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Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia

INTRODUCTION: Combination of venetoclax and hypomethylating agents (HMAs) has become a standard of care in acute myeloid leukemia (AML) aged >75 years or who have comorbidities that preclude intensive induction chemotherapy. METHODS: We conducted a monocentric retrospective analysis on adult pati...

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Autores principales: Sciumè, Mariarita, Bosi, Alessandro, Canzi, Marta, Ceparano, Giusy, Serpenti, Fabio, De Roberto, Pasquale, Fabris, Sonia, Tagliaferri, Elena, Cavallaro, Francesca, Onida, Francesco, Fracchiolla, Nicola Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083332/
https://www.ncbi.nlm.nih.gov/pubmed/37051529
http://dx.doi.org/10.3389/fonc.2023.1149298
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author Sciumè, Mariarita
Bosi, Alessandro
Canzi, Marta
Ceparano, Giusy
Serpenti, Fabio
De Roberto, Pasquale
Fabris, Sonia
Tagliaferri, Elena
Cavallaro, Francesca
Onida, Francesco
Fracchiolla, Nicola Stefano
author_facet Sciumè, Mariarita
Bosi, Alessandro
Canzi, Marta
Ceparano, Giusy
Serpenti, Fabio
De Roberto, Pasquale
Fabris, Sonia
Tagliaferri, Elena
Cavallaro, Francesca
Onida, Francesco
Fracchiolla, Nicola Stefano
author_sort Sciumè, Mariarita
collection PubMed
description INTRODUCTION: Combination of venetoclax and hypomethylating agents (HMAs) has become a standard of care in acute myeloid leukemia (AML) aged >75 years or who have comorbidities that preclude intensive induction chemotherapy. METHODS: We conducted a monocentric retrospective analysis on adult patients affected by treatment-naïve AML not eligible for standard induction therapy or refractory/relapsed (R/R) AML treated with venetoclax combinations outside clinical trials. Venetoclax was administered at the dose of 400 mg/daily after a short ramp-up and reduced in case of concomitant CYP3A4 inhibitors. RESULTS: Sixty consecutive AML were identified. Twenty-three patients (38%) were affected by treatment-naïve AML and 37 (62%) by R/R AML. Median age was 70 years. Among R/R AML 30% had received a prior allogeneic stem cell transplantation (allo-HSCT). In combination with venetoclax, 50 patients (83%) received azacitidine. Antifungal prophylaxis was performed in 33 patients (55%). Overall response rate was 60%, with 53% of complete remission (CR; 78% for treatment-naïve and 49% for R/R, p 0.017). Median overall survival was 130 days for R/R patients and 269 days for treatment-naïve patients; median event free survival was 145 days for R/R cohort and 199 days for treatment-naïve AML. Measurable residual disease was negative in 26% of evaluable patients in CR/CR with incomplete hematologic recovery after 2 cycles and in 50% after 4 cycles, with no significant association with survival. Eleven patients (18%) received an allo-HSCT after venetoclax combinations. Most common grade 3/4 adverse events were infectious (51% of the patients), or hematological without infections (25% of the patients). Use of CYP3A4 inhibitors was associated with a trend to shorter cytopenias and with a lower rate of infections. Invasive fungal infections were less frequent among patients receiving azole prophylaxis (6% vs 26%; p 0.0659). DISCUSSION: Venetoclax-based regimens are a viable option for AML considered not eligible for standard induction therapy and a valid rescue therapy in the R/R setting. Azole prophylaxis did not significantly affect response and it was associated with a lower rate of invasive fungal infections. Despite a limited number of patients, the association of venetoclax and HMAs proved to be also a feasible bridging therapy to transplantation.
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spelling pubmed-100833322023-04-11 Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia Sciumè, Mariarita Bosi, Alessandro Canzi, Marta Ceparano, Giusy Serpenti, Fabio De Roberto, Pasquale Fabris, Sonia Tagliaferri, Elena Cavallaro, Francesca Onida, Francesco Fracchiolla, Nicola Stefano Front Oncol Oncology INTRODUCTION: Combination of venetoclax and hypomethylating agents (HMAs) has become a standard of care in acute myeloid leukemia (AML) aged >75 years or who have comorbidities that preclude intensive induction chemotherapy. METHODS: We conducted a monocentric retrospective analysis on adult patients affected by treatment-naïve AML not eligible for standard induction therapy or refractory/relapsed (R/R) AML treated with venetoclax combinations outside clinical trials. Venetoclax was administered at the dose of 400 mg/daily after a short ramp-up and reduced in case of concomitant CYP3A4 inhibitors. RESULTS: Sixty consecutive AML were identified. Twenty-three patients (38%) were affected by treatment-naïve AML and 37 (62%) by R/R AML. Median age was 70 years. Among R/R AML 30% had received a prior allogeneic stem cell transplantation (allo-HSCT). In combination with venetoclax, 50 patients (83%) received azacitidine. Antifungal prophylaxis was performed in 33 patients (55%). Overall response rate was 60%, with 53% of complete remission (CR; 78% for treatment-naïve and 49% for R/R, p 0.017). Median overall survival was 130 days for R/R patients and 269 days for treatment-naïve patients; median event free survival was 145 days for R/R cohort and 199 days for treatment-naïve AML. Measurable residual disease was negative in 26% of evaluable patients in CR/CR with incomplete hematologic recovery after 2 cycles and in 50% after 4 cycles, with no significant association with survival. Eleven patients (18%) received an allo-HSCT after venetoclax combinations. Most common grade 3/4 adverse events were infectious (51% of the patients), or hematological without infections (25% of the patients). Use of CYP3A4 inhibitors was associated with a trend to shorter cytopenias and with a lower rate of infections. Invasive fungal infections were less frequent among patients receiving azole prophylaxis (6% vs 26%; p 0.0659). DISCUSSION: Venetoclax-based regimens are a viable option for AML considered not eligible for standard induction therapy and a valid rescue therapy in the R/R setting. Azole prophylaxis did not significantly affect response and it was associated with a lower rate of invasive fungal infections. Despite a limited number of patients, the association of venetoclax and HMAs proved to be also a feasible bridging therapy to transplantation. Frontiers Media S.A. 2023-03-27 /pmc/articles/PMC10083332/ /pubmed/37051529 http://dx.doi.org/10.3389/fonc.2023.1149298 Text en Copyright © 2023 Sciumè, Bosi, Canzi, Ceparano, Serpenti, De Roberto, Fabris, Tagliaferri, Cavallaro, Onida and Fracchiolla https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Sciumè, Mariarita
Bosi, Alessandro
Canzi, Marta
Ceparano, Giusy
Serpenti, Fabio
De Roberto, Pasquale
Fabris, Sonia
Tagliaferri, Elena
Cavallaro, Francesca
Onida, Francesco
Fracchiolla, Nicola Stefano
Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title_full Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title_fullStr Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title_full_unstemmed Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title_short Real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
title_sort real-life monocentric experience of venetoclax-based regimens for acute myeloid leukemia
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083332/
https://www.ncbi.nlm.nih.gov/pubmed/37051529
http://dx.doi.org/10.3389/fonc.2023.1149298
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