Association of Genomic Alterations with the Presence of Serum Monoclonal Proteins in Chronic Lymphocytic Leukemia

The presence of a monoclonal protein detected by serum immunofixation electrophoresis (sIFE) has been reported as an adverse prognostic factor in chronic lymphocytic leukemia (CLL). However, the genetic underpinning of this finding has not been studied. We retrospectively studied 97 CLL patients with simultaneous information on sIFE and genetic alterations detected by next-generation sequencing. sIFE was positive in 49 patients. The most common isotypes were IgG κ (27%) and bi/triclonal (25%). A +sIFE was associated with a higher number of mutated genes [median 2 (range 0-3) vs. 0 (range 0-2), <i>p</i> = 0.006], and a higher frequency of unmutated IGHV status (60 vs. 29%, <i>p</i> = 0.004). An IgM monoclonal protein was associated with <i>TP53</i> mutations (36% in IgM +sIFE vs. 12% in non-IgM +sIFE or -sIFE, <i>p</i> = 0.04), and bi/triclonal proteins with <i>NOTCH1</i> mutations (33% in bi/triclonal vs. 9% in monoclonal +sIFE or -sIFE, <i>p</i> = 0.04). These data suggest an association between a +sIFE and a higher mutational burden, and some monoclonal isotypes with specific mutations.

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Journal
Cells
Published
2024-11-07
DOI
https://doi.org/10.3390/cells13221839
Citations
2
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
0.88

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article

Association of Genomic Alterations with the Presence of Serum Monoclonal Proteins in Chronic Lymphocytic Leukemia

Nil Albiol, Mònica López‐Guerra, Julio Delgado, Neus Villamor et al.
2 citations
Cells
Chronic Lymphocytic Leukemia Research
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article

Association of Genomic Alterations with the Presence of Serum Monoclonal Proteins in Chronic Lymphocytic Leukemia

Nil Albiol, Mònica López‐Guerra, Julio Delgado, Neus Villamor, Elı́as Campo, Juan Gonzalo Correa, Marta Aymerich, Ferran Nadeu, Irene López‐Oreja, Pablo Mozas, Juan A. Piñeyroa, Juan I. Aróstegui, Dolors Costa, Aleix Borja Fabregat Bolufer, Sı́lvia Beà, Dolors Colomer, Ares Martínez-Farran, Ines Monge-Escatín
article en
2 citations

Abstract

The presence of a monoclonal protein detected by serum immunofixation electrophoresis (sIFE) has been reported as an adverse prognostic factor in chronic lymphocytic leukemia (CLL). However, the genetic underpinning of this finding has not been studied. We retrospectively studied 97 CLL patients with simultaneous information on sIFE and genetic alterations detected by next-generation sequencing. sIFE was positive in 49 patients. The most common isotypes were IgG κ (27%) and bi/triclonal (25%). A +sIFE was associated with a higher number of mutated genes [median 2 (range 0-3) vs. 0 (range 0-2), <i>p</i> = 0.006], and a higher frequency of unmutated IGHV status (60 vs. 29%, <i>p</i> = 0.004). An IgM monoclonal protein was associated with <i>TP53</i> mutations (36% in IgM +sIFE vs. 12% in non-IgM +sIFE or -sIFE, <i>p</i> = 0.04), and bi/triclonal proteins with <i>NOTCH1</i> mutations (33% in bi/triclonal vs. 9% in monoclonal +sIFE or -sIFE, <i>p</i> = 0.04). These data suggest an association between a +sIFE and a higher mutational burden, and some monoclonal isotypes with specific mutations.

CellsVol. 13(22)
Departament de Salut (ES), Hospital Clínic de Barcelona (ES), Centro de Investigación Biomédica en Red de Cáncer (ES), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES), Universitat de Barcelona (ES)
Centres de Recerca de Catalunya, Generalitat de Catalunya, Ministerio de Ciencia e Innovación, Instituto de Salud Carlos III, European Regional Development Fund
Good health and well-being
Openalex Percentile: Top 23%
Chronic Lymphocytic Leukemia Research
0.88
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