Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Medicine, Goethe University Hospital, Frankfurt, Germany.
Cancer. 2019 Dec 1;125(23):4181-4192. doi: 10.1002/cncr.32335. Epub 2019 Aug 21.
Blinatumomab, a bispecific T-cell-engaging (BiTE®) immuno-oncology therapy, demonstrated superior overall survival versus standard-of-care chemotherapy (SOC) in adults with relapsed/refractory B-cell precursor acute lymphoblastic leukemia (R/R ALL) in the phase 3 TOWER study. Herein, the authors reported clinical features and outcomes for those patients who underwent allogeneic hematopoietic stem cell transplantation (HSCT) after treatment with blinatumomab.
In the TOWER study, adults with R/R ALL were randomized 2:1 to receive blinatumomab or SOC. Study treatment consisted of 2 cycles of induction with blinatumomab or SOC followed by consolidation and maintenance therapy. At any time after the first cycle, patients who were eligible for HSCT could proceed to HSCT.
Of the 97 patients who underwent HSCT during the study, baseline characteristics generally were comparable and donor types were similar between the patients treated with blinatumomab (65 patients) and those receiving SOC (32 patients). There was no evidence to suggest that the survival benefit of HSCT differed between the patients treated with blinatumomab and those receiving SOC (P = .68). On the basis of descriptive statistics, a survival benefit of HSCT versus no HSCT was not observed in patients who achieved complete remission with full, partial, or incomplete hematologic recovery with blinatumomab (odds ratio, 1.17; 95% CI, 0.54-2.53). The best outcomes were achieved in patients with no prior salvage therapy and with minimal residual disease response to blinatumomab regardless of on-study HSCT status.
Survival was found to be driven by response to study treatment and by salvage status regardless of on-study HSCT status. These data should be interpreted with caution because the current study was not designed to prospectively assess survival outcomes associated with HSCT after blinatumomab.
Evidence before this study: Blinatumomab is associated with superior morphologic and molecular response rates and superior overall outcome when compared with standard of care chemotherapy in adults with relapsed/refractory B-cell precursor acute lymphoblastic leukemia. Added value of this study: The best outcomes with blinatumomab were observed in patients who achieved minimal residual disease remission in first salvage treatment regardless of subsequent allogeneic stem cell transplantation (HSCT). Implications of all the available evidence: Patients achieving CR/CRh/CRi following blinatumomab can have a durable response with or without HSCT.
blinatumomab 是一种双特异性 T 细胞接合(BiTE®)免疫肿瘤疗法,在复发/难治性 B 细胞前体急性淋巴细胞白血病(R/R ALL)成人患者中,与标准治疗化疗(SOC)相比,总生存期(OS)得到了显著改善。在这项 3 期 TOWER 研究中,作者报告了接受 blinatumomab 治疗后接受同种异体造血干细胞移植(HSCT)的患者的临床特征和结局。
在 TOWER 研究中,R/R ALL 成人患者按 2:1 随机分组接受 blinatumomab 或 SOC 治疗。研究治疗包括 2 个周期的诱导治疗,用 blinatumomab 或 SOC 治疗,然后进行巩固和维持治疗。在第一周期后的任何时间,有资格接受 HSCT 的患者都可以进行 HSCT。
在研究期间接受 HSCT 的 97 例患者中,基线特征总体上相似,接受 blinatumomab 治疗的患者(65 例)和接受 SOC 治疗的患者(32 例)的供体类型也相似。没有证据表明接受 blinatumomab 治疗的患者与接受 SOC 治疗的患者之间 HSCT 的生存获益存在差异(P=0.68)。基于描述性统计,在接受 blinatumomab 治疗后达到完全缓解(伴完全、部分或不完全血液学恢复)的患者中,HSCT 与不进行 HSCT 相比,生存获益没有观察到(比值比,1.17;95%置信区间,0.54-2.53)。在无既往挽救治疗且对 blinatumomab 有最小残留疾病反应的患者中,获得了最佳结局。
生存由对研究治疗的反应和挽救状况驱动,而与研究期间 HSCT 状态无关。这些数据应谨慎解读,因为本研究并非旨在前瞻性评估 blinatumomab 后 HSCT 与生存结局的相关性。
blinatumomab 与标准治疗化疗相比,可显著提高成人复发/难治性 B 细胞前体急性淋巴细胞白血病患者的形态学和分子反应率,并改善总体结局。
在首次挽救治疗中达到最小残留疾病缓解的患者,无论是否随后进行同种异体干细胞移植(HSCT),均可观察到 blinatumomab 的最佳结局。
接受 blinatumomab 治疗后达到完全缓解(伴完全、部分或不完全血液学恢复)的患者,HSCT 与不进行 HSCT 相比,生存获益没有观察到。