TY - JOUR
T1 - Molecular profiling refines minimal residual disease-based prognostic assessment in adults with Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia
AU - Ribera, Jordi
AU - Zamora, Lurdes
AU - Morgades, Mireia
AU - Vives, Susana
AU - Granada, Isabel
AU - Montesinos, Pau
AU - Gómez-Seguí, Inés
AU - Mercadal, Santiago
AU - Guàrdia, Ramon
AU - Nomdedeu, Josep
AU - Pratcorona, Marta
AU - Tormo, Mar
AU - Martínez-Lopez, Joaquín
AU - Hernández-Rivas, Jesús María
AU - Ciudad, Juana
AU - Orfao, Alberto
AU - González-Campos, José
AU - Barba, Pere
AU - Escoda, Lourdes
AU - Esteve, Jordi
AU - Genescà, Eulàlia
AU - Solé, Francesc
AU - Feliu, Evarist
AU - Ribera, Josep Maria
PY - 2019/11/1
Y1 - 2019/11/1
N2 - © 2019 Wiley Periodicals, Inc. Minimal residual disease (MRD) assessment is an essential tool in contemporary acute lymphoblastic leukemia (ALL) protocols, being used for therapeutic decisions such as hematopoietic stem cell transplantation in high-risk patients. However, a significant proportion of adult ALL patients with negative MRD still relapse suggesting that other factors (ie, molecular alterations) must be considered in order to identify those patients with high risk of disease progression. We have identified partial IKZF1 gene deletions and CDKN2A/B deletions as markers of disease recurrence and poor survival in a series of uniformly treated adolescent and adult Philadelphia chromosome-negative B-cell progenitor ALL patients treated according to the Programa Español de Tratamientos en Hematología protocols. Importantly, CDKN2A/B deletions showed independent significance of MRD at the end of induction, which points out the need for treatment intensification in these patients despite being MRD-negative after induction therapy.
AB - © 2019 Wiley Periodicals, Inc. Minimal residual disease (MRD) assessment is an essential tool in contemporary acute lymphoblastic leukemia (ALL) protocols, being used for therapeutic decisions such as hematopoietic stem cell transplantation in high-risk patients. However, a significant proportion of adult ALL patients with negative MRD still relapse suggesting that other factors (ie, molecular alterations) must be considered in order to identify those patients with high risk of disease progression. We have identified partial IKZF1 gene deletions and CDKN2A/B deletions as markers of disease recurrence and poor survival in a series of uniformly treated adolescent and adult Philadelphia chromosome-negative B-cell progenitor ALL patients treated according to the Programa Español de Tratamientos en Hematología protocols. Importantly, CDKN2A/B deletions showed independent significance of MRD at the end of induction, which points out the need for treatment intensification in these patients despite being MRD-negative after induction therapy.
UR - http://www.mendeley.com/research/molecular-profiling-refines-minimal-residual-diseasebased-prognostic-assessment-adults-philadelphia
U2 - 10.1002/gcc.22788
DO - 10.1002/gcc.22788
M3 - Article
C2 - 31340073
SN - 1045-2257
VL - 58
SP - 815
EP - 819
JO - Genes Chromosomes and Cancer
JF - Genes Chromosomes and Cancer
ER -