Dunia De Miguel

Dr. Dunia De Miguel


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2005 in Diagnostic Microbiology and Infectious Disease
Verified
Journal Article
Closed access
DMDunia De Miguel
Dunia De Miguel
PGPeña Gómez
Peña Gómez
RGRosa González
Rosa González
JGJulio García-Suárez
Julio García-Suárez
JCJuan Cuadros-González
Juan Cuadros-González
CBCarmen Burgaleta
Carmen Burgaleta

29 March 2022 in Cancers
Verified
Journal Article
Open access
PDF file
JLJorge Labrador
Jorge Labrador
MSMiriam Saiz-Rodríguez
Miriam Saiz-Rodríguez
DMDunia De Miguel
Dunia De Miguel
ALAlmudena De Laiglesia
Almudena De Laiglesia
CRCarlos Rodríguez-Medina
Carlos Rodríguez-Medina
PMPau Montesinos
Pau Montesinos
The effectiveness of venetoclax (VEN) in relapsed or refractory acute myeloid leukemia (RR-AML) has not been well established. This retrospective, multicenter, observational database studied the effectiveness of VEN in a cohort of 51 RR-AML patients and evaluated for predictors of response and overall survival (OS). The median age was 68 years, most were at high risk, 61% received ≥2 therapies for AML, 49% had received hypomethylating agents, and ECOG was ≥2 in 52%. Complete remission (CR) rate, including CR with incomplete hematological recovery (CRi), was 12.4%. Additionally, 10.4% experienced partial response (PR). The CR/CRi was higher in combination with azacitidine (AZA; 17.9%) than with decitabine (DEC; 6.7%) and low-dose cytarabine (LDAC; 0%). Mutated NPM1 was associated with increased CR/CRi. Median OS was 104 days (95% CI: 56–151). For the combination with AZA, DEC, and LDAC, median OS was 120 days, 104 days, and 69 days, respectively; p = 0.875. Treatment response and ECOG 0 influenced OS in a multivariate model. A total of 28% of patients required interruption of VEN because of toxicity. Our real-life series describes a marginal probability of CR/CRi and poor OS after VEN-based salvage. Patients included had very poor-risk features and were heavily pretreated. The small percentage of responders did not reach the median OS.