The poor prognosis of low hypodiploidy in adults with B-cell precursor acute lymphoblastic leukaemia is restricted to older adults and elderly patients.
Jordi RiberaIsabel GranadaMireia MorgadesSusana VivesEulàlia GenescàCelia GonzálezJosep NomdedeuLourdes EscodaPau MontesinosSantiago MercadalRosa CollJosé González-CamposEugenia AbellaPere BarbaArancha BermúdezCristina GilMar TormoMaría PedreñoDaniel Martínez-CarballeiraJesús-María Hernández-RivasAlberto OrfaoJoaquin Martinez LopezJordi EstevePilar BravoAntoni Garcia-GuiñonGuillermo DebénJosé M MoraledaJosé A QueizánXavier OrtínMaría J MorenoEvarist FeliuFrancesc SoléJosep M Riberanull nullPublished in: British journal of haematology (2019)
The prognostic significance of low-hypodiploidy has not been extensively evaluated in minimal residual disease (MRD)-oriented protocols for adult acute lymphoblastic leukaemia (ALL). We analysed the outcome of hypodiploid adult ALL patients treated within Programa Español de Tratamientos en Hematología (PETHEMA) protocols. The 5-year cumulative incidence of relapse (CIR) of low-hypodiploid B-cell precursor (BCP)-ALL was significantly higher than that of high-hypodiploids (52% vs. 12%, P = 0.013). Low-hypodiploid BCP-ALL patients aged ≤35 years showed superior survival (71% vs. 21%, P = 0.026) and lower 5-year CIR (17% vs. 66%, P = 0.090) than low-hypodiploids aged >35 years. Older adults and elderly low-hypodiploid BCP-ALL patients show dismal prognosis although achieving an end-induction good MRD response.