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在复发/难治性费城染色体阴性急性淋巴细胞白血病中,采用英妥昔单抗奥佐米星联合 mini-hyper-CVD 与或不联合blinatumomab 进行挽救性治疗的长期随访。

Long-term follow-up of salvage therapy using a combination of inotuzumab ozogamicin and mini-hyper-CVD with or without blinatumomab in relapsed/refractory Philadelphia chromosome-negative acute lymphoblastic leukemia.

机构信息

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.

出版信息

Cancer. 2021 Jun 15;127(12):2025-2038. doi: 10.1002/cncr.33469. Epub 2021 Mar 19.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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%.

CONCLUSION

The combination of inotuzumab and low-intensity mini-hyper-CVD chemotherapy with or without blinatumomab shows sustained efficacy in patients with R/R ALL.

摘要

背景

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。

方法

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。

结果

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%。

结论

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。

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