Outcome of patients with relapsed/refractory acute lymphoblastic leukemia after blinatumomab failure: No change in the level of CD19 expression

被引:70
作者
Jabbour, Elias [1 ]
Duell, Johannes [2 ]
Yilmaz, Musa [1 ]
Khoury, Joseph D. [3 ]
Ravandi, Farhad [1 ]
Jain, Nitin [1 ]
Einsele, Hermann [2 ]
Garcia-Manero, Guillermo [1 ]
Konopleva, Marina [1 ]
Short, Nicholas J. [1 ]
Thompson, Philip A. [1 ]
Wierda, William [1 ]
Daver, Naval [1 ]
Cortes, Jorge [1 ]
O'brien, Susan [4 ]
Kantarjian, Hagop [1 ]
Topp, Max S. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, 1515 Holcombe Blvd,Unit 428, Houston, TX 77030 USA
[2] Univ Klinikum Wurzburg, Med Klin & Poliklin 2, Wurzburg, Germany
[3] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
[4] Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Orange, CA 92668 USA
关键词
MINIMAL RESIDUAL DISEASE; T-CELL THERAPY; INOTUZUMAB OZOGAMICIN; ADULT PATIENTS; REMISSIONS; RESISTANCE; ANTIBODY; PHASE-2;
D O I
10.1002/ajh.24987
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Blinatumomab, a bi-specific T-cell engaging CD3-CD19 antibody construct, has shown significant activity in patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (ALL). Despite this improvement, most patients relapse. Here, we describe the outcome of 68 patients with R/R ALL after failure of blinatumomab therapy: 38 (56%) blinatumomab refractory; 30 (44%) relapsing after initial response. After a median follow-up of 49 months, 9 (13%) patients remained alive. The median overall survival after blinatumomab failure was 5.2 months. At the time of failure, among 61 patients evaluated for immunophenotype, 56 (92%) had CD19-positive blasts; only five (8%) had ALL recurrence with CD19-negative disease. Two patients progressed with lower CD19 expression. In summary, the outcome of patients with R/R ALL after blinatumomab failure is poor and treatment of these patients remains an unmet medical need. Our findings indicate that blinatumomab therapy would not exclude a significant number of patients from the potential benefit of subsequent CD19-directed therapies such as chimeric antigen receptor T-cell therapy.
引用
收藏
页码:371 / 374
页数:4
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