A phase 3 trial of azacitidine versus a semi-intensive fludarabine and cytarabine schedule in older patients with untreated acute myeloid leukemia

Año de publicación
2021
Autores
Vives, S; Martinez-Cuadron, D; Burgues, JB; Algarra, L; Tormo, M; Martinez-Sanchez, MP; Serrano, J; Herrera, P; Ramos, F; Salamero, O; Lavilla, E; Lopez-Lorenzo, JL; Gil, C; Vidriales, B; Falantes, JF; Serrano, A; Labrador, J; Sayas, MJ; Foncillas, MA; Barciela, MLA; Olave, MT; Colorado, M; Gascon, A; Fernandez, MA; Simiele, A; Perez-Encinas, MM; Rodriguez-Veiga, R; Garcia, O; Martinez-Lopez, J; Barragan, E; Paiva, B; Sanz, MA; Montesinos, P
Grupo de Trabajo
Revista
CANCER
Volumen
127
Start page
2003
End page
2014
Issue
12

BACKGROUND Options to treat elderly patients (>= 65 years old) newly diagnosed with acute myeloid leukemia (AML) include intensive and attenuated chemotherapy, hypomethylating agents with or without venetoclax, and supportive care. This multicenter, randomized, open-label, phase 3 trial was designed to assess the efficacy and safety of a fludarabine, cytarabine, and filgrastim (FLUGA) regimen in comparison with azacitidine (AZA). METHODS Patients (n = 283) were randomized 1:1 to FLUGA (n = 141) or AZA (n = 142).

Response was evaluated after cycles 1, 3, 6, and 9. Measurable residual disease (MRD) was assessed after cycle 9. When MRD was >= 0.01%, patients continued with the treatment until relapse or progressive disease. Patients with MRD < 0.01% suspended treatment to enter the follow-up phase. RESULTS The complete remission (CR) rate after 3 cycles was significantly better in the FLUGA arm (18% vs 9%; P = .04), but the CR/CR with incomplete recovery rate at 9 months was similar (33% vs 29%; P = .41).

There were no significant differences between arms in early mortality at 30 or 60 days. Hematologic toxicities were more frequent with FLUGA, especially during induction.

The 1-year overall survival (OS) rate and the median OS were superior with AZA versus FLUGA: 47% versus 27% and 9.8 months (95% confidence interval [CI], 5.6-14 months) versus 4.1 months (95% CI, 2.7-5.5 months; P = .005), respectively.

The median event-free survival was 4.9 months (95% CI, 2.8-7 months) with AZA and 3 months (95% CI, 2.5-3.5 months) with FLUGA (P = .001).

CONCLUSIONS FLUGA achieved more remissions after 3 cycles, but the 1-year OS rate was superior with AZA.

However, long-term outcomes were disappointing in both arms (3-year OS rate, 10% vs 5%).

This study supports the use of an AZA backbone for future combinations in elderly patients with AML.