| Literature DB >> 26492205 |
Farhad Ravandi1, Jeffrey L Jorgensen2, Susan M O'Brien1, Elias Jabbour1, Deborah A Thomas1, Gautam Borthakur1, Rebecca Garris1, Xuelin Huang3, Guillermo Garcia-Manero1, Jan A Burger1, Alessandra Ferrajoli1, William Wierda1, Tapan Kadia1, Nitin Jain1, Sa A Wang2, Sergei Konoplev2, Partow Kebriaei4, Richard E Champlin4, Deborah McCue5, Zeev Estrov1, Jorge E Cortes1, Hagop M Kantarjian1.
Abstract
The prognostic value of minimal residual disease (MRD) assessed by multi-parameter flow cytometry (MFC) was investigated among 340 adult patients with B-cell acute lymphoblastic leukaemia (B-ALL) treated between 2004 and 2014 using regimens including the hyperCVAD (hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone, methotrexate, cytarabine) backbone. Among them, 323 (95%) achieved complete remission (CR) and were included in this study. Median age was 52 years (range, 15-84). Median white blood cell count (WBC) was 9·35 × 10(9) /l (range, 0·4-658·1 ×1 0(9) /l). MRD by MFC was initially assessed with a sensitivity of 0·01%, using a 15-marker, 4-colour panel and subsequently a 6-colour panel on bone marrow specimens obtained at CR achievement and at approximately 3 month intervals thereafter. MRD negative status at CR was associated with improved disease-free survival (DFS) and overall survival (OS) (P = 0·004 and P = 0·03, respectively). Similarly, achieving MRD negative status at approximately 3 and 6 months was associated with improved DFS (P = 0·004 and P < 0·0001, respectively) and OS (P = 0·004 and P < 0·0001, respectively). Multivariate analysis including age, WBC at presentation, cytogenetics (standard versus high risk) and MRD status at CR, 3 and 6 months, indicated that MRD negative status at CR was an independent predictor of DFS (P < 0·05). Achievement of an MRD negative state assessed by MFC is an important predictor of DFS and OS in adult patients with ALL.Entities:
Keywords: acute leukaemia; flow cytometry; minimal residual disease
Mesh:
Year: 2015 PMID: 26492205 PMCID: PMC4826052 DOI: 10.1111/bjh.13834
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998