Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, California.
Department of Computational and Quantitative Medicine, City of Hope National Medical Center, Duarte, California.
Cancer. 2022 Feb 1;128(3):529-535. doi: 10.1002/cncr.33967. Epub 2021 Oct 11.
Blinatumomab has demonstrated encouraging activity in relapsed/refractory (r/r) and minimal residual disease-positive (MRD+) acute lymphoblastic leukemia (ALL). Extramedullary disease (EMD) relapse or relapse with CD19- disease has been observed after blinatumomab therapy in patients with r/r or MRD+ ALL. However, the pathophysiology and risk factors of treatment failure are not fully understood.
This study retrospectively reviewed the outcomes of adult patients with B-cell ALL treated with blinatumomab (n = 132) for either r/r (n = 103) or MRD+ disease (n = 29) at the authors' center (2013-2021) and analyzed factors associated with treatment response and EMD failure.
The overall response rate was 64%. A lower marrow blast burden before blinatumomab (P = .049) and no history of previous EMD (P = .019) were significantly associated with a higher response. Among the patients who responded to blinatumomab, 56% underwent consolidation with allogeneic transplantation. Blinatumomab failure was observed in 89 patients; 43% of these patients (n = 38) either progressed or relapsed at extramedullary sites. A history of extramedullary involvement (53% vs 24%; P = .005) and retention of CD19 expression at the time of relapse/progression (97% vs 74%; P = .012) were associated with a higher risk for extramedullary failure. Central nervous system (CNS) failure after blinatumomab was encountered in 39% of the patients with EMD.
A history of EMD predicted an inferior response to blinatumomab therapy with a higher risk for relapse/progression at extramedullary sites (particularly CNS). Consolidation with allogenic transplantation in patients who primarily responded to blinatumomab did not abrogate the risk of extramedullary relapse. The incorporation of extramedullary assessment and the intensification of CNS prophylaxis may help in addressing extramedullary failure.
Extramedullary failure is common during blinatumomab therapy for relapsed/refractory acute lymphoblastic leukemia. A history of extramedullary disease predicts an inferior response to blinatumomab therapy and a higher risk for relapse/progression at extramedullary sites. Most extramedullary failure cases retain CD19 expression.
blinatumomab 在复发/难治性(r/r)和微小残留病灶阳性(MRD+)急性淋巴细胞白血病(ALL)患者中显示出令人鼓舞的疗效。在接受blinatumomab 治疗的 r/r 或 MRD+ALL 患者中,已经观察到骨髓外疾病(EMD)复发或伴有 CD19-疾病的复发。然而,治疗失败的病理生理学和危险因素尚未完全阐明。
本研究回顾性分析了作者中心 132 例接受blinatumomab 治疗的 B 细胞 ALL 患者(r/r103 例,MRD+29 例)的治疗结局(2013-2021 年),并分析了与治疗反应和 EMD 失败相关的因素。
总缓解率为 64%。blinatumomab 治疗前骨髓原始细胞比例较低(P=0.049)和无既往 EMD 史(P=0.019)与更高的缓解率显著相关。在blinatumomab 治疗缓解的患者中,56%接受了异基因移植巩固治疗。89 例患者blinatumomab 治疗失败;其中 43%(n=38)在髓外部位进展或复发。既往有髓外受累史(53%比 24%;P=0.005)和复发/进展时保留 CD19 表达(97%比 74%;P=0.012)与髓外失败风险增加相关。blinatumomab 治疗后 39%的 EMD 患者发生中枢神经系统(CNS)失败。
既往有 EMD 史预示着blinatumomab 治疗反应较差,髓外部位复发/进展风险较高(尤其是 CNS)。在主要对blinatumomab 治疗有反应的患者中进行异基因移植巩固治疗并不能消除髓外复发的风险。髓外评估的纳入和 CNS 预防的强化可能有助于解决髓外失败问题。
blinatumomab 治疗复发/难治性急性淋巴细胞白血病时,骨髓外失败较为常见。既往有骨髓外疾病史预示着blinatumomab 治疗反应较差,且髓外部位复发/进展风险较高。大多数骨髓外失败病例保留 CD19 表达。