Curative outcomes following blinatumomab in adults with minimal residual disease B-cell precursor acute lymphoblastic leukemia

被引:55
|
作者
Goekbuget, Nicola [1 ]
Zugmaier, Gerhard [2 ]
Dombret, Herve [3 ]
Stein, Anthony [4 ]
Bonifacio, Massimiliano [5 ]
Graux, Carlos [6 ]
Faul, Christoph [7 ,8 ]
Brueggemann, Monika [9 ]
Taylor, Kate [10 ]
Mergen, Noemi [2 ]
Reichle, Albrecht [11 ]
Horst, Heinz-August [9 ]
Havelange, Violaine [12 ]
Topp, Max S. [13 ]
Bargou, Ralf C. [14 ]
机构
[1] Univ Hosp, D-60590 Frankfurt, Germany
[2] Amgen Res Munich GmbH, Munich, Germany
[3] Univ Paris, Univ Hop St Louis, AP HP, Paris, France
[4] City Hope Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
[5] Verona Univ, Dept Med, Sect Hematol, Verona, Italy
[6] Catholic Univ Louvain, CHU UCL Namur, Site Godinne, Yvoir, Belgium
[7] Univ Klinikum Tubingen, Univ Hosp, Tubingen, Germany
[8] Univ Klinikum Tubingen, Comprehens Canc Ctr Tubingen, Tubingen, Germany
[9] Univ Klinikum Schleswig Holstein, Klin Innere Med 2, Kiel, Germany
[10] Amgen Ltd, Cambridge, England
[11] Univ Hosp Regensburg, Dept Hematol & Oncol, Regensburg, Germany
[12] Clin Univ St Luc, Dept Hematol, Brussels, Belgium
[13] Univ Klinikum Wurzburg, Med Klin & Poliklin 2, Wurzburg, Germany
[14] Uniklinikum Wurzburg, Comprehens Canc Ctr Mainfranken, Wurzburg, Germany
关键词
Acute lymphoblastic leukemia; minimal residual disease; allogeneic hematopoietic stem cell transplantation; blinatumomab; immuno-oncotherapy; STANDARD-RISK; TRANSPLANTATION; MRD; QUANTIFICATION; REMISSION; THERAPY; RELAPSE; BLOOD;
D O I
10.1080/10428194.2020.1780583
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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(R)immuno-oncotherapy, 15 mu g/m(2)/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 center dot 8 months, median survival (months) was 36 center dot 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.
引用
收藏
页码:2665 / 2673
页数:9
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