Characterizing the Mutational Landscape of Diffuse Large B-Cell Lymphoma in a Prospective Cohort of Mexican Patients

Author:

Candelaria Myrna1ORCID,Cerrato-Izaguirre Dennis2ORCID,Gutierrez Olga1,Diaz-Chavez Jose2ORCID,Aviles Alejandro3ORCID,Dueñas-Gonzalez Alfonso4,Malpica Luis5

Affiliation:

1. Clinical Research, The National Cancer Institute, Ciudad de Mexico 14080, Mexico

2. Basic Research Division, Instituto Nacional de Cancerología, Ciudad de Mexico 14080, Mexico

3. Pathology Department, Instituto Nacional de Cancerología, Ciudad de Mexico 14080, Mexico

4. Unidad de Investigación Biomédica en Cancer, Instituto Nacional de Cancerología, Ciudad de Mexico 14080, Mexico

5. Department of Lymphoma/Myeloma, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common B-cell malignancy worldwide. Molecular classifications have tried to improve cure rates. We prospectively examined and correlated the mutational landscape with the clinical features and outcomes of 185 Mexican patients (median age 59.3 years, 50% women) with newly diagnosed DLBCL. A customized panel of 79 genes was designed, based on previous international series. Most patients had ECOG performance status (PS) < 2 (69.2%), advanced-stage disease (72.4%), germinal-center phenotype (68.1%), and double-hit lymphomas (14.1%). One hundred and ten (59.5%) patients had at least one gene with driver mutations. The most common mutated genes were as follows: TP53, EZH2, CREBBP, NOTCH1, and KMT2D. The median follow-up was 42 months, and the 5-year relapse-free survival (RFS) and overall survival (OS) rates were 70% and 72%, respectively. In the multivariate analysis, both age > 50 years and ECOG PS > 2 were significantly associated with a worse OS. Our investigation did not reveal any discernible correlation between the presence of a specific mutation and survival. In conclusion, using a customized panel, we characterized the mutational landscape of a large cohort of Mexican DLBCL patients. These results need to be confirmed in further studies.

Publisher

MDPI AG

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