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A Pilot Study of Non-Hodgkin's Lymphoma: Chemotherapy and Blood Levels of Organochlorines


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Not Enrolling
Both
HIV Infections, Lymphoma, AIDS-Related, Lymphoma, Non-Hodgkin

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Trial Information

A Pilot Study of Non-Hodgkin's Lymphoma: Chemotherapy and Blood Levels of Organochlorines


Non-Hodgkin's lymphoma (NHL) is the third most rapidly increasing cancer in the United
States. HIV-related NHL is responsible for some of the increase since the early 1980s.
However, it cannot explain the steady increase in the incidence rates in earlier years, nor
the entire increase shown recently. A possible role of environmental exposures is receiving
attention. One possibility is that exposure to organochlorines (OCs) may be related to the
occurrence of NHL. NCI is currently designing a large population-based case-control study
to investigate this hypothesis further by analyzing OC levels in blood collected at the time
of interview from cases of NHL and their matched controls. At the time of these interviews,
cases in the main case-control study would most likely have already received chemotherapy.
If chemotherapy changes the blood levels of OCs, this may lead to misclassification of
exposure among cases and eventually to biased risk estimates. The purpose of this pilot
study is to estimate the bias due to measuring the serum levels of OCs in cases during or
after chemotherapy. Twenty newly diagnosed patients will be recruited for the study. From
each patient, four consecutive blood samples, one prior to, two during, and one after
chemotherapy, will be collected. Forty pairs of pre-existing cryopreserved serum samples
(pre- and post-treatment) taken from the NHL patients who participated in an earlier NCI
clinical study will also be included in this study. Samples will be assayed for OC levels.
The results will be used to plan and to interpret another large case-control study (the main
study).

Inclusion Criteria


All NHL patients who have not previously received chemotherapy and who are admitted to the
NCI Clinical Center to be enrolled in trails will be eligible for the study.

All histological subtypes and stages.

Any NHL patient who is between the ages of 20 and 74.

Must be able to give informed consent.

No NHL patient HIV positive will be included.

Type of Study:

Observational

Study Design:

N/A

Authority:

United States: Federal Government

Study ID:

970075

NCT ID:

NCT00001571

Start Date:

February 1997

Completion Date:

December 2000

Related Keywords:

  • HIV Infections
  • Lymphoma, AIDS-Related
  • Lymphoma, Non-Hodgkin
  • Cancer
  • DDT, PCB
  • Epidemiology
  • Pesticides
  • Serum
  • HIV Infections
  • Acquired Immunodeficiency Syndrome
  • Lymphoma
  • Lymphoma, Non-Hodgkin
  • Lymphoma, AIDS-Related

Name

Location

National Cancer Institute (NCI) Bethesda, Maryland  20892