A prospective study of serum soluble CD30 concentration and risk of non-Hodgkin lymphoma

Author:

Purdue Mark P.1,Lan Qing1,Martinez-Maza Otoniel2,Oken Martin M.3,Hocking William4,Huang Wen-Yi1,Baris Dalsu1,Conde Betty5,Rothman Nathaniel1

Affiliation:

1. 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

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference14 articles.

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