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Long-term follow-up of blinatumomab in patients with relapsed/refractory Philadelphia chromosome–positive B-cell precursor acute lymphoblastic leukaemia: Final analysis of ALCANTARA study

Blinatumoab公司 医学 肿瘤科 内科学 淋巴细胞白血病 儿科 耐火材料(行星科学) 白血病 生物 天体生物学
作者
Giovanni Martinelli,Nicolas Boissel,Patrice Chevallier,Oliver G. Ottmann,Nicola Gökbuget,Alessandro Rambaldi,Ellen K. Ritchie,Cristina Papayannidis,Catherine Tuglus,Joan Morris,Anthony S. Stein
出处
期刊:European Journal of Cancer [Elsevier BV]
卷期号:146: 107-114 被引量:91
标识
DOI:10.1016/j.ejca.2020.12.022
摘要

AIM: To evaluate long-term durability of blinatumomab, a BiTE® (bispecific T-cell engager) molecule, in adults with relapsed/refractory (R/R) Philadelphia chromosome-positive (Ph+) B-cell precursor acute lymphoblastic leukaemia (ALL). METHODS: In this final analysis of an open-label, single-arm, phase 2, multicentre ALCANTARA study (NCT02000427), adults (age ≥18 years) with Ph+ ALL who had relapsed or were refractory to at least one TKI were included. The primary endpoint was the proportion of patients who achieved complete remission (CR)/CR with partial haematologic recovery (CRh) during the first two cycles of blinatumomab treatment. RESULTS: The final analysis included 45 patients who completed the study between 3rd January 2014 and 6th January 2017, of which 16 (35.6%; 95% CI, 21.9%-51.2%) achieved CR/CRh within the first two blinatumomab cycles. After a median follow-up of 16.1 months, median relapse-free survival (RFS) was 6.8 (95% CI, 4.4-not estimable [NE]) months. Median overall survival (OS) was 9.0 (95% CI, 5.7-13.5) months with a median follow-up of 25.1 months. Median OS in patients with CR (19.8 [95% CI, 12.1-NE] months) was greater than in those without CR (6.0 [95% CI, 2.9-7.1] months). Of 16 patients with CR/CRh, 14 achieved complete minimal residual disease (MRD) response; the median duration of complete MRD response was 9.7 (95% CI, 5.2-NE) months. Treatment-related adverse events were consistent with those previously reported. CONCLUSION: Long-term durability of responses to blinatumomab was demonstrated in patients with R/R Ph+ ALL.
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