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:Collection efficiency and safety of large-volume leukapheresis for the manufacturing of tisagenlecleucel.
Collection efficiency and safety of large-volume leukapheresis for the manufacturing of tisagenlecleucel.
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使用 Spectra Optia cMNC 方案进行的 LVL 操作耐受性良好,且未影响 tisa-cel 的制备。
在复发/难治性B细胞急性淋巴细胞白血病或B细胞非霍奇金淋巴瘤(r/r B-ALL/B-NHL)患者中,若外周血(PB)CD3+细胞较低,采用常规容量白细胞单采术(NVL)可能无法在单日内获得足够的CD3+细胞产量。大容量白细胞单采术(LVL)是指在单次PB单采中处理超过总血容量(TBV)三倍的血液;然而,LVL用于制备tisagenlecleucel(tisa-cel)的效率与安全性仍不明确。本研究旨在探讨LVL的耐受性。研究设计与方法:我们回顾性收集了2019年11月至2023年9月期间在本机构为r/r B-ALL/B-NHL患者实施的LVL(≥3倍TBV)和NVL(<3倍TBV)数据。所有操作均使用Spectra Optia采用连续单个核细胞采集(cMNC)方案进行。
尽管在LVL操作中,PB中采集前CD3+细胞显著较低(900 vs. 348/μL,p < .01),但所有患者均可在单日内获得足够的CD3+细胞产量,两组最终产品(包括不符合规格)的成功率相当(97.2% vs. 100.0%,p = 1.00)。操作期间柠檬酸盐毒性的发生率和严重程度(无患者≥3级)在两组间无显著差异(22.2% vs. 26.1%,p = .43),且无患者因任何并发症中止白细胞分离术。
In patients with relapsed or refractory B cell acute lymphoblastic leukemia or B cell non-Hodgkin lymphoma (r/r B-ALL/B-NHL) with low CD3 + cells in the peripheral blood (PB), sufficient CD3 + cell yield in a single day may not be obtained with normal-volume leukapheresis (NVL). Large-volume leukapheresis (LVL) refers to the processing of more than three times the total blood volume (TBV) in a single session for PB apheresis; however, the efficiency and safety of LVL for manufacturing of tisagenlecleucel (tisa-cel) remain unclear. This study aimed to investigate the tolerability of LVL. STUDY DESIGN AND METHODS: We retrospectively collected data on LVL (≥3-fold TBV) and NVL (<3-fold TBV) performed for patients with r/r B-ALL/B-NHL in our institution during November 2019 and September 2023. All procedures were performed using a continuous mononuclear cell collection (cMNC) protocol with the Spectra Optia.
Although pre-apheresis CD3 + cells in the PB were significantly lower in LVL procedures (900 vs. 348/μL, p < .01), all patients could obtain sufficient CD3 + cell yield in a single day with a comparably successful rate of final products (including out-of-specification) between the two groups (97.2% vs. 100.0%, p = 1.00). The incidence and severity of citrate toxicity (no patients with grade ≥ 3) during procedures was not significantly different between the two groups (22.2% vs. 26.1%, p = .43) and no patient discontinued leukapheresis due to any complications.
LVL procedures using Spectra Optia cMNC protocol was well tolerated and did not affect the manufacturing of tisa-cel.
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