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Chemotherapy or allogeneic transplantation in high-risk Philadelphia chromosome-negative adult lymphoblastic leukemia.
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.
Affiliation
  • Ribera JM; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Morgades M; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Ciudad J; Instituto de Investigación Biomédica de Salamanca (IBSAL), Instituto de Biología Molecular y Celular del Cáncer (IBMCC), Centro de Investigación del Cáncer, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Universidad de Salamanca-Centro Superior de Investigaciones Científicas (CSIC),
  • Montesinos P; Department of Hematology, Hospital Universitario La Fe, Valencia, Spain.
  • Esteve J; Department of Hematology, Hospital Clínic, Institut D'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
  • Genescà E; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Barba P; Department of Hematology, Hospital Vall d'Hebron, Barcelona, Spain.
  • Ribera J; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • García-Cadenas I; Department of Hematology, Hospital de Sant Pau, Barcelona, Spain.
  • Moreno MJ; Department of Hematology, Hospital Virgen de la Victoria, Málaga, Spain.
  • Martínez-Carballeira D; Department of Hematology, Hospital Central de Asturias, Oviedo, Spain.
  • Torrent A; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Martínez-Sánchez P; Department of Hematology, Hospital Doce de Octubre, Madrid, Spain.
  • Monsalvo S; Department of Hematology, Hospital Gregorio Marañón, Madrid, Spain.
  • Gil C; Department of Hematology, Hospital General, Alicante, Spain.
  • Tormo M; Department of Hematology, Hospital Clínico, Instituto de Investigación INCLIVA, Valencia, Spain.
  • Artola MT; Department of Hematology, Hospital Universitario, Donostia, Spain.
  • Cervera M; Institut Català d'Oncologia-Hospital Joan XXIII, Tarragona, Spain.
  • González-Campos J; Department of Hematology, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
  • Rodríguez C; Department of Hematology, Hospital Doctor Negrín, Las Palmas de Gran Canaria, Spain.
  • Bermúdez A; Department of Hematology, Hospital Marqués de Valdecilla, Santander, Spain.
  • Novo A; Department of Hematology, Hospital Son Espases, Palma de Mallorca, Spain.
  • Soria B; Department of Hematology, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.
  • Coll R; Institut Català d'Oncologia-Hospital Josep Trueta, Girona, Spain.
  • Amigo ML; Department of Hematology, Hospital Morales Meseguer, Murcia, Spain.
  • López-Martínez A; Department of Hematology, Hospital Arnau de Vilanova, Valencia, Spain.
  • Fernández-Martín R; Department of Hematology, Hospital Universitario Insular, Las Palmas de Gran Canaria, Spain.
  • Serrano J; Department of Hematology, Hospital Reina Sofía, Córdoba, Spain.
  • Mercadal S; Institut Català d'Oncologia-Hospital Duran i Reynals, L'Hospitalet de Llobregat, Spain.
  • Cladera A; Department of Hematology, Hospital Son Llàtzer, Palma de Mallorca, Spain.
  • Giménez-Conca A; Department of Hematology, Hospital Italiano, Buenos Aires, Argentina.
  • Peñarrubia MJ; Department of Hematology, Hospital Clínico, Valladolid, Spain.
  • Abella E; Department of Hematology, Hospital del Mar, Barcelona, Spain.
  • Vall-Llovera F; Department of Hematology, Hospital Universitari Mútua, Terrassa, Spain.
  • Hernández-Rivas JM; Instituto de Investigación Biomédica de Salamanca (IBSAL), Instituto de Biología Molecular y Celular del Cáncer (IBMCC), Centro de Investigación del Cáncer, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Universidad de Salamanca-Centro Superior de Investigaciones Científicas (CSIC),
  • Garcia-Guiñon A; Department of Hematology, Hospital Arnau de Vilanova, Lleida, Spain.
  • Bergua JM; Department of Hematology, Hospital San Pedro de Alcántara, Cáceres, Spain.
  • de Rueda B; Department of Hematology, Hospital Miguel Servet, Zaragoza, Spain.
  • Sánchez-Sánchez MJ; Department of Hematology, Hospital Lucus Augusti, Lugo, Spain.
  • Serrano A; Department of Hematology, Hospital HM Sanchinarro, Madrid, Spain.
  • Calbacho M; Department of Hematology, Hospital Ramón y Cajal, Madrid, Spain.
  • Alonso N; Department of Hematology, Hospital Clínico, Santiago de Compostela, Spain.
  • Méndez-Sánchez JÁ; Department of Hematology, Complejo Hospitalario, Ourense, Spain.
  • García-Boyero R; Department of Hematology, Hospital General, Castellón, Spain.
  • Olivares M; Department of Hematology, Hospital Universitario, Galdakao, Spain; and.
  • Barrena S; Instituto de Investigación Biomédica de Salamanca (IBSAL), Instituto de Biología Molecular y Celular del Cáncer (IBMCC), Centro de Investigación del Cáncer, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Universidad de Salamanca-Centro Superior de Investigaciones Científicas (CSIC),
  • Zamora L; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Granada I; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Lhermitte L; Université de Paris, Institut Necker-Enfants Malades, Institut National de Recherche Médicale U1151, Laboratory of Onco-Hematology, Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants-Malades, Paris, France.
  • Feliu E; Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain.
Blood ; 137(14): 1879-1894, 2021 04 08.
Article in En | MEDLINE | ID: mdl-33150388
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Precursor Cell Lymphoblastic Leukemia-Lymphoma Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Precursor Cell Lymphoblastic Leukemia-Lymphoma Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2021 Document type: Article Affiliation country:
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