TY - JOUR
T1 - Achieving Molecular Remission before Allogeneic Stem Cell Transplantation in Adult Patients with Philadelphia Chromosome–Positive Acute Lymphoblastic Leukemia
T2 - Impact on Relapse and Long-Term Outcome
AU - Lussana, Federico
AU - Intermesoli, Tamara
AU - Gianni, Francesca
AU - Boschini, Cristina
AU - Masciulli, Arianna
AU - Spinelli, Orietta
AU - Oldani, Elena
AU - Tosi, Manuela
AU - Grassi, Anna
AU - Parolini, Margherita
AU - Audisio, Ernesta
AU - Cattaneo, Chiara
AU - Raimondi, Roberto
AU - Angelucci, Emanuele
AU - Cavattoni, Irene Maria
AU - Scattolin, Anna Maria
AU - Cortelezzi, Agostino
AU - Mannelli, Francesco
AU - Ciceri, Fabio
AU - Mattei, Daniele
AU - Borlenghi, Erika
AU - Terruzzi, Elisabetta
AU - Romani, Claudio
AU - Bassan, Renato
AU - Rambaldi, Alessandro
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Allogeneic stem cell transplantation (alloHSCT) in first complete remission (CR1) remains the consolidation therapy of choice in Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL). The prognostic value of measurable levels of minimal residual disease (MRD) at time of conditioning is a matter of debate. We analyzed the predictive relevance of MRD levels before transplantation on the clinical outcome of Ph+ ALL patients treated with chemotherapy and imatinib in 2 consecutive prospective clinical trials. MRD evaluation before transplantation was available for 65 of the 73 patients who underwent an alloHSCT in CR1. A complete or major molecular response at time of conditioning was achieved in 24 patients (37%), whereas 41 (63%) remained carriers of any other positive MRD level in the bone marrow. MRD negativity at time of conditioning was associated with a significant benefit in terms of risk of relapse at 5 years, with a relapse incidence of 8% compared with 39% for patients with MRD positivity (P = .007). However, thanks to the post-transplantation use of tyrosine kinase inhibitors (TKIs), disease-free survival was 58% versus 41% (P = .17) and overall survival was 58% versus 49% (P = .55) in MRD-negative compared with MRD-positive patients, respectively. The cumulative incidence of nonrelapse mortality was similar in the 2 groups. Achieving a complete molecular remission before transplantation reduces the risk of leukemia relapse even though TKIs may still rescue some patients relapsing after transplantation.
AB - Allogeneic stem cell transplantation (alloHSCT) in first complete remission (CR1) remains the consolidation therapy of choice in Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL). The prognostic value of measurable levels of minimal residual disease (MRD) at time of conditioning is a matter of debate. We analyzed the predictive relevance of MRD levels before transplantation on the clinical outcome of Ph+ ALL patients treated with chemotherapy and imatinib in 2 consecutive prospective clinical trials. MRD evaluation before transplantation was available for 65 of the 73 patients who underwent an alloHSCT in CR1. A complete or major molecular response at time of conditioning was achieved in 24 patients (37%), whereas 41 (63%) remained carriers of any other positive MRD level in the bone marrow. MRD negativity at time of conditioning was associated with a significant benefit in terms of risk of relapse at 5 years, with a relapse incidence of 8% compared with 39% for patients with MRD positivity (P = .007). However, thanks to the post-transplantation use of tyrosine kinase inhibitors (TKIs), disease-free survival was 58% versus 41% (P = .17) and overall survival was 58% versus 49% (P = .55) in MRD-negative compared with MRD-positive patients, respectively. The cumulative incidence of nonrelapse mortality was similar in the 2 groups. Achieving a complete molecular remission before transplantation reduces the risk of leukemia relapse even though TKIs may still rescue some patients relapsing after transplantation.
KW - Acute lymphoblastic leukemia
KW - Allogeneic transplantation
KW - Minimal residual disease (MRD)
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U2 - 10.1016/j.bbmt.2016.07.021
DO - 10.1016/j.bbmt.2016.07.021
M3 - Article
AN - SCOPUS:84992393687
SN - 1083-8791
VL - 22
SP - 1983
EP - 1987
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
IS - 11
ER -