Dasatinib/prednisone induction followed by blinatumomab/dasatinib in Ph+ acute lymphoblastic leukemia

被引:31
作者
Advani, Anjali S. [1 ,16 ]
Moseley, Anna [2 ,3 ]
O'Dwyer, Kristen M. [4 ]
Wood, Brent L. [5 ,6 ]
Park, Jae [7 ]
Wieduwilt, Matthew [8 ]
Jeyakumar, Deepa [9 ]
Yaghmour, George [10 ]
Atallah, Ehab L. [11 ]
Gerds, Aaron T. [1 ]
O'Brien, Susan M. [9 ]
Liesveld, Jane L. [4 ]
Othus, Megan [2 ,3 ]
Litzow, Mark [12 ]
Stone, Richard M. [13 ]
Sharon, Elad [14 ]
Erba, Harry P. [15 ]
机构
[1] Cleveland Clin, Taussig Canc Ctr, Cleveland, OH USA
[2] SWOG Stat & Data Management Ctr, Seattle, WA USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA USA
[4] Univ Rochester, James P Wilmot Canc Inst, Rochester, NY USA
[5] Univ Washington, Dept Lab Med, Seattle, WA USA
[6] Univ Washington, Dept Pathol, Seattle, WA USA
[7] Mem Sloan Kettering Canc Ctr, New York, NY USA
[8] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA USA
[9] UC Irvine, Med Ctr, Orange, CA USA
[10] USC Norris Comprehens Canc Ctr, Los Angeles, CA USA
[11] Froedtert & Med Coll Wisconsin, Milwaukee, WI USA
[12] Mayo Clin, Div Hematol, Rochester, MN USA
[13] Dana Farber Canc Inst, Boston, MA USA
[14] NCI, Canc Therapy Evaluat Program, Bethesda, MD USA
[15] Duke Univ, Med Ctr, Durham, NC USA
[16] Cleveland Clin, Dept Hematol Oncol, Desk CA60,10201 Carnegie Ave, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
MINIMAL RESIDUAL DISEASE;
D O I
10.1182/bloodadvances.2022008216
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Novel treatment strategies are needed for the treatment of Philadelphia chromosome- positive (Ph+) acute lymphoblastic leukemia (ALL) in older patients. This trial evaluated the feasibility and outcomes with the anti-CD19 bispecific T-cell-engaging antibody, blinatumomab, in combination with dasatinib and steroids. Patients 65 years of age or older with Ph+ or Ph-like ALL (with dasatinib-sensitive fusions/mutations) were eligible and could be newly diagnosed or relapsed/refractory. Induction therapy consisted of dasatinib/ prednisone. Patients not achieving response by day 56 proceeded to blinatumomab reinduction therapy. Patients achieving response with induction or reinduction therapy proceeded to blinatumomab/dasatinib postremission therapy for 3 cycles followed by dasatinib/prednisone maintenance. All patients received central nervous system prophylaxis with intrathecal methotrexate for a total of 8 doses. Response was assessed at days 28, 56, and 84 and at additional time points based on response parameters. Measurable residual disease was assessed centrally by 8-color flow cytometry at day 28. A total of 24 eligible patients with newly diagnosed Ph+ ALL were enrolled with a median age of 73 years (range, 65-87 years). This combination was safe and feasible. With a median of 2.7 years of follow-up, 3-year overall survival and disease-free survival were 87% (95% confidence interval [CI], 64-96) and 77% (95% CI, 54-90), respectively. Although longer follow-up is needed, these results are encouraging, and future trials are building on this backbone regimen. This trial was registered at www.clinicaltrials.gov as #NCT02143414.
引用
收藏
页码:1279 / 1285
页数:7
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