Treatment patterns and outcomes of 2310 patients with secondary acute myeloid leukemia: a PETHEMA registry study

Author:

Martínez-Cuadrón David1ORCID,Megías-Vericat Juan Eduardo2ORCID,Serrano Josefina3,Martínez-Sánchez Pilar4,Rodríguez-Arbolí Eduardo5,Gil Cristina6,Aguiar Eliana7,Bergua Burgues Juan Miguel8ORCID,Lopez-Lorenzo Jose L9,Bernal Teresa10,Espadana Ana11,Colorado Mercedes12,Rodríguez-Medina Carlos13,López-Pavia María14,Tormo Mar15,Algarra Jesus Lorenzo16,Amigo Maria Luz17,Sayas Maria Jose18,Labrador Jorge19,Rodríguez-Gutiérrez Juan I.20,Benavente Celina21ORCID,Costilla-Barriga Lissette22ORCID,García-Boyero Raimundo23,lavilla esperanza24ORCID,Vives Susana25,Herrera Pilar26,García Daniel27ORCID,Herráez-Albendea María Mar28,Esteves Graça V29,Gómez-Roncero María Isabel30,Cabello Ana31,Bautista Guiomar32,Balerdi Amaia33,Mariz José34ORCID,Boluda Blanca1,Sanz Miguel A.1,Montesinos Pau1ORCID

Affiliation:

1. Instituto de Investigación Sanitaria La Fe (IISLAFE), Spain

2. Hospital Universitari i Politècnic La Fe, Valencia, Spain

3. University Hospital Reina Sofia. IMIBIC, Cordoba, Spain

4. Hospital Doce de Octubre, Madrid, Spain

5. Hospital Universitario Virgen del Rocío, Sevilla, Spain

6. Hospital Alicante, alicante, Spain

7. Dept. of Clinical Hematology, Centro Hospitalar Universitário São João, Porto, Portugal

8. Hospital San Pedro de Alcántara. Cáceres, Caceres, Spain

9. Fundacion Jimenez Diaz, Madrid, Spain

10. Hopsital Universitario Central Asturias, oviedo, Spain

11. Centro Hospitalar e Universitário de Coimbra, EPE, Coimbra, Portugal

12. Hospital Universitario Marqués de Valdecilla, Santander, Spain

13. Hospital Universitario de Gran Canaria Doctor Negrín, Las Palmas de Gran Canaria, Spain

14. Hospital General Universitario de Valencia, Valencia, Spain

15. Hospital Clinico Universitary. INCLIVA Research Institute, Valencia 46010, Spain

16. Hospital General de Albacete, Albacete, Spain

17. Hospital Morales Meseguer, Murcia, Spain

18. University Hospital Dr Peset, VALENCIA, Spain

19. Hospital Universitario de Burgos, Burgos, Spain

20. Universitario de Basurto, Bizkaia, Spain

21. Hospital Clínico San Carlos, Madrid, Spain

22. Hospital Miguel Servet, Zaragoza, Spain

23. Hospital General Universitario de Castellón, Castellón, Spain

24. Hospital Lucus Augusti, Lugo, Spain

25. José Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain, Spain

26. Hospital Ramon y Cajal, Madrid, Spain

27. Hospital Sanitas La Zarzuela, Spain

28. Hospital Santa Bárbara de Puertollano, Ciudad Real, Spain

29. Hospital de Santa Maria-Centro Hospitalar Lisboa Norte, Lisboa, Portugal

30. Hospital Virgen de la Salud, Toledo, Spain

31. Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain

32. Hospital Universitario Puerta de Hierro, Majadahonda, Spain

33. Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain

34. Portuguese Oncology Institute, maia, Portugal

Abstract

Secondary acute myeloid leukemia (sAML) comprises a heterogeneous group of patients, and is associated with poor overall survival (OS). We analyze the characteristics, treatment patterns and outcomes of sAML adult patients of the Programa Español de Tratamientos en Hematología (PETHEMA) registry. Overall, 6211 (72.9%) were de novo and 2310 (27.1%) sAML, divided into myelodysplastic syndrome (MDS-AML, 44%), MDS/myeloproliferative (MDS/MPN-AML, 10%), MPN-AML (11%), therapy-related (t-AML, 25%), and antecedent neoplasia without prior chemotherapy/radiotherapy (neo-AML, 9%). Compared to de novo, sAML were older (median age 69 years old), had more ECOG ≥2 (35%) or high-risk cytogenetics (40%), less FLT3-ITD (11%) and NPM1 mutations (21%), and received less intensive chemotherapy regimens (38%) (all P<0.001). Median OS was higher in de novo than in sAML (10.9 vs 5.6 months, P<0.001); and shorter in sAML after hematologic disorder (MDS, MDS/MPN or MPN) as compared to t-AML and neo-AML (5.3 vs 6.1 vs 5.7 months, respectively, P=0.04). After intensive chemotherapy, median OS was better among de novo and neo-AML patients (17.2 and 14.6 months). No OS differences were observed after hypomethylating agents according to type of AML. sAML was as an independent adverse prognostic factor for OS. We confirm high prevalence and adverse features of sAML and we establish its independent adverse prognostic value. This study was registered at www.clinicaltrials.gov as #NCT02607059.

Publisher

American Society of Hematology

Subject

Hematology

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