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

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作者
Alyssa I. Clay-Gilmour
Abdul R. Rishi
Lynn R. Goldin
Alexandra J. Greenberg-Worisek
Sara J. Achenbach
Kari G. Rabe
Matthew J. Maurer
Neil E. Kay
Tait D. Shanafelt
Timothy G. Call
J. Brice Weinberg
Nicola J. Camp
James R. Cerhan
Jose Leis
Aaron Norman
David L. Murray
S. Vincent Rajkumar
Neil E. Caporaso
Ola Landgren
Mary L. McMaster
Susan L. Slager
Celine M. Vachon
机构
[1] Mayo Clinic,Division of Epidemiology, Department of Health Sciences
[2] Mercy Hospital,Department of Internal Medicine
[3] Division of Cancer Epidemiology and Genetics,Division of Biomedical Statistics and Informatics, Department of Health Sciences Research
[4] National Cancer Institute (NCI),Department of Medicine
[5] National Institutes of Health (NIH),undefined
[6] Mayo Clinic,undefined
[7] Division of Hematology,undefined
[8] Mayo Clinic,undefined
[9] Stanford University Medical Center,undefined
[10] Department of Medicine/Hematology,undefined
[11] Duke University and V.A. Medical Centers,undefined
[12] University of Utah and Huntsman Cancer Institute,undefined
[13] Division of Medical Oncology,undefined
[14] Mayo Clinic,undefined
[15] Laboratory Medicine and Pathology,undefined
[16] College of Medicine,undefined
[17] Mayo Clinic,undefined
[18] Myeloma Service,undefined
[19] Division of Hematologic Oncology,undefined
[20] Memorial Sloan-Kettering Cancer Center,undefined
来源
Blood Cancer Journal | / 9卷
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摘要
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.
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