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:CAR T in patients with large B-cell lymphoma not fit for autologous transplant.
CAR T in patients with large B-cell lymphoma not fit for autologous transplant.
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合并症和/或高龄大B细胞淋巴瘤患者越来越多考虑CD19 CAR-T,但较不适合强化治疗人群的临床获益数据有限。本研究按自体干细胞移植(ASCT)适合度分析英国国家CAR-T 临床小组批准接受阿基仑赛或替沙仑赛患者结局。404名获批患者中81名(20%)不适合ASCT。不适合者更常接受替沙仑赛而非阿基仑赛(52%比48%);ASCT适合者分别为20%和80%(p<0.0001)。不适合组从获批到输注的脱落率更高(34.6%比23.5%,p=0.042)。在实际输注者中,两组缓解率、PFS和OS相似。不适合ASCT患者对CAR-T 耐受良好,3级CRS和神经毒性发生率分别为2%和11%。该多中心真实世界队列显示,经谨慎选择后,CAR-T 可安全用于不适合移植的老年及合并症患者。
Large B-cell lymphoma (LBCL) patients with comorbidities and/or advanced age are increasingly considered for treatment with CD19 CAR T, but data on the clinical benefit of CAR T in the less fit patient population are still limited.
We analysed outcomes of consecutive patients approved for treatment with axicabtagene ciloleucel (axi-cel) or tisagenlecleucel (tisa-cel) by the UK National CAR T Clinical Panel, according to fitness for autologous stem cell transplant (ASCT). 81/404 (20%) of approved patients were deemed unfit for ASCT. Unfit patients were more likely to receive tisa-cel versus axi-cel (52% vs. 48%) compared to 20% versus 80% in ASCT-fit patients; p < 0. 0001. The drop-out rate from approval to infusion was significantly higher in the ASCT-unfit group (34.
6% vs. 23. 5%; p = 0. 042). Among infused patients, response rate, progression-free and overall survival were similar in both cohorts. CAR T was well-tolerated in ASCT-unfit patients with an incidence of grade 3 cytokine release syndrome and neurotoxicity of 2% and 11%, respectively. Results from this multicentre real-world cohort demonstrate that CD19 CAR T can be safely delivered in carefully selected older patients and patients with comorbidities who are not deemed suitable for transplant.
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