Blinatumoab公司
医学
微小残留病
内科学
淋巴细胞白血病
造血干细胞移植
胃肠病学
急性淋巴细胞白血病
化疗
完全缓解
肿瘤科
白血病
疾病
作者
Nicola Gökbuget,Gerhard Zugmaier,Hervé Dombret,Anthony S. Stein,Massimiliano Bonifacio,Carlos Graux,Christoph Faul,Monika Brüggemann,Kate Taylor,Noemi Mergen,Albrecht Reichle,Heinz‐August Horst,Violaine Havelange,Max S. Topp,Ralf C. Bargou
标识
DOI:10.1080/10428194.2020.1780583
摘要
Minimal residual disease (MRD) is the strongest predictor of relapse in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). In BLAST study (NCT01207388), adults with BCP-ALL in remission with MRD after chemotherapy received blinatumomab, a CD19 BiTE® immuno-oncotherapy, 15 µg/m2/day for up to four 6-week cycles (4 weeks continuous infusion, 2 weeks off). Survival was evaluated for 110 patients, including 74 who received HSCT in continuous complete remission. With a median follow-up of 59·8 months, median survival (months) was 36·5 (95% CI: 22.0–not reached [NR]). Median survival was NR (29.5–NR) for complete MRD responders (n = 84) and 14.4 (3.8–32.3) for MRD non-responders (n = 23; p = 0.002); after blinatumomab and HSCT, median survival was NR (25.7–NR) (n = 61) and 16.5 (1.1–NR) (n = 10; p = 0.065), respectively. This final analysis suggests complete MRD response during blinatumomab treatment is curative. Post-hoc analysis of study data suggests while post blinatumomab HSCT may be beneficial in appropriate patients, long-term survival without HSCT is also possible.
科研通智能强力驱动
Strongly Powered by AbleSci AI