes of cohort 6 (N = 40) are reported (median follow-up, 26. 9 months). Since the 1-year analysis (Oluwole, et al. Blood. 2022;138[suppl 1]:2832), no new CRS was reported. Two new NEs occurred in two patients (Grade 2 dementia unrelated to axi-cel; Grade 5 axi-cel-related leukoencephalopathy). Six new infections and eight deaths (five progressive disease; one leukoencephalopathy; two COVID-19) occurred. Objective and complete response rates remained at 95% and 80%, respectively.
Median duration of response and progression-free survival were reached at 25. 9 and 26. 8 months, respectively. Median overall survival has not yet been reached. Eighteen patients (45%) remained in ongoing response at data cutoff. With ≥2 years of follow-up, prophylactic corticosteroids and earlier corticosteroids and/or tocilizumab continued to demonstrate CRS improvement without compromising efficacy outcomes, which remained high and durable.
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