决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Inotuzumab ozogamicin as single agent in pediatric patients with relapsed and refractory acute lymphoblastic leukemia: results from a phase II trial.
Inotuzumab ozogamicin as single agent in pediatric patients with relapsed and refractory acute lymphoblastic leukemia: results from a phase II trial.
年龄 1-18 岁、R/R CD22⁺ BCP-ALL 患者按 RP2D 1.8 mg/m² 接受治疗。
伊诺妥珠单抗奥唑米星是一种靶向CD22、偶联卡奇霉素的抗体,已获批用于成人复发/难治性(R/R)B细胞前体急性淋巴细胞白血病(BCP-ALL)。本研究纳入1至18岁、患R/R CD22阳性BCP-ALL的患者,按推荐Ⅱ期剂量(RP2D)1.8 mg/m²治疗。采用单阶段设计,将总缓解率(ORR)≤30%定义为不具前景,ORR>55%定义为预期疗效;在显著性水平0.05下,需招募25例患者以达到80%把握度。共入组32例,28例接受治疗,27例可评估疗效。估计ORR为81.5%(95%置信区间[CI]:61.9%~93.7%);应答者中18/22(81.8%)达到微小残留病(MRD)阴性。研究达到主要终点。存活者中位随访16个月(四分位距:14.49~20.07)。1年无事件生存率为36.7%(95% CI:22.2%~60.4%),总生存率为55.1%(95% CI:39.1%~77.7%)。18例患者接受巩固治疗(造血干细胞移植和/或CAR-T细胞治疗)。7例发生窦状隙阻塞综合征(SOS)。MRD阴性似乎与体外卡奇霉素敏感性相关,但与CD22表面表达、饱和度或内化无关。伊诺妥珠单抗在该人群中有效;最重要的风险是SOS,尤其是在伊诺妥珠单抗治疗后进行造血干细胞移植时。
Inotuzumab Ozogamicin is a CD22-directed antibody conjugated to calicheamicin, approved in adults with relapsed or refractory (R/R) B cell acute lymphoblastic leukemia (BCP-ALL). Patients aged 1-18 years, with R/R CD22 + BCP-ALL were treated at the RP2D of 1.8 mg/m 2 . Using a single-stage design, with an overall response rate (ORR) 30% defined as not promissing and ORR > 55% as expected, 25 patients needed to be recruited to achieve 80% power at 0.05 significance level. Thirty-two patients were enrolled, 28 were treated, 27 were evaluable for response. The estimated ORR was 81.5% (95%CI: 61.9-93.7%), and 81.8% (18/22) of the responding subjects were minimal residual disease (MRD) negative. The study met its primary endpoint. Median follow up of survivors was 16 months (IQR: 14.49-20.07). One year Event Free Survival was 36.7% (95% CI: 22.2-60.4%), and Overall Survival was 55.1% (95% CI: 39.1-77.7%). Eighteen patients received consolidation (with HSCT and/or CAR T-cells therapy). Sinusoidal obstructive syndrome (SOS) occurred in seven patients. MRD negativity seemed correlated to calicheamicin sensitivity in vitro, but not to CD22 surface expression, saturation, or internalization. InO was effective in this population. The most relevant risk was the occurrence of SOS, particularly when InO treatment was followed by HSCT.
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