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Chemotherapy or allogeneic transplantation in high-risk Philadelphia chromosome–negative adult lymphoblastic leukemia

Authors :
Ribera, Josep-Maria
Morgades, Mireia
Ciudad, Juana
Montesinos, Pau
Esteve, Jordi
Genescà, Eulàlia
Barba, Pere
Ribera, Jordi
García-Cadenas, Irene
Moreno, María José
Martínez-Carballeira, Daniel
Torrent, Anna
Martínez-Sánchez, Pilar
Monsalvo, Silvia
Gil, Cristina
Tormo, Mar
Artola, María Teresa
Cervera, Marta
González-Campos, José
Rodríguez, Carlos
Bermúdez, Arancha
Novo, Andrés
Soria, Beatriz
Coll, Rosa
Amigo, María-Luz
López-Martínez, Aurelio
Fernández-Martín, Rosa
Serrano, Josefina
Mercadal, Santiago
Cladera, Antònia
Giménez-Conca, Alberto
Peñarrubia, María-Jesús
Abella, Eugènia
Vall-llovera, Ferran
Hernández-Rivas, Jesús-María
Garcia-Guiñon, Antoni
Bergua, Juan-Miguel
de Rueda, Beatriz
Sánchez-Sánchez, María-José
Serrano, Alfons
Calbacho, María
Alonso, Natalia
Méndez-Sánchez, Jose-Ángel
García-Boyero, Raimundo
Olivares, Matxalen
Barrena, Susana
Zamora, Lurdes
Granada, Isabel
Lhermitte, Ludovic
Feliu, Evarist
Orfao, Alberto
Source :
Blood; April 2021, Vol. 137 Issue: 14 p1879-1894, 16p
Publication Year :
2021

Abstract

The need for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in adults with Philadelphia chromosome–negative (Ph−) acute lymphoblastic leukemia (ALL) with high-risk (HR) features and adequate measurable residual disease (MRD) clearance remains unclear. The aim of the ALL-HR-11 trial was to evaluate the outcomes of HR Ph−adult ALL patients following chemotherapy or allo-HSCT administered based on end-induction and consolidation MRD levels. Patients aged 15 to 60 years with HR-ALL in complete response (CR) and MRD levels (centrally assessed by 8-color flow cytometry) <0.1% after induction and <0.01% after early consolidation were assigned to receive delayed consolidation and maintenance therapy up to 2 years in CR. The remaining patients were allocated to allo-HSCT. CR was attained in 315/348 patients (91%), with MRD <0.1% after induction in 220/289 patients (76%). By intention-to-treat, 218 patients were assigned to chemotherapy and 106 to allo-HSCT. The 5-year (±95% confidence interval) cumulative incidence of relapse (CIR), overall survival (OS), and event-free survival probabilities for the whole series were 43% ± 7%, 49% ± 7%, and 40% ± 6%, respectively, with CIR and OS rates of 45% ± 8% and 59% ± 9% for patients assigned to chemotherapy and of 40% ± 12% and 38% ± 11% for those assigned to allo-HSCT, respectively. Our results show that avoiding allo-HSCT does not hamper the outcomes of HR Ph−adult ALL patients up to 60 years with adequate MRD response after induction and consolidation. Better postremission alternative therapies are especially needed for patients with poor MRD clearance. This trial was registered at www.clinicaltrials.govas # NCT01540812.

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
137
Issue :
14
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs55779835
Full Text :
https://doi.org/10.1182/blood.2020007311