Barlev Arie, Lin Vincent W, Katz Aaron, Hu Kuolung, Cong Ze, Barber Beth
Global Health Economics, Amgen Inc., Thousand Oaks, CA, USA.
Center for Observational Research, Amgen Inc., Thousand Oaks, CA, USA.
Adv Ther. 2017 Jan;34(1):148-155. doi: 10.1007/s12325-016-0447-x. Epub 2016 Nov 21.
Blinatumomab is a bispecific T cell-engaging antibody construct indicated for adult patients with relapsed/refractory (R/R) Ph(-) B-precursor acute lymphoblastic leukemia (ALL), an aggressive disease with poor prognosis. A phase 2 single-arm clinical study showed that 43% of patients achieved CR/CRh within two cycles and approximately 20% of patients receiving blinatumomab were still alive after 2 years.
The objective of the current analysis was to estimate long-term survival of patients receiving blinatumomab beyond the observed time period in the clinical study using a large historical observational dataset. Conditional survival probabilities of blinatumomab-treated patients beyond month 60 were assumed to be the same as the US general population.
At month 60, the estimated proportion of blinatumomab-treated patients alive was more than double that of historical patients (12.6% vs 5.4%). The mean overall survival was 76.1 months for blinatumomab patients and 39.8 months for historical patients. Sensitivity analyses including additional follow-up data from the clinical study showed consistent results.
These findings suggest that blinatumomab provides substantial overall survival benefit to patients with (R/R) Ph(-) B-precursor ALL compared with salvage chemotherapy.
Amgen.
ClinicalTrials.gov identifier NCT01466179 and NCT02003612.
博纳吐单抗是一种双特异性T细胞衔接抗体构建体,适用于复发/难治性(R/R)Ph(-) B前体急性淋巴细胞白血病(ALL)的成年患者,这是一种预后不良的侵袭性疾病。一项2期单臂临床研究表明,43%的患者在两个周期内达到完全缓解/完全缓解伴血液学不完全恢复(CR/CRh),接受博纳吐单抗治疗的患者中约20%在2年后仍然存活。
本次分析的目的是使用一个大型历史观察数据集,估计在临床研究观察期之后接受博纳吐单抗治疗的患者的长期生存率。假设接受博纳吐单抗治疗的患者在60个月后的条件生存概率与美国普通人群相同。
在60个月时,接受博纳吐单抗治疗的存活患者估计比例是历史患者的两倍多(12.6%对5.4%)。博纳吐单抗治疗患者的平均总生存期为76.1个月,历史患者为39.8个月。包括来自临床研究的额外随访数据的敏感性分析显示了一致的结果。
这些发现表明,与挽救性化疗相比,博纳吐单抗为(R/R)Ph(-) B前体ALL患者提供了显著的总生存获益。
安进公司。
ClinicalTrials.gov标识符NCT01466179和NCT02003612。