Literature DB >> 33122345

Mutational Landscape and Tumor Burden Assessed by Cell-free DNA in Diffuse Large B-Cell Lymphoma in a Population-Based Study.

Alfredo Rivas-Delgado1,2,3, Ferran Nadeu2,4, Eva Giné5,2,4, Armando López-Guillermo5,2,3,4, Anna Enjuanes2,4, Sebastián Casanueva-Eliceiry6, Pablo Mozas5,2, Laura Magnano5,2, Natalia Castrejón de Anta7, Jordina Rovira5, Ivan Dlouhy5, Silvia Martín2,3, Miguel Osuna7, Sonia Rodríguez8, Marc Simó9, Magda Pinyol2,4, Tycho Baumann5,2,4, Silvia Beà2,3,4, Olga Balagué2,3,4,7, Julio Delgado5,2,3,4, Neus Villamor2,4,7, Xavier Setoain2,6,10, Elías Campo2,3,4,7.   

Abstract

PURPOSE: We analyzed the utility of cell-free DNA (cfDNA) in a prospective population-based cohort to determine the mutational profile, assess tumor burden, and estimate its impact in response rate and outcome in patients with diffuse large B-cell lymphoma (DLBCL). EXPERIMENTAL
DESIGN: A total of 100 patients were diagnosed with DLBCL during the study period. Mutational status of 112 genes was studied in cfDNA by targeted next-generation sequencing. Paired formalin-fixed, paraffin-embedded samples and volumetric PET/CT were assessed when available.
RESULTS: Appropriate cfDNA to perform the analyses was obtained in 79 of 100 cases. At least one mutation could be detected in 69 of 79 cases (87%). The sensitivity of cfDNA to detect the mutations was 68% (95% confidence interval, 56.2-78.7). The mutational landscape found in cfDNA samples was highly consistent with that shown in the tissue and allowed genetic classification in 43% of the cases. A higher amount of circulating tumor DNA (ctDNA) significantly correlated with clinical parameters related to tumor burden (elevated lactate dehydrogenase and β2-microglobulin serum levels, advanced stage, and high-risk International Prognostic Index) and total metabolic tumor volume assessed by PET/CT. In patients treated with curative intent, high ctDNA levels (>2.5 log hGE/mL) were associated with lower complete response (65% vs. 96%; P < 0.004), shorter progression-free survival (65% vs. 85%; P = 0.038), and overall survival (73% vs. 100%; P = 0.007) at 2 years, although it did not maintain prognostic value in multivariate analyses.
CONCLUSIONS: In a population-based prospective DLBCL series, cfDNA resulted as an alternative source to estimate tumor burden and to determine the tumor mutational profile and genetic classification, which have prognostic implications and may contribute to a future tailored treatment. ©2020 American Association for Cancer Research.

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Year:  2020        PMID: 33122345     DOI: 10.1158/1078-0432.CCR-20-2558

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  12 in total

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Review 5.  Advances in Multi-Omics Study of Prognostic Biomarkers of Diffuse Large B-Cell Lymphoma.

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Review 6.  The Minimal Residual Disease Using Liquid Biopsies in Hematological Malignancies.

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7.  Cell-Free DNA for Genomic Analysis in Primary Mediastinal Large B-Cell Lymphoma.

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9.  TP53-Mutated Circulating Tumor DNA for Disease Monitoring in Lymphoma Patients after CAR T Cell Therapy.

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Review 10.  How to Obtain a High Quality ctDNA in Lymphoma Patients: Preanalytical Tips and Tricks.

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