Title | US Intergroup Study of Chemotherapy Plus Dasatinib and Allogeneic Stem Cell Transplant in Philadelphia Chromosome Positive ALL. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Ravandi, F, Othus, M, O'Brien, SM, Forman, SJ, Ha, CS, Wong, JYC, Tallman, MS, Paietta, E, Racevskis, J, Uy, GL, Horowitz, M, Takebe, N, Little, R, Borate, U, Kebriaei, P, Kingsbury, L, Kantarjian, HM, Radich, JP, Erba, HP, Appelbaum, FR |
Journal | Blood Adv |
Volume | 1 |
Issue | 3 |
Pagination | 250-259 |
Date Published | 2016 Dec 27 |
ISSN | 2473-9529 |
Abstract | This multicenter trial was conducted to determine whether the addition of dasatinib to chemotherapy followed by an allogeneic hematopoietic cell transplant (HCT) in patients with Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia (ALL) was feasible. Patients ≥ 18 and ≤ 60 years of age with newly diagnosed Ph+ ALL received up to 8 cycles of alternating hyperCVAD and high dose cytarabine and methotrexate with dasatinib. Patients with an available matched sibling or unrelated donor underwent an allogeneic HCT in first complete remission (CR1) followed by daily dasatinib starting from day 100. Others received maintenance therapy with vincristine and prednisone for 2 years and dasatinib indefinitely. 97 patients (94 evaluable) with median age of 44 years (range, 20 - 60) and median WBC at presentation of 10 × 10/L (range, 1 - 410 × 10/L) were accrued. 83 (88%) patients achieved CR or CR with incomplete count recovery (CRi) and 41 underwent ASCT in CR1. Median follow-up is 36 months (range, 9 - 63). For the overall population, overall survival (OS), event-free survival (EFS), and relapse-free survival (RFS) at 3 years were 69%, 55%, and 62%, respectively. The 12-month RFS and OS after transplant were 71% and 87%, respectively. Landmark analysis at 175 days from the time of CR/CRi (longest time to HCT), showed statistically superior advantages for RFS and OS (p=0.038 and 0.037, respectively) for the transplanted patients. Addition of dasatinib to chemotherapy and HCT for younger patients with Ph+ ALL is feasible and warrants further testing. |
DOI | 10.1182/bloodadvances.2016001495 |
Alternate Journal | Blood Adv |
PubMed ID | 29046900 |
PubMed Central ID | PMC5642915 |
Grant List | U10 CA004919 / CA / NCI NIH HHS / United States U24 CA196172 / CA / NCI NIH HHS / United States UG1 HL069278 / HL / NHLBI NIH HHS / United States U10 HL109137 / HL / NHLBI NIH HHS / United States U10 CA180818 / CA / NCI NIH HHS / United States U10 CA180820 / CA / NCI NIH HHS / United States U10 CA011083 / CA / NCI NIH HHS / United States U10 CA046368 / CA / NCI NIH HHS / United States U10 CA180888 / CA / NCI NIH HHS / United States U10 CA180816 / CA / NCI NIH HHS / United States N01 CA004919 / CA / NCI NIH HHS / United States U10 HL069294 / HL / NHLBI NIH HHS / United States U10 CA012644 / CA / NCI NIH HHS / United States P30 CA016672 / CA / NCI NIH HHS / United States N01 CA013612 / CA / NCI NIH HHS / United States U10 HL069278 / HL / NHLBI NIH HHS / United States U24 CA076518 / CA / NCI NIH HHS / United States U10 CA013612 / CA / NCI NIH HHS / United States U10 CA180835 / CA / NCI NIH HHS / United States U10 CA180821 / CA / NCI NIH HHS / United States U10 CA180801 / CA / NCI NIH HHS / United States U10 CA180858 / CA / NCI NIH HHS / United States UG1 CA189848 / CA / NCI NIH HHS / United States U10 CA180846 / CA / NCI NIH HHS / United States U10 CA046282 / CA / NCI NIH HHS / United States U01 HL069294 / HL / NHLBI NIH HHS / United States U10 CA180819 / CA / NCI NIH HHS / United States UG1 CA189953 / CA / NCI NIH HHS / United States |