Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
05 08 2019
Historique:
received: 12 11 2018
accepted: 06 05 2019
entrez: 7 8 2019
pubmed: 7 8 2019
medline: 28 4 2020
Statut: epublish

Résumé

Chronic lymphocytic leukemia (CLL) and its precursor, monoclonal B-cell lymphocytosis (MBL), are heritable. Serumfree light-chain (sFLC) measures are a prognostic factor for CLL, but their role in susceptibility to CLL is not clear. We investigated differences between sFLC measurements in pre-treatment serum from five groups to inform the association of sFLC with familial and sporadic CLL: (1) familial CLL (n = 154), (2) sporadic CLL (n = 302), (3) familial MBL (n = 87), (4) unaffected first-degree relatives from CLL/MBL families (n = 263), and (5) reference population (n = 15,396). The percent of individuals having elevated monoclonal and polyclonal sFLCs was compared using age-stratified and age- and sex-adjusted logistic regression models. In age groups >50 years, monoclonal sFLC elevations were increased in sporadic and familial CLL cases compared to the reference population (p's < 0.05). However, there were no statistically significant differences in sFLC monoclonal or polyclonal elevations between familial and sporadic CLL cases (p's > 0.05). Unaffected relatives and MBL cases from CLL/MBL families, ages >60 years, showed elevated monoclonal sFLC, compared to the reference population (p's < 0.05). This is the first study to demonstrate monoclonal sFLC elevations in CLL cases compared to controls. Monoclonal sFLC levels may provide additional risk information in relatives of CLL probands.

Identifiants

pubmed: 31383849
doi: 10.1038/s41408-019-0220-x
pii: 10.1038/s41408-019-0220-x
pmc: PMC6683199
doi:

Substances chimiques

Biomarkers, Tumor 0
Immunoglobulin Light Chains 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

59

Subventions

Organisme : NCI NIH HHS
ID : R25 CA092049
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA092153
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014236
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA097274
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA134674
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA118444
Pays : United States

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Auteurs

Alyssa I Clay-Gilmour (AI)

Division of Epidemiology, Department of Health Sciences, Mayo Clinic, Rochester, MN, USA.

Abdul R Rishi (AR)

Department of Internal Medicine, Mercy Hospital, St. Louis, MO, USA.

Lynn R Goldin (LR)

Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.

Alexandra J Greenberg-Worisek (AJ)

Division of Epidemiology, Department of Health Sciences, Mayo Clinic, Rochester, MN, USA.

Sara J Achenbach (SJ)

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.

Kari G Rabe (KG)

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.

Matthew J Maurer (MJ)

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.

Neil E Kay (NE)

Division of Hematology, Mayo Clinic, Rochester, MN, 55905, USA.

Tait D Shanafelt (TD)

Stanford University Medical Center, Department of Medicine/Hematology, Stanford, CA, USA.

Timothy G Call (TG)

Division of Hematology, Mayo Clinic, Rochester, MN, 55905, USA.

J Brice Weinberg (J)

Duke University and V.A. Medical Centers, Durham, NC, USA.

Nicola J Camp (NJ)

Department of Medicine, University of Utah and Huntsman Cancer Institute, Salt Lake City, UT, USA.

James R Cerhan (JR)

Division of Epidemiology, Department of Health Sciences, Mayo Clinic, Rochester, MN, USA.

Jose Leis (J)

Division of Medical Oncology, Mayo Clinic, Phoenix, AZ, USA.

Aaron Norman (A)

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.

David L Murray (DL)

Laboratory Medicine and Pathology, College of Medicine, Mayo Clinic, Rochester, MN, 55905, USA.

S Vincent Rajkumar (S)

Division of Hematology, Mayo Clinic, Rochester, MN, 55905, USA.

Neil E Caporaso (NE)

Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.

Ola Landgren (O)

Myeloma Service, Division of Hematologic Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Mary L McMaster (ML)

Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.

Susan L Slager (SL)

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.

Celine M Vachon (CM)

Division of Epidemiology, Department of Health Sciences, Mayo Clinic, Rochester, MN, USA. vachon.celine@mayo.edu.

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Classifications MeSH