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Blood, 24 September 2009, Vol. 114, No. 13, pp. 2730-2732. Prepublished online as a Blood First Edition Paper on July 28, 2009; DOI 10.1182/blood-2009-04-217521.
LYMPHOID NEOPLASIA A prospective study of serum soluble CD30 concentration and risk of non-Hodgkin lymphoma1 Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, US Department of Health and Human Services, Bethesda, MD; 2 Departments of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles; 3 Department of Medicine, University of Minnesota, Minneapolis; 4 Department of Hematology/Oncology, Marshfield Clinic, WI; and 5 Protein Expression Laboratory, Advanced Technology Program, SAIC-Frederick Inc, National Cancer Institute, Frederick, MD Prediagnostic serum concentration of soluble CD30 (sCD30), a marker for chronic B-cell stimulation, has been associated with increased risk of developing AIDS-related non-Hodgkin lymphoma (NHL) in a recent study of HIV+ patients. To investigate among healthy persons whether serum sCD30 is associated with NHL risk, we carried out a nested case-control study within the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial. There was a strong dose-response relationship between prediagnostic sCD30 concentration and NHL risk among 234 cases and 234 individually matched controls (odds ratio [95% confidence interval] for second, third, and fourth quartiles vs first quartile: 1.4 [0.8-2.6], 2.2 [1.2-4.1], 4.1 [2.2-7.8]; Ptrend < .001), which persisted among cases diagnosed 6 to 10 years after providing a blood sample. Given that a similar relationship has been observed among HIV+ patients, our findings suggest that chronic B-cell stimulation may be an important mechanism involved in B-cell lymphomagenesis among severely immunocompromised and healthy populations alike.
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