TY - JOUR
T1 - Venetoclax-based combinations for acute myeloid leukemia
T2 - optimizing their use in Latin-America
AU - Gómez-De León, Andrés
AU - Demichelis-Gómez, Roberta
AU - Pinedo-Rodríguez, Alfredo
AU - Enriquez-Vera, Daniel
AU - Flores-Jiménez, Juan Antonio
AU - Ceballos-López, Adrián Alejandro
AU - Rodríguez-Mejorada, Margarita
AU - Herrera Riojas, Miguel Angel
AU - Ovilla-Martínez, Roberto
AU - Báez-Islas, Pamela
AU - Cota-Rangel, Xóchitl
AU - Neme-Yunes, Yvette
AU - Inclán-Alarcón, Sergio
AU - López-Flores, Nelson J.
AU - Colunga-Pedraza, Perla R.
AU - Rodríguez-Zúñiga, Anna C.
AU - Gómez-Almaguer, David
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Objectives: Venetoclax combinations are a new standard for patients with acute myeloid leukemia (AML). We aimed to evaluate the safety and efficacy of these combinations in a period of accelerated approval in Latin-America. Methods: This observational study evaluated adults with acute myeloid leukemia who received venetoclax-based therapy in 11 public or private centers in Mexico and Peru for both newly diagnosed or relapsed and refractory AML. Results: Fifty patients were included; 28 with newly diagnosed (ND) AML and 22 with relapsed/refractory (RR) disease. ND patients were older (64 vs. 40 years; p < 0.001) with a lower functional capacity (ECOG ≥2 64.3% vs 9%; p < 0.001). Venetoclax was frequently combined with azacytidine (60%) and prophylactic azoles (82%) with a median maximum dose of 200 mg (range, 100–600 mg). Hematologic toxicities were common. Complete response rates including patients with incomplete hematopoietic recovery were 78.6% in ND and 45.5% in RR patients, with a median overall survival of 9.6 (95% CI 3.7–15.5) and 8 months (95% CI 4.8–11.2). Discussion: Our study showed a preferred use of venetoclax plus azacytidine over cyatrabine. Patients in the first-line setting were similar to those in the landmark studies, while most patients with relapsed disease had received prior intensive therapies. Responses were favorable, with a median survival in agreement to other reports, albeit shorter than that observed in the randomized phase-3 trials. Conclusion: Venetoclax-based therapy in AML was effective despite dose reductions and prophylactic antifungals in two middle-income countries outside of a clinical trial setting.
AB - Objectives: Venetoclax combinations are a new standard for patients with acute myeloid leukemia (AML). We aimed to evaluate the safety and efficacy of these combinations in a period of accelerated approval in Latin-America. Methods: This observational study evaluated adults with acute myeloid leukemia who received venetoclax-based therapy in 11 public or private centers in Mexico and Peru for both newly diagnosed or relapsed and refractory AML. Results: Fifty patients were included; 28 with newly diagnosed (ND) AML and 22 with relapsed/refractory (RR) disease. ND patients were older (64 vs. 40 years; p < 0.001) with a lower functional capacity (ECOG ≥2 64.3% vs 9%; p < 0.001). Venetoclax was frequently combined with azacytidine (60%) and prophylactic azoles (82%) with a median maximum dose of 200 mg (range, 100–600 mg). Hematologic toxicities were common. Complete response rates including patients with incomplete hematopoietic recovery were 78.6% in ND and 45.5% in RR patients, with a median overall survival of 9.6 (95% CI 3.7–15.5) and 8 months (95% CI 4.8–11.2). Discussion: Our study showed a preferred use of venetoclax plus azacytidine over cyatrabine. Patients in the first-line setting were similar to those in the landmark studies, while most patients with relapsed disease had received prior intensive therapies. Responses were favorable, with a median survival in agreement to other reports, albeit shorter than that observed in the randomized phase-3 trials. Conclusion: Venetoclax-based therapy in AML was effective despite dose reductions and prophylactic antifungals in two middle-income countries outside of a clinical trial setting.
KW - Acute myeloid leukemia
KW - azacytidine
KW - BCL-2 inhibitor
KW - cytarabine
KW - venetoclax
UR - http://www.scopus.com/inward/record.url?scp=85125155190&partnerID=8YFLogxK
U2 - 10.1080/16078454.2021.2024940
DO - 10.1080/16078454.2021.2024940
M3 - Article
C2 - 35192778
AN - SCOPUS:85125155190
SN - 1024-5332
VL - 27
SP - 249
EP - 257
JO - Hematology (United Kingdom)
JF - Hematology (United Kingdom)
IS - 1
ER -