Publication:
Venetoclax-based combinations for acute myeloid leukemia: optimizing their use in Latin-America

dc.contributor.authorGómez-De León, A
dc.contributor.authorDemichelis-Gómez, R
dc.contributor.authorPinedo-Rodríguez, A
dc.contributor.authorEnriquez-Vera, D
dc.contributor.authorFlores-Jiménez, JA
dc.contributor.authorCeballos-López, AA
dc.contributor.authorRodríguez-Mejorada, M
dc.contributor.authorHerrera Riojas, MA
dc.contributor.authorOvilla-Martínez, R
dc.contributor.authorBáez-Islas, P
dc.contributor.authorCota-Rangel, X
dc.contributor.authorNeme-Yunes, Y
dc.contributor.authorInclán-Alarcón, S
dc.contributor.authorLópez-Flores, NJ
dc.contributor.authorColunga-Pedraza, PR
dc.contributor.authorRodríguez-Zúñiga, AC
dc.contributor.authorGómez-Almaguer, D
dc.date.accessioned2025-01-02T14:42:50Z
dc.date.available2025-01-02T14:42:50Z
dc.date.issued2022
dc.description.abstractObjectives: 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
dc.description.abstract28 with newly diagnosed (ND) AML and 22 with relapsed/refractory (RR) disease. ND patients were older (64 vs. 40 years
dc.description.abstractp < 0.001) with a lower functional capacity (ECOG ≥2 64.3% vs 9%
dc.description.abstractp < 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.
dc.formatapplication/pdf
dc.identifier.doihttps: //doi.org/10.1080/16078454.2021.2024940
dc.identifier.journalHematology (United Kingdom)
dc.identifier.urihttps://hdl.handle.net/20.500.14703/337
dc.language.isoeng
dc.publisherTaylor and Francis Ltd.
dc.publisher.countryUK
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectAcute myeloid leukemia
dc.subjectazacytidine
dc.subjectBCL-2 inhibitor
dc.subjectcytarabine
dc.subjectvenetoclax
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.21
dc.titleVenetoclax-based combinations for acute myeloid leukemia: optimizing their use in Latin-America
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication

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