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Dasatinib/prednisone induction followed by blinatumomab/dasatinib in Ph+ acute lymphoblastic leukemia.
Advani, Anjali S; Moseley, Anna; O'Dwyer, Kristen M; Wood, Brent L; Park, Jae; Wieduwilt, Matthew; Jeyakumar, Deepa; Yaghmour, George; Atallah, Ehab L; Gerds, Aaron T; O'Brien, Susan M; Liesveld, Jane L; Othus, Megan; Litzow, Mark; Stone, Richard M; Sharon, Elad; Erba, Harry P.
Afiliação
  • Advani AS; Cleveland Clinic/Taussig Cancer Center, Cleveland, OH.
  • Moseley A; SWOG Statistics and Data Management Center, Seattle, WA.
  • O'Dwyer KM; Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Wood BL; University of Rochester/James P. Wilmot Cancer Institute, Rochester, NY.
  • Park J; Departments of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.
  • Wieduwilt M; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Jeyakumar D; University of California San Diego Moores Cancer Center, La Jolla, CA.
  • Yaghmour G; UC Irvine Medical Center, Orange, CA.
  • Atallah EL; USC Norris Comprehensive Cancer Center, Los Angeles, CA.
  • Gerds AT; Froedtert and the Medical College of Wisconsin, Milwaukee, WI.
  • O'Brien SM; Cleveland Clinic/Taussig Cancer Center, Cleveland, OH.
  • Liesveld JL; UC Irvine Medical Center, Orange, CA.
  • Othus M; University of Rochester/James P. Wilmot Cancer Institute, Rochester, NY.
  • Litzow M; SWOG Statistics and Data Management Center, Seattle, WA.
  • Stone RM; Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Sharon E; Division of Hematology, Mayo Clinic, Rochester, MN.
  • Erba HP; Dana-Farber Cancer Institute, Boston, MA.
Blood Adv ; 7(7): 1279-1285, 2023 04 11.
Article em En | MEDLINE | ID: mdl-36322825
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Limite: Aged / Aged80 / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Limite: Aged / Aged80 / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article