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

Author:

Ribera Josep-Maria1ORCID,Morgades Mireia1ORCID,Ciudad Juana2,Montesinos Pau3ORCID,Esteve Jordi4ORCID,Genescà Eulàlia1ORCID,Barba Pere5,Ribera Jordi1,García-Cadenas Irene6,Moreno María José7,Martínez-Carballeira Daniel8,Torrent Anna1,Martínez-Sánchez Pilar9,Monsalvo Silvia10,Gil Cristina11,Tormo Mar12,Artola María Teresa13,Cervera Marta14,González-Campos José15,Rodríguez Carlos16,Bermúdez Arancha17,Novo Andrés18,Soria Beatriz19,Coll Rosa20ORCID,Amigo María-Luz21,López-Martínez Aurelio22,Fernández-Martín Rosa23,Serrano Josefina24,Mercadal Santiago25,Cladera Antònia26,Giménez-Conca Alberto27,Peñarrubia María-Jesús28,Abella Eugènia29,Vall-llovera Ferran30ORCID,Hernández-Rivas Jesús-María2,Garcia-Guiñon Antoni31,Bergua Juan-Miguel32ORCID,de Rueda Beatriz33,Sánchez-Sánchez María-José34ORCID,Serrano Alfons35,Calbacho María36ORCID,Alonso Natalia37,Méndez-Sánchez Jose-Ángel38,García-Boyero Raimundo39,Olivares Matxalen40,Barrena Susana2,Zamora Lurdes1,Granada Isabel1ORCID,Lhermitte Ludovic41,Feliu Evarist1,Orfao Alberto2

Affiliation:

1. Institut Català d’Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain;

2. 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), Hospital Universitario, Salamanca, Spain;

3. Department of Hematology, Hospital Universitario La Fe, Valencia, Spain;

4. Department of Hematology, Hospital Clínic, Institut D'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain;

5. Department of Hematology, Hospital Vall d’Hebron, Barcelona, Spain;

6. Department of Hematology, Hospital de Sant Pau, Barcelona, Spain;

7. Department of Hematology, Hospital Virgen de la Victoria, Málaga, Spain;

8. Department of Hematology, Hospital Central de Asturias, Oviedo, Spain;

9. Department of Hematology, Hospital Doce de Octubre, Madrid, Spain;

10. Department of Hematology, Hospital Gregorio Marañón, Madrid, Spain;

11. Department of Hematology, Hospital General, Alicante, Spain;

12. Department of Hematology, Hospital Clínico, Instituto de Investigación INCLIVA, Valencia, Spain;

13. Department of Hematology, Hospital Universitario, Donostia, Spain;

14. Institut Català d’Oncologia-Hospital Joan XXIII, Tarragona, Spain;

15. Department of Hematology, Hospital Universitario Virgen del Rocío, Sevilla, Spain;

16. Department of Hematology, Hospital Doctor Negrín, Las Palmas de Gran Canaria, Spain;

17. Department of Hematology, Hospital Marqués de Valdecilla, Santander, Spain;

18. Department of Hematology, Hospital Son Espases, Palma de Mallorca, Spain;

19. Department of Hematology, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain;

20. Institut Català d’Oncologia-Hospital Josep Trueta, Girona, Spain;

21. Department of Hematology, Hospital Morales Meseguer, Murcia, Spain;

22. Department of Hematology, Hospital Arnau de Vilanova, Valencia, Spain;

23. Department of Hematology, Hospital Universitario Insular, Las Palmas de Gran Canaria, Spain;

24. Department of Hematology, Hospital Reina Sofía, Córdoba, Spain;

25. Institut Català d’Oncologia-Hospital Duran i Reynals, L’Hospitalet de Llobregat, Spain;

26. Department of Hematology, Hospital Son Llàtzer, Palma de Mallorca, Spain;

27. Department of Hematology, Hospital Italiano, Buenos Aires, Argentina;

28. Department of Hematology, Hospital Clínico, Valladolid, Spain;

29. Department of Hematology, Hospital del Mar, Barcelona, Spain;

30. Department of Hematology, Hospital Universitari Mútua, Terrassa, Spain;

31. Department of Hematology, Hospital Arnau de Vilanova, Lleida, Spain;

32. Department of Hematology, Hospital San Pedro de Alcántara, Cáceres, Spain;

33. Department of Hematology, Hospital Miguel Servet, Zaragoza, Spain;

34. Department of Hematology, Hospital Lucus Augusti, Lugo, Spain;

35. Department of Hematology, Hospital HM Sanchinarro, Madrid, Spain;

36. Department of Hematology, Hospital Ramón y Cajal, Madrid, Spain;

37. Department of Hematology, Hospital Clínico, Santiago de Compostela, Spain;

38. Department of Hematology, Complejo Hospitalario, Ourense, Spain;

39. Department of Hematology, Hospital General, Castellón, Spain;

40. Department of Hematology, Hospital Universitario, Galdakao, Spain; and

41. 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

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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