Causes and prognostic factors of remission induction failure in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and idarubicin

J de la Serna, P Montesinos, E Vellenga, C Rayon, R Parody, A Leon, J Esteve, JM Bergua, G Milone, G Deben, C Rivas, M Gonzalez, M Tormo, J Diaz-Mediavilla, JD Gonzalez, S Negri, E Amutio, S Brunet, Bob Löwenberg, MA Sanz

Research output: Contribution to journalArticleAcademicpeer-review

266 Citations (Scopus)

Abstract

An understanding of the prognostic factors associated with the various forms of induction mortality in patients with acute promyelocytic leukemia (APL) has remained remarkably limited. This study reports the incidence, time of occurrence, and prognostic factors of the major categories of induction failure in a series of 732 patients of all ages (range, 2-83 years) with newly diagnosed APL who received all-trans retinoic acid (ATRA) plus idarubicin as induction therapy in 2 consecutive studies of the Programa de Estudio y Tratamiento de las Hemopatias Malignas (PETHEMA) Group. Complete remission was attained in 666 patients (91%). All the 66 induction failures were due to induction death. Hemorrhage was the most common cause of induction death (5%), followed by infection (2.3%) and differentiation syndrome (1.4%). Multivariate analysis identified specific and distinct pretreatment characteristics to correlate with an increased risk of death caused by hemorrhage (abnormal creatinine level, increased peripheral blast counts, and presence of coagulopathy), infection (age >60 years, male sex, and fever at presentation), and differentiation syndrome (Eastern Cooperative Oncology Group [ECOG] score >1 and low albumin levels), respectively. These data furnish clinically relevant information that might be useful for designing more appropriately risk-adapted treatment protocols aimed at reducing the considerable problem of induction mortality in APL.
Original languageUndefined/Unknown
Pages (from-to)3395-3402
Number of pages8
JournalBlood
Volume111
Issue number7
DOIs
Publication statusPublished - 2008

Cite this