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

移植 急性淋巴细胞白血病 肿瘤科 布苏尔班 淋巴细胞白血病 白血病 环磷酰胺 甲氨蝶呤 微小残留病
作者
Josep‐Marǐa Ribera,Mireia Morgades,Juana Ciudad,Pau Montesinos,Jordi Esteve,Eulàlia Genescà,Pere Barba,Irene García‐Cadenas,Marı́a José Moreno,Daniel Martínez‐Carballeira,Anna Torrent,Pilar Martínez‐Sánchez,Silvia Monsalvo,Cristina Gil,Mar Tormo,María Teresa Artola,Marta Cervera,José González‐Campos,Carlos Rodríguez,Arancha Bermúdez,Andrés Novo,Beatriz Yolanda Moratilla Soria,Rosa Coll,María‐Luz Amigo,Aurelio López-Martínez,Rosa Fernández-Martín,Josefina Serrano,Santiago Mercadal,Antònia Cladera,Alberto Giménez‐Conca,María-Jesús Peñarrubia,Eugènia Abella,Ferran Vall‐Llovera,Jesús‐María Hernández‐Rivas,Antoni García‐Guiñón,Juan-Miguel Bergua,Beatriz De Rueda,María‐José Sánchez‐Sánchez,Alfons Serrano,M. Calbacho,Natalia Alonso,Jose-Ángel Méndez-Sánchez,Raimundo García‐Boyero,Matxalen Olivares,Susana Bárrena,Lurdes Zamora,Isabel Granada,Ludovic Lhermitte,Evarist Feliú,Alberto Órfão
出处
期刊:Blood [Elsevier BV]
卷期号:137 (14): 1879-1894 被引量:42
标识
DOI:10.1182/blood.2020007311
摘要

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.gov as # NCT01540812.
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