Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2021 Jun 15;127(12):2025-2038. doi: 10.1002/cncr.33469. Epub 2021 Mar 19.
The outcome of patients with relapsed/refractory (R/R) acute lymphoblastic leukemia (ALL) is poor. The combination of inotuzumab with low-intensity mini-hyper-CVD (mini-hyper-CVD; cyclophosphamide and dexamethasone at 50% dose reduction, no anthracycline, methotrexate at 75% dose reduction, cytarabine at 0.5 g/m × 4 doses) chemotherapy has shown encouraging results. The sequential addition of blinatumomab might improve outcome in patients with R/R ALL.
We used lower intensity chemotherapy, mini-hyper-CVD (cyclophosphamide and dexamethasone at 50% dose reduction, no anthracycline, methotrexate at 75% dose reduction, cytarabine at 0.5 g/m x 4 doses) compared to conventional hyper-CVAD.
Ninety-six patients with a median age of 37 years (range, 18-87 years) were treated. Overall, 77 patients (80%) responded, 55 (57%) of whom achieved complete response. The overall measurable residual disease negativity rate among responders was 83%. Forty-four (46%) patients underwent later allogeneic stem cell transplantation. Veno-occlusive disease of any grade occurred in 10 (10%) patients. The rates were 13% with the original schedule and 3% with the use of lower-dose inotuzumab and sequential blinatumomab. With a median follow-up of 36 months, the median overall survival (OS) was 13.4 months, with 3-year OS rates of 33%. The 3-year OS rate for patients with CD22 expression ≥70% and without adverse cytogenetics (KMT2A rearrangements, low hypodiploidy/near triploidy) was 55%.
The combination of inotuzumab and low-intensity mini-hyper-CVD chemotherapy with or without blinatumomab shows sustained efficacy in patients with R/R ALL.
复发/难治性(R/R)急性淋巴细胞白血病(ALL)患者的预后较差。英妥昔单抗联合低强度 mini-hyper-CVD(mini-hyper-CVD;环磷酰胺和地塞米松剂量减少 50%,无蒽环类药物,甲氨蝶呤剂量减少 75%,阿糖胞苷 4 次 0.5g/m)化疗显示出令人鼓舞的结果。序贯添加blinatumomab可能改善 R/R ALL 患者的预后。
我们使用较低强度的化疗,mini-hyper-CVD(环磷酰胺和地塞米松剂量减少 50%,无蒽环类药物,甲氨蝶呤剂量减少 75%,阿糖胞苷 4 次 0.5g/m)与常规 hyper-CVAD 相比。
96 例患者中位年龄 37 岁(范围,18-87 岁)。总体而言,77 例患者(80%)有反应,55 例(57%)完全缓解。应答者的总可测量残留疾病阴性率为 83%。44 例(46%)患者随后接受异基因造血干细胞移植。任何级别的静脉闭塞性疾病在 10 例(10%)患者中发生。原始方案的发生率为 13%,低剂量英妥昔单抗和序贯blinatumomab的发生率为 3%。中位随访 36 个月,中位总生存期(OS)为 13.4 个月,3 年 OS 率为 33%。CD22 表达≥70%且无不良细胞遗传学(KMT2A 重排、低倍体/近三倍体)的患者 3 年 OS 率为 55%。
英妥昔单抗联合低强度 mini-hyper-CVD 化疗联合或不联合blinatumomab在 R/R ALL 患者中显示出持续的疗效。