Grant Details
Grant Number: |
5R01CA069269-03 Interpret this number |
Primary Investigator: |
Melbye, Mads |
Organization: |
Statens Serum Institut |
Project Title: |
Determinants of the Secular Increase in Nhl |
Fiscal Year: |
2000 |
Abstract
DESCRIPTION: (Adapted from Investigator's Abstract) The investigators'
long-term objective is to make possible primary prevention of non-Hodgkin's
lymphoma (NHL), an increasingly common and often fatal cancer with an
etiology that is incompletely known. The specific aim is to investigate,
through a broad interdisciplinary collaboration, the etiologic role of
factors that entail immune modulation. The study will be large enough to
allow analyses of these factors separately for several distinct subgroups,
such as B-cell NHL, T-cell NHL, nodal/extranodal disease and chronic
lymphocytic leukemia (CLL). Conditions and exposures to be characterized in
detail include: Type-1 allergy, pattern and postponement of infection
during childhood, chronic infections, autoimmune diseases, UV-light
exposure, vaccinations, drugs that affect the immune system, and - notably
for T-cell lymphomas - exposure to EBV and other viruses. Drawing on
experience from nationwide collaborative studies between the major research
centers in Denmark and Sweden, they propose to conduct a large, nationwide,
population-based case-control study. A separate network for rapid case
ascertainment will be set up to identify all individuals aged 15-74 years
with a newly diagnosed, morphologically confirmed, and histopathologically
uniformly classified NHL or CLL. Population controls, frequency-matched to
the cases by sex, age, and country, will be regularly selected from
population registers. Following informed consent, a blood sample will be
obtained from all participants and a telephone interview will be carried out
by means of a structured questionnaire. Self-reported information will be
extensively completed and validated through linkages to national databases.
They anticipate an 80 percent or higher participation rate. During a
two-year period (two and a half years for T-cell NHL), they expect to
include at least 2,000 patients with B-cell NHL, 400 patients with T-cell
NHL, 525 patients with CLL, and approximately 3,000 population controls.
The investigators state that the large size enables them to detect, with 80%
power at a 5% level, factors that increase NHL by a factor of 1.3 or more
for B-cell NHLs, 1.5 or more for T-cell NHLs, and 1.5 or more for CLL at an
exposure prevalence of the risk factor in the general population of 1.5%.
Major subgroups within B-cell NHL can be analyzed with similar statistical
precision. The investigators state that the efficiency of the existing
infrastructure, the ready access to nationwide population-based databases,
the extensive previous experience with high participation rates, willingness
to provide blood samples, and ready access to histopathological specimens
provide a unique and effective platform in Scandinavia for such a large and
comprehensive study.
Publications
None