| Literature DB >> 28987821 |
Giuseppe Visani1, Felicetto Ferrara2, Francesco Di Raimondo3, Federica Loscocco4, Fabio Fuligni5, Stefania Paolini5, Valentina Zammit3, Eleonora Spina3, Marco Rocchi6, Axel Visani5, Pier Paolo Piccaluga7, Alessandro Isidori4.
Abstract
Outcome for elderly patients with acute myeloid leukemia (AML) is extremely poor. Intensive induction chemotherapy is often unsuitable. Sixty-six newly diagnosed AML patients (median age: 76years), ineligible for standard therapy, were consecutively treated with low-dose lenalidomide (10mg/day orally, days 1-21) plus 10mg/m2 low-dose cytarabine, subcutaneously, twice a day (days 1-15) every six weeks, up to 6 cycles. Complete remission (CR) rate was 36.3% according to intention-to-treat. Responding patients had a longer median overall survival than non-responders (517 vs. 70days, P<0.001). The achievement of CR was not predicted by bone marrow blast count, cytogenetics, molecular markers, prior MDS, white blood cell count. Conversely, by studying the global gene expression profile, we identified a molecular signature, including 309 genes associated with clinical response (CR versus no CR). Based on the expression of a minimal set of 16 genes, we developed an algorithm to predict treatment response, that was successfully validated by showing an overall accuracy of 88%. We met the primary endpoint of the study, by beating the estimated successful CR rate (P1) fixed at 30%. Moreover, CR induced by this 2-drug combo was efficiently predicted by genetic profiling, identifying a biomarker that warrants validation in independent series.Entities:
Keywords: Acute myeloid leukemia; Biomarker; Complete remission; Elderly; Gene expression profile; Low-dose therapy; Unfit
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Year: 2017 PMID: 28987821 DOI: 10.1016/j.leukres.2017.09.019
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156