Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010 Jul;17(4):350-5.
doi: 10.1097/MOH.0b013e328338cd99.

Familial chronic lymphocytic leukemia

Affiliations
Review

Familial chronic lymphocytic leukemia

Lynn R Goldin et al. Curr Opin Hematol. 2010 Jul.

Abstract

Purpose of review: Families with multiple individuals affected with chronic lymphocytic leukemia (CLL) and other related B-cell tumors have been described in the literature and strong familial aggregation has been seen in population studies. However, predisposing germline mutations have not been identified. We will discuss the spectrum of conditions associated with CLL in families and the advances in identifying the underlying susceptibility genes.

Recent findings: Familial CLL does not appear to differ substantially from sporadic CLL in terms of prognostic markers and clinical outcome, although it may be associated with more indolent disease. The precursor condition, monoclonal B-cell lymphocytosis, also aggregates in CLL families. Linkage studies have been conducted in high-risk CLL families to screen the whole genome for susceptibility loci but no gene mutations have yet been identified by this method. Association studies of candidate genes have implicated several genes as being important in CLL but more studies are needed. Results from whole-genome association studies are promising.

Summary: The ability to conduct large-scale genomic studies in unrelated CLL patients and in high-risk CLL families will play an important role in detecting susceptibility genes for CLL over the next few years and thereby help to delineate causal pathways.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Pedigree with multiple cases of CLL as well as the precursor, MBL
Figure 2
Figure 2. Pedigree with both CLL and WM cases, as well as the precursor MGUS
Reproduced with permission Lynn R. Goldin, Ola Landgren, Gerald E. Marti, Neil E. Caporaso, Familial aspects of chronic lymphocytic leukemia, monoclonal b-cell lymphocytosis, and related lymphomas, European Journal of Clinical and Medical Oncology, 2009

References

    1. Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ. Cancer statistics, 2009. CA Cancer J Clin. 2009;59:225–249. - PubMed
    1. Jaffe ES, Harris NL, Stein H, Isaacson PG. Classification of lymphoid neoplasms: the microscope as a tool for disease discovery. Blood. 2008;112:4384–4399. - PMC - PubMed
    1. Horner MJ, Ries LAG, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2006. National Cancer Institute; Bethesda, MD: 2009.
    1. Linet MS, Schubauer-Berigan MK, Weisenburger DD, et al. Chronic lymphocytic leukaemia: an overview of aetiology in light of recent developments in classification and pathogenesis. Br J Haematol. 2007;139:672–686. - PubMed
    1. Houlston RS, Sellick G, Yuille M, Matutes E, Catovsky D. Causation of chronic lymphocytic leukemia--insights from familial disease. Leuk Res. 2003;27:871–876. - PubMed

Publication types