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No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group

Gemtuzumab ozogamicin (GO) is a conjugate of a monoclonal antibody and calicheamicin, which has been reapproved for the treatment of acute myeloid leukemia (AML). AML patients with the CD33 rs12459419 CC genotype might benefit from the addition of GO to intensive treatment in contrast to patients wi...

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Autores principales: Castaño-Bonilla, Tamara, Barragán, Eva, Sargas, Claudia, Sanz, Alejandro, Algarra, Lorenzo, Herrera-Puente, Pilar, García-Boyero, Raimundo, Barrios, Manuel, Martinez-Cuadron, David, Rodriguez-Veiga, Rebeca, Boluda, Blanca, Gil, Cristina, Serrano-López, Josefina, Martínez-López, Joaquín, Sayas-Lloris, María José, Olave, María Teresa, Riaza-Grau, Rosalía, Castillo, Teresa Bernal-Del, Larrayoz, María José, Amigo, Raquel, Jiménez-Velasco, Antonio, Sánchez, Joaquín, Ayala, Rosa, Blas, Carlos, Lainez, Daniel, Serrano-López, Juana, Sanz, Miguel A., Alonso-Domínguez, Juan M., Montesinos, Pau
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427256/
https://www.ncbi.nlm.nih.gov/pubmed/36051360
http://dx.doi.org/10.1155/2022/3132941
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author Castaño-Bonilla, Tamara
Barragán, Eva
Sargas, Claudia
Sanz, Alejandro
Algarra, Lorenzo
Herrera-Puente, Pilar
García-Boyero, Raimundo
Barrios, Manuel
Martinez-Cuadron, David
Rodriguez-Veiga, Rebeca
Boluda, Blanca
Gil, Cristina
Serrano-López, Josefina
Martínez-López, Joaquín
Sayas-Lloris, María José
Olave, María Teresa
Riaza-Grau, Rosalía
Castillo, Teresa Bernal-Del
Larrayoz, María José
Amigo, Raquel
Jiménez-Velasco, Antonio
Sánchez, Joaquín
Ayala, Rosa
Blas, Carlos
Lainez, Daniel
Serrano-López, Juana
Sanz, Miguel A.
Alonso-Domínguez, Juan M.
Montesinos, Pau
author_facet Castaño-Bonilla, Tamara
Barragán, Eva
Sargas, Claudia
Sanz, Alejandro
Algarra, Lorenzo
Herrera-Puente, Pilar
García-Boyero, Raimundo
Barrios, Manuel
Martinez-Cuadron, David
Rodriguez-Veiga, Rebeca
Boluda, Blanca
Gil, Cristina
Serrano-López, Josefina
Martínez-López, Joaquín
Sayas-Lloris, María José
Olave, María Teresa
Riaza-Grau, Rosalía
Castillo, Teresa Bernal-Del
Larrayoz, María José
Amigo, Raquel
Jiménez-Velasco, Antonio
Sánchez, Joaquín
Ayala, Rosa
Blas, Carlos
Lainez, Daniel
Serrano-López, Juana
Sanz, Miguel A.
Alonso-Domínguez, Juan M.
Montesinos, Pau
author_sort Castaño-Bonilla, Tamara
collection PubMed
description Gemtuzumab ozogamicin (GO) is a conjugate of a monoclonal antibody and calicheamicin, which has been reapproved for the treatment of acute myeloid leukemia (AML). AML patients with the CD33 rs12459419 CC genotype might benefit from the addition of GO to intensive treatment in contrast to patients with CT/TT genotypes. Nevertheless, contradictory results have been reported. We sought to shed light on the prediction of GO response in AML patients with rs12459419 polymorphism who were treated with GO in the consolidation (n = 70) or reinduction (n = 20) phase. The frequency distribution of the rs12459419 polymorphism in the complete cohort of patients was 44.4% (n = 40), 50% (n = 45), and 5.6% (n = 5) for CC, CT, and TT genotypes, respectively. Regarding the patients treated with GO for consolidation, we performed a Kaplan-Meier analysis of overall survival and relapse-free survival according to the rs12459419 polymorphism (CC vs. CT/TT patients) and genetic risk using the European Leukemia Net (ELN) 2010 risk score. We also carried out a Cox regression analysis for the prediction of overall survival, with age and ELN 2010 as covariates. We found no statistical significance in the univariate or multivariate analysis. Additionally, we performed a global Kaplan-Meier analysis for the patients treated with GO for reinduction and did not find significant differences; however, our cohort was too small to draw any conclusion from this analysis. The use of GO in consolidation treatment is included in the approval of the compound; however, evidence regarding its efficacy in this setting is lacking. Rs12459419 polymorphism could help in the selection of patients who might benefit from GO. Regrettably, in our cohort, the rs12459419 polymorphism does not seem to be an adequate tool for the selection of patients who might benefit from the addition of GO in consolidation cycles.
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spelling pubmed-94272562022-08-31 No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group Castaño-Bonilla, Tamara Barragán, Eva Sargas, Claudia Sanz, Alejandro Algarra, Lorenzo Herrera-Puente, Pilar García-Boyero, Raimundo Barrios, Manuel Martinez-Cuadron, David Rodriguez-Veiga, Rebeca Boluda, Blanca Gil, Cristina Serrano-López, Josefina Martínez-López, Joaquín Sayas-Lloris, María José Olave, María Teresa Riaza-Grau, Rosalía Castillo, Teresa Bernal-Del Larrayoz, María José Amigo, Raquel Jiménez-Velasco, Antonio Sánchez, Joaquín Ayala, Rosa Blas, Carlos Lainez, Daniel Serrano-López, Juana Sanz, Miguel A. Alonso-Domínguez, Juan M. Montesinos, Pau Dis Markers Research Article Gemtuzumab ozogamicin (GO) is a conjugate of a monoclonal antibody and calicheamicin, which has been reapproved for the treatment of acute myeloid leukemia (AML). AML patients with the CD33 rs12459419 CC genotype might benefit from the addition of GO to intensive treatment in contrast to patients with CT/TT genotypes. Nevertheless, contradictory results have been reported. We sought to shed light on the prediction of GO response in AML patients with rs12459419 polymorphism who were treated with GO in the consolidation (n = 70) or reinduction (n = 20) phase. The frequency distribution of the rs12459419 polymorphism in the complete cohort of patients was 44.4% (n = 40), 50% (n = 45), and 5.6% (n = 5) for CC, CT, and TT genotypes, respectively. Regarding the patients treated with GO for consolidation, we performed a Kaplan-Meier analysis of overall survival and relapse-free survival according to the rs12459419 polymorphism (CC vs. CT/TT patients) and genetic risk using the European Leukemia Net (ELN) 2010 risk score. We also carried out a Cox regression analysis for the prediction of overall survival, with age and ELN 2010 as covariates. We found no statistical significance in the univariate or multivariate analysis. Additionally, we performed a global Kaplan-Meier analysis for the patients treated with GO for reinduction and did not find significant differences; however, our cohort was too small to draw any conclusion from this analysis. The use of GO in consolidation treatment is included in the approval of the compound; however, evidence regarding its efficacy in this setting is lacking. Rs12459419 polymorphism could help in the selection of patients who might benefit from GO. Regrettably, in our cohort, the rs12459419 polymorphism does not seem to be an adequate tool for the selection of patients who might benefit from the addition of GO in consolidation cycles. Hindawi 2022-08-23 /pmc/articles/PMC9427256/ /pubmed/36051360 http://dx.doi.org/10.1155/2022/3132941 Text en Copyright © 2022 Tamara Castaño-Bonilla et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Castaño-Bonilla, Tamara
Barragán, Eva
Sargas, Claudia
Sanz, Alejandro
Algarra, Lorenzo
Herrera-Puente, Pilar
García-Boyero, Raimundo
Barrios, Manuel
Martinez-Cuadron, David
Rodriguez-Veiga, Rebeca
Boluda, Blanca
Gil, Cristina
Serrano-López, Josefina
Martínez-López, Joaquín
Sayas-Lloris, María José
Olave, María Teresa
Riaza-Grau, Rosalía
Castillo, Teresa Bernal-Del
Larrayoz, María José
Amigo, Raquel
Jiménez-Velasco, Antonio
Sánchez, Joaquín
Ayala, Rosa
Blas, Carlos
Lainez, Daniel
Serrano-López, Juana
Sanz, Miguel A.
Alonso-Domínguez, Juan M.
Montesinos, Pau
No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title_full No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title_fullStr No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title_full_unstemmed No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title_short No Evidence that CD33 rs12459419 Polymorphism Predicts Gemtuzumab Ozogamicin Response in Consolidation Treatment of Acute Myeloid Leukemia Patients: Experience of the PETHEMA Group
title_sort no evidence that cd33 rs12459419 polymorphism predicts gemtuzumab ozogamicin response in consolidation treatment of acute myeloid leukemia patients: experience of the pethema group
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427256/
https://www.ncbi.nlm.nih.gov/pubmed/36051360
http://dx.doi.org/10.1155/2022/3132941
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