| Literature DB >> 30526152 |
Jorge Labrador1, Elisa Luño2, Edo Vellenga3, Salut Brunet4, José González-Campos5, Maria C Chillón6,7, Aleksandra Holowiecka8, Jordi Esteve9, Juan Bergua10, José D González-Sanmiguel11, Cristina Gil12, Mar Tormo13, Olga Salamero14, Felix Manso15, Isolda Fernández16, Javier de laSerna17, María-José Moreno18, Manuel Pérez-Encinas19, Isabel Krsnik20, Josep-Maria Ribera21, Jose Cervera22, María J Calasanz7,23,24, Blanca Boluda7,22, Marta Sobas25, Bob Lowenberg26, Miguel A Sanz7,22,27, Pau Montesinos7,22.
Abstract
Although additional cytogenetic abnormalities (ACA) do not affect the prognosis of patients with t(15;17) acute promyelocytic leukemia (APL), the role of a complex karyotype (CK) is yet to be clarified. We aimed to investigate the relationship of CK with relapse incidence in 1559 consecutive APL patients enrolled in three consecutive trials. Treatment consisted of AIDA induction followed by risk-adapted consolidation. A CK (CK) was defined as the presence of ≥2 ACA, and a very CK (CK+) as ≥3 ACA. Eighty-nine patients (8%) had a CK, of whom 41 (4%) had CK+. The 5-year cumulative incidence of relapse (CIR) in patients with CK was 18%, and 12% in those with <2 ACA (p=.09). Among patients with CK+, the 5-year CIR was 27% vs 12% (p=.003), retaining the statistical significance in multivariate analysis. This study shows an increased risk of relapse among APL patients with CK + treated with ATRA plus chemotherapy front-line regimens.Entities:
Keywords: ATRA; Acute promyelocytic leukemia; chemotherapy; complex karyotype; prognostic; relapse
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Year: 2018 PMID: 30526152 DOI: 10.1080/10428194.2018.1522438
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022