Dasatinib/prednisone induction followed by blinatumomab/ dasatinib in Ph(+) acute lymphoblastic leukemia Journal Article


Authors: Advani, A. S.; Moseley, A.; O’Dwyer, K. M.; Wood, B. L.; Park, J.; Wieduwilt, M.; Jeyakumar, D.; Yaghmour, G.; Atallah, E. L.; Gerds, A. T.; O’Brien, S. M.; Liesveld, J. L.; Othus, M.; Litzow, M.; Stone, R. M.; Sharon, E.; Erba, H. P.
Article Title: Dasatinib/prednisone induction followed by blinatumomab/ dasatinib in Ph(+) acute lymphoblastic leukemia
Abstract: 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. © 2023 American Society of Hematology. All rights reserved.
Journal Title: Blood Advances
Volume: 7
Issue: 7
ISSN: 2473-9529
Publisher: American Society of Hematology  
Date Published: 2023-04-11
Start Page: 1279
End Page: 1285
Language: English
DOI: 10.1182/bloodadvances.2022008216
PUBMED: 36322825
PROVIDER: scopus
PMCID: PMC10090098
DOI/URL:
Notes: Article -- Export Date: 1 June 2023 -- Source: Scopus
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  1. Jae Hong Park
    357 Park